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Juha Kere

Research Profile

Physiology

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Finland

Genes & Molecular Sequences

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Chromosomes, Human, Pair 7

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B I Nwaru; Juha Pekkanen; Olli Simell; H-M Takkinen; H Tuomi; Riitta Veijola; Suvi Ahonen; Maijaliisa Erkkola; Anna-Maija Haapala; Heikki Hyöty; Jorma Ilonen; Minna Kaila; Mike Kenward; Juha Kere; Mikael Knip; Riitta Lahesmaa; Onni Niemelä; Suvi M Virtanen
Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort.
Kristiina Tammimies; Morana Vitezic; Thomas R Bürglin; Carsten O Daub; Juha Kere; Sylvie Le Guyader; Hans Matsson; Tuula A Nyman; Tiina Ohman; Staffan Strömblad; Isabel Tapia-Páez
Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins.
Yun Liu; Leonid Padyukov; Lovisa Reinius; Marcus Ronninger; Arni Runarsson; Annika Scheynius; Klementy Shchetynsky; Margaret Taub; Nathalie Acevedo; Lars Alfredsson; Martin Aryee; Tomas J Ekström; MARGARET D FALLIN; Espen Hesselberg; Juha Kere; Lars Klareskog; Andrew P Feinberg
Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis.

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All Publications

2013: B I Nwaru; Juha Pekkanen; Olli Simell; H-M Takkinen; H Tuomi; Riitta Veijola; Suvi Ahonen; Maijaliisa Erkkola; Anna-Maija Haapala; Heikki Hyöty; Jorma Ilonen; Minna Kaila; Mike Kenward; Juha Kere; Mikael Knip; Riitta Lahesmaa; Onni Niemelä; Suvi M Virtanen
Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort.
Allergy 2013;68(4):507-16.
2013: Kristiina Tammimies; Morana Vitezic; Thomas R Bürglin; Carsten O Daub; Juha Kere; Sylvie Le Guyader; Hans Matsson; Tuula A Nyman; Tiina Ohman; Staffan Strömblad; Isabel Tapia-Páez
Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteins.
Biological psychiatry 2013;73(6):583-90.
2013: Yun Liu; Leonid Padyukov; Lovisa Reinius; Marcus Ronninger; Arni Runarsson; Annika Scheynius; Klementy Shchetynsky; Margaret Taub; Nathalie Acevedo; Lars Alfredsson; Martin Aryee; Tomas J Ekström; MARGARET D FALLIN; Espen Hesselberg; Juha Kere; Lars Klareskog; Andrew P Feinberg
Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis.
Nature biotechnology 2013;31(2):142-7.
2013: Gayathri Chandrasekar; Kjell Hultenby; Isabel Tapia-Páez; Liselotte Vesterlund; Juha Kere
The Zebrafish Orthologue of the Dyslexia Candidate Gene DYX1C1 Is Essential for Cilia Growth and Function.
PloS one 2013;8(5):e63123.
2013: Nathalie Acevedo; Harri Alenius; Charlotte Braun-Fahrländer; Mauro D'Amato; Gert Doekes; Sini Ezer; Gustav Boije Af Gennäs; Piia Karisola; Juha Kere; Jami Mandelin; Erik Melén; Göran Pershagen; Christina Orsmark Pietras; Josef Riedler; A Sääf; Annika Scheynius; Cilla Söderhäll; Marianne van Hage; Johanna Vendelin; Erika von Mutius; Jari Yli-Kauhaluoma; Ville Pulkkinen
Interaction between Retinoid Acid Receptor-Related Orphan Receptor Alpha (RORA) and Neuropeptide S Receptor 1 (NPSR1) in Asthma.
PloS one 2013;8(4):e60111.
2013: Katariina Hannula-Jouppi; Hong Jiao; Matti Karppelin; Katja Kivinen; Rasko Leinonen; Siru Mäkelä; Satu Massinen; Tuula Siljander; Jaana Syrjänen; Jaana Vuopio; Päivi Aitos; Juha Kere
Genetic susceptibility to non-necrotizing erysipelas/cellulitis.
PloS one 2013;8(2):e56225.
2013: Lovisa E Reinius; A Sääf; Annika Scheynius; Cilla Söderhäll; Nathalie Acevedo; Anna Bergström; Sven-Erik Dahlén; Mauro D'Amato; Anna Gref; Maaike Joerink; Maciej Kupczyk; Erik Melén; Göran Pershagen; Juha Kere
DNA methylation in the Neuropeptide S Receptor 1 (NPSR1) promoter in relation to asthma and environmental factors.
PloS one 2013;8(1):e53877.
2013: Bright I Nwaru; Juha Pekkanen; Olli Simell; Hanna-Mari Takkinen; Riitta Veijola; Suvi Ahonen; Maijaliisa Erkkola; Anna-Maija Haapala; Heikki Hyöty; Jorma Ilonen; Minna Kaila; Mike Kenward; Juha Kere; Mikael Knip; Riitta Lahesmaa; Onni Niemelä; Suvi M Virtanen
Timing of infant feeding in relation to childhood asthma and allergic diseases.
The Journal of allergy and clinical immunology 2013;131(1):78-86.
2012: Marco Zucchelli; Frida Holm; Outi Hovatta; Juha Kere; Helena Malmgren; Piotr Religa; Sigrid Sahlén; Susanne Ström; José Inzunza
In vivo differentiated human embryonic stem cells can acquire chromosomal aberrations more frequently than in vitro during the same period.
Stem cells and development 2012;21(18):3363-71.
2012: Lena Hafrén; Erna Kentala; Juha Kere; Elisabet Einarsdottir; Petri S Mattila
Current knowledge of the genetics of otitis media.
Current allergy and asthma reports 2012;12(6):582-9.
2012: Hanna Renvall; Elina Salmela; Mia Illman; Juha Kere; Eira Leinonen; Minna Vihla; Riitta Salmelin
Genome-wide linkage analysis of human auditory cortical activation suggests distinct loci on chromosomes 2, 3, and 8.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012;32(42):14511-8.
2012: Fahimeh Darki; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Torkel Klingberg
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.
Biological psychiatry 2012;72(8):671-6.
2012: Gisela G G Slaats; Johan S Alm; Juha Kere; Lovisa E Reinius; Annika Scheynius; Maaike Joerink
DNA methylation levels within the CD14 promoter region are lower in placentas of mothers living on a farm.
Allergy 2012;67(7):895-903.
2012: Stina Söderqvist; Sissela Bergman Nutley; Keith Humphreys; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Torkel Klingberg
Dopamine, working memory, and training induced plasticity: implications for developmental research.
Developmental psychology 2012;48(3):836-43.
2012: Kristiina Tammimies; Isabel Tapia-Páez; Jan-Åke Gustafsson; Juha Kere; Gustaf Rosin; Joëlle Rüegg; Ivan Nalvarte
The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.
Molecular endocrinology (Baltimore, Md.) 2012;26(4):619-29.
2012: Ville Pulkkinen; Kaisa Salmenkivi; Eva Sutinen; Heli Piiparinen; Maija Halme; Ulla Hodgson; Anne J Jääskeläinen; Juha Kere; Vuokko L Kinnula; Maija Lappalainen; Irmeli Lautenschlager; Juho T Lehto; Marjukka Myllärniemi
A novel screening method detects herpesviral DNA in the idiopathic pulmonary fibrosis lung.
Annals of medicine 2012;44(2):178-86.
2012: Satu Lamminmäki; Satu Massinen; Jaana Nopola-Hemmi; Juha Kere; Riitta Hari
Human ROBO1 regulates interaural interaction in auditory pathways.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2012;32(3):966-71.
2012: Thomas Scerri; John Stein; Joel B Talcott; Andrew J O Whitehouse; Craig E Pennell; Myriam Peyrard-Janvid; Susan Ring; Qi W Ang; Fahimeh Darki; Juha Kere; Torkel Klingberg; Hans Matsson; Anthony P Monaco; Andrew P Morris; Dianne F Newbury; Silvia Paracchini
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
PloS one 2012;7(11):e50321.
2012: Mari H Tervaniemi; Inkeri Tiala; Jyrki Vuola; Juha Kere; Gurinder Minhas; Lena Samuelsson; H Annika Siitonen; Cilla Söderhäll; Raija Sormunen; Sari Suomela; Outi Elomaa
Centrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organization.
PloS one 2012;7(11):e49920.
2012: Lovisa E Reinius; Annika Scheynius; Cilla Söderhäll; Göran Pershagen; Nathalie Acevedo; Sven-Erik Dahlén; Dario Greco; Maaike Joerink; Juha Kere
Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility.
PloS one 2012;7(7):e41361.
2012: Matthew P Johnson; Eero Kajantie; Jack W Kent; Juha Kere; Katja Kivinen; Hannele Laivuori; Anneli Pouta; Linda T Roten; Joanne M Said; Lawrence J Abraham; Rigmor Austgulen; John C Blangero; Shaun P Brennecke; Thomas D Dyer; Christine E East; Harald H H Göring; Seppo Heinonen; Ann-Charlotte Iversen; Eric K Moses
Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.
PloS one 2012;7(3):e33666.
2012: Gustaf Rosin; Linda Lindström; Jonas Bergh; Per Hall; Ulf Hannelius; Johan Hartman; Juha Kere
The dyslexia candidate gene DYX1C1 is a potential marker of poor survival in breast cancer.
BMC cancer 2012;12():79.
2011: Jari Lahti; Anu-Katriina Pesonen; Katri Räikkönen; Anna Rautanen; Kristian Wahlbeck; Sara Bruce; Kati Heinonen; Eero Kajantie; Juha Kere; Johan G Eriksson
Glucocorticoid receptor gene haplotype predicts increased risk of hospital admission for depressive disorders in the Helsinki birth cohort study.
Journal of psychiatric research 2011;45(9):1160-4.
2011: Iroise Dumontheil; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Chantal Roggeman; Tim Ziermans; Torkel Klingberg
Influence of the COMT genotype on working memory and brain activity changes during development.
Biological psychiatry 2011;70(3):222-9.
2011: Satu Wedenoja; Pia Höglund; Christer Holmberg; Siru Mäkelä; Elina Pekansaari; Juha Kere
Update on SLC26A3 mutations in congenital chloride diarrhea.
Human mutation 2011;32(7):715-22.
2011: Maria Sandbacka; Marita Lipsanen-Nyman; Minna Puhakka; Kristiina Aittomäki; Sara Bruce; Mervi Halttunen; Katariina Hannula-Jouppi; Juha Kere; Päivi Lahermo; Hannele Laivuori
Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia.
Fertility and sterility 2011;95(8):2703-6.
2011: Nicholas K Rorick; Akira Kinoshita; Jason L Weirather; Myriam Peyrard-Janvid; Renata L L Ferreira de Lima; Martine Dunnwald; Alan L Shanske; Danilo Moretti-Ferreira; Hannele Koillinen; Juha Kere; Maria A Mansilla; Jeffrey C Murray; Steve L Goudy; Brian C Schutte
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.
American journal of medical genetics. Part A 2011;155A(6):1314-21.
2011: Hong Jiao; Peter Arner; Suzanne L Dickson; Hubert Vidal; Niklas Mejhert; Corneliu Henegar; Magdalena Taube; Caroline Hansson; Anke Hinney; Pilar Galan; Chantal Simon; Angela Silveira; Anna Benrick; John-Olov Jansson; Anne Bouloumié; Dominique Langin; Martine Laville; Cyrille Debard; Tomas Axelsson; Mikael Rydén; Juha Kere; Karin Dahlman-Wright; Anders Hamsten; Karine Clement; Ingrid Dahlman
Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity.
The Journal of clinical endocrinology and metabolism 2011;96(6):E962-6.
2011: Elisabet Einarsdottir; Katri Kaukinen; Juha Kere; Ilma Korponay-Szabo; Lotta L E Koskinen; Kalle Kurppa; Markku Mäki; M Luisa Mearin; Alienke Monsuur; Chris Mulder; Ruben van't Slot; Cisca Wijmenga; Alexandra Zhernakova; Marianna R Bevova; Päivi Saavalainen
Multiple independent variants in 6q21-22 associated with susceptibility to celiac disease in the Dutch, Finnish and Hungarian populations.
European journal of human genetics : EJHG 2011;19(6):682-6.
2011: Liselotte Vesterlund; Virpi Töhönen; Outi Hovatta; Juha Kere
Co-localization of neural cell adhesion molecule and fibroblast growth factor receptor 2 in early embryo development.
The International journal of developmental biology 2011;55(3):313-9.
2011: Hong Jiao; Juha Kere; Oluf Pedersen; Ferdinand van't Hooft; Thorkild I A Sørensen; Peter Arner; Tomas Axelsson; David Brodin; Karine Clement; Sébastien Czernichow; Karin Dahlman-Wright; Beatrice Dubern; Anders Hamsten; Torben Hansen; Johannes Hebebrand; Johan Hoffstedt; Ingrid Dahlman
Genome wide association study identifies KCNMA1 contributing to human obesity.
BMC medical genomics 2011;4():51.
2011: Christina Orsmark Pietras; Ville Pulkkinen; Cilla Söderhäll; Lilli Sundman; Johanna Vendelin; Mikael Adner; Harri Alenius; Francesca Anedda; Sara Bruce; Mauro D'Amato; Juha Kere
The asthma candidate gene NPSR1 mediates isoform specific downstream signalling.
BMC pulmonary medicine 2011;11():39.
2011: Satu Massinen; Hans Matsson; Myriam Peyrard-Janvid; Peter Swoboda; Kristiina Tammimies; Isabel Tapia-Páez; Rune Toftgård; Jan Burghoorn; Eero Castrén; Vanina Dahlström-Heuser; Marie-Estelle Hokkanen; Kristian E Jeppsson; Juha Kuja-Panula; Juha Kere
Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons.
PloS one 2011;6(6):e20580.
2011: L Goumidi; Juha Kere; Jean-Charles Lambert; Hans Matsson; Philippe Amouyel; Karin Dahlman-Wright; Florence Pasquier; Isabel Tapia-Paez; Aline Meirhaeghe
Study of estrogen receptor-α and receptor-β gene polymorphisms on Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2011;26(3):431-9.
2011: Liselotte Vesterlund; Per Unneberg; Outi Hovatta; Hong Jiao; Juha Kere
The zebrafish transcriptome during early development.
BMC developmental biology 2011;11():30.
2011: Elina Salmela; Tuuli Lappalainen; Jianjun Liu; Pertti Sistonen; Peter M Andersen; Stefan Schreiber; Marja-Liisa Savontaus; Kamila Czene; Päivi Lahermo; Per Hall; Juha Kere
Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.
PloS one 2011;6(2):e16747.
2011: Hans Matsson; Kristiina Tammimies; Marco Zucchelli; Heidi Anthoni; Päivi Onkamo; Jaana Nopola-Hemmi; Heikki Lyytinen; Paavo H T Leppanen; Nina Neuhoff; Andreas Warnke; Gerd Schulte-Körne; Johannes Schumacher; Markus M Nöthen; Juha Kere; Myriam Peyrard-Janvid
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Behavior genetics 2011;41(1):134-40.
2011: Catarina Almqvist; Hans-Olov Adami; Paul W Franks; Leif Groop; Erik Ingelsson; Juha Kere; Lauren Lissner; Jan-Eric Litton; Markus J Maeurer; Karl Michaëlsson; Juni Palmgren; Göran Pershagen; Alexander Ploner; Patrick F Sullivan; Gunnel Tybring; Nancy L Pedersen
LifeGene--a large prospective population-based study of global relevance.
European journal of epidemiology 2011;26(1):67-77.
2010: Stina Söderqvist; Fiona McNab; Myriam Peyrard-Janvid; Hans Matsson; Keith Humphreys; Juha Kere; Torkel Klingberg
The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood.
Biological psychiatry 2010;68(12):1120-5.
2010: Sara Bruce; Katariina Hannula-Jouppi; Mari Puoskari; Ingegerd Fransson; Kalle O J Simola; Marita Lipsanen-Nyman; Juha Kere
Submicroscopic genomic alterations in Silver-Russell syndrome and Silver-Russell-like patients.
Journal of medical genetics 2010;47(12):816-22.
2010: Jonas Donner; Rita Haapakoski; Sini Ezer; Erik Melén; sami pirkola; Mònica Gratacòs; Marco Zucchelli; Francesca Anedda; Lovisa E Johansson; Cilla Söderhäll; Christina Orsmark-Pietras; Jaana Suvisaari; Rocío Martín-Santos; Marta Torrens; Kaisa Silander; Joseph D Terwilliger; Magnus Wickman; Göran Pershagen; Jouko Lönnqvist; Leena Peltonen; Xavier Estivill; Mauro D'Amato; Juha Kere; Harri Alenius; Iiris Hovatta
Assessment of the neuropeptide S system in anxiety disorders.
Biological psychiatry 2010;68(5):474-83.
2010: Emmanuelle Bouzigon; Paola Forabosco; Gerard H Koppelman; William O C M Cookson; Marie-Hélène Dizier; David L Duffy; David M Evans; Manuel A R Ferreira; Juha Kere; Tarja Laitinen; Giovanni Malerba; Deborah A Meyers; Miriam Moffatt; Nicholas G Martin; Mandy Y Ng; Pier Franco Pignatti; Mathias Wjst; Francine Kauffmann; Florence Demenais; Cathryn M Lewis
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy.
European journal of human genetics : EJHG 2010;18(6):700-6.
2010: Leena M Hiltunen; Hannele Laivuori; Anna Rautanen; Risto Kaaja; Juha Kere; Tom Krusius; Mikko Paunio; Vesa Rasi
Factor V Leiden as risk factor for unexplained stillbirth--a population-based nested case-control study.
Thrombosis research 2010;125(6):505-10.
2010: M Karppelin; T Siljander; Jaana Vuopio-Varkila; Juha Kere; Heini Huhtala; Risto Vuento; T Jussila; Jaana Syrjänen
Factors predisposing to acute and recurrent bacterial non-necrotizing cellulitis in hospitalized patients: a prospective case-control study.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases 2010;16(6):729-34.
2010: Juha Kere
Genetics of complex disorders.
Biochemical and biophysical research communications 2010;396(1):143-6.
2010: M Qu; H Jiao; Jian Zhao; Zhi-Ping Ren; Anja Smits; Juha Kere; Monica Nistér
Molecular genetic and epigenetic analysis of NCX2/SLC8A2 at 19q13.3 in human gliomas.
Neuropathology and applied neurobiology 2010;36(3):198-210.
2010: Ville Pulkkinen; Sara Bruce; Johanna Rintahaka; Ulla Hodgson; Tarja Laitinen; Harri Alenius; Vuokko L Kinnula; Marjukka Myllärniemi; Sampsa Matikainen; Juha Kere
ELMOD2, a candidate gene for idiopathic pulmonary fibrosis, regulates antiviral responses.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2010;24(4):1167-77.
2010: Tuuli Lappalainen; Elina Salmela; Peter M Andersen; Karin Dahlman-Wright; Pertti Sistonen; Marja-Liisa Savontaus; Stefan Schreiber; Päivi Lahermo; Juha Kere
Genomic landscape of positive natural selection in Northern European populations.
European journal of human genetics : EJHG 2010;18(4):471-8.
2010: S Panasevich; Cecilia M Lindgren; Juha Kere; Magnus Wickman; Göran Pershagen; Fredrik Nyberg; Erik Melén
Interaction between early maternal smoking and variants in TNF and GSTP1 in childhood wheezing.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2010;40(3):458-67.
2010: Tiina M Järvinen; Anna Hellquist; Sari Koskenmies; Elisabet Einarsdottir; Lotta L E Koskinen; Leila Jeskanen; Linda Berglind; Jaana Panelius; Taina Hasan; Annamari Ranki; Juha Kere; Ulpu Saarialho-Kere
Tyrosine kinase 2 and interferon regulatory factor 5 polymorphisms are associated with discoid and subacute cutaneous lupus erythematosus.
Experimental dermatology 2010;19(2):123-31.
2010: Tiina M Järvinen; Anna Hellquist; Sari Koskenmies; Elisabet Einarsdottir; Jaana Panelius; Taina Hasan; Heikki Julkunen; Leonid Padyukov; Marika Kvarnström; Marie Wahren-Herlenius; Filippa Nyberg; Mauro D'Amato; Juha Kere; Ulpu Saarialho-Kere
Polymorphisms of the ITGAM gene confer higher risk of discoid cutaneous than of systemic lupus erythematosus.
PloS one 2010;5(12):e14212.
2010: Juha Kere; Samuli Ripatti; Markus Perola
[Genetics of multifactorial diseases].
Duodecim; lääketieteellinen aikakauskirja 2010;126(19):2305-10.
2010: Jingmei Li; Keith Humphreys; Hatef Darabi; Gustaf Rosin; Ulf Hannelius; Tuomas Heikkinen; Kristiina Aittomäki; Carl Blomqvist; Paul Dp Pharoah; Alison M Dunning; Shahana Ahmed; Maartje J Hooning; Antoinette Hollestelle; Rogier A Oldenburg; Lars Alfredsson; Aarno Palotie; Leena Peltonen-Palotie; Astrid Irwanto; Hui Qi Low; Garrett Hk Teoh; Anbupalam Thalamuthu; Juha Kere; Mauro D'Amato; Douglas F Easton; Heli Nevanlinna; Jianjun Liu; Kamila Czene; Per Hall
A genome-wide association scan on estrogen receptor-negative breast cancer.
Breast cancer research : BCR 2010;12(6):R93.
2010: Michael Algovik; Katja Kivinen; Hanna Peterson; Magnus Westgren; Juha Kere
Genetic evidence of multiple loci in dystocia--difficult labour.
BMC medical genetics 2010;11():105.
2010: Outi Hovatta; Marisa Jaconi; Virpi Töhönen; Frédérique Béna; stefania gimelli; Alexis Bosman; Frida Holm; Stefan Wyder; Evgeny M Zdobnov; Olivier Irion; Peter W Andrews; Stylianos E Antonarakis; Marco Zucchelli; Juha Kere; Anis Feki
A teratocarcinoma-like human embryonic stem cell (hESC) line and four hESC lines reveal potentially oncogenic genomic changes.
PloS one 2010;5(4):e10263.
2010: Mauro D'Amato; Marco Zucchelli; Maria Seddighzadeh; Francesca Anedda; Staffan Lindblad; Juha Kere; Lars Alfredsson; Lars Klareskog; Leonid Padyukov
Analysis of neuropeptide S receptor gene (NPSR1) polymorphism in rheumatoid arthritis.
PloS one 2010;5(2):e9315.
2010: L Sundman; Ulpu Saarialho-Kere; Johanna Vendelin; Katri Lindfors; G Assadi; Katri Kaukinen; Mia Westerholm-Ormio; Erkki Savilahti; Markku Mäki; Harri Alenius; Mauro D'Amato; Ville Pulkkinen; Juha Kere; P Saavalainen
Neuropeptide S receptor 1 expression in the intestine and skin--putative role in peptide hormone secretion.
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2010;22(1):79-87, e30.
2009: Gary M Hunninghake; Michael H Cho; Yohannes Tesfaigzi; Manuel E Soto-Quiros; Lydiana Avila; Jessica Lasky-Su; Chris Stidley; Erik Melén; Cilla Söderhäll; Jenny Hallberg; Inger Kull; Juha Kere; Magnus Svartengren; Göran Pershagen; Magnus Wickman; Christoph Lange; Dawn L DeMeo; Craig Hersh; Barbara J Klanderman; Benjamin A Raby; David Sparrow; Steven D Shapiro; Edwin K Silverman; Augusto A Litonjua; Scott T Weiss; Juan C Celedón
MMP12, lung function, and COPD in high-risk populations.
The New England journal of medicine 2009;361(27):2599-608.
2009: L L E Koskinen; E Einarsdottir; Ilma Korponay-Szabo; K Kurppa; Katri Kaukinen; Pertti Sistonen; Zsuzsa Pocsai; G Széles; Róza Adány; Markku Mäki; Juha Kere; P Saavalainen
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.
Tissue antigens 2009;74(5):408-16.
2009: Marco Zucchelli; Leif Torkvist; Francesca Bresso; Jonas Halfvarson; Anna Hellquist; Francesca Anedda; Ghazaleh Assadi; Gunnar B Lindgren; Monika Svanfeldt; Martin Janson; Colin L Noble; Sven Pettersson; Maija Lappalainen; Paulina Paavola-Sakki; Leena Halme; Martti Färkkilä; Ulla Turunen; Jack Satsangi; Kimmo Kontula; Robert Löfberg; Juha Kere; Mauro D'Amato
PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.
Inflammatory bowel diseases 2009;15(10):1562-9.
2009: Anna Hellquist; Tiina M Järvinen; Sari Koskenmies; Marco Zucchelli; Christina Orsmark-Pietras; Linda Berglind; Jaana Panelius; Taina Hasan; Heikki Julkunen; Mauro D'Amato; Ulpu Saarialho-Kere; Juha Kere
Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus.
The Journal of rheumatology 2009;36(8):1631-8.
2009: Satu Massinen; Kristiina Tammimies; Isabel Tapia-Páez; Hans Matsson; Marie-Estelle Hokkanen; Ola Söderberg; Ulf Landegren; Eero Castrén; Jan-Ake Gustafsson; Eckardt Treuter; Juha Kere
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
Human molecular genetics 2009;18(15):2802-12.
2009: H Peterson; Hannele Laivuori; Erja Kerkelä; H Jiao; Liisa Hiltunen; S Heino; Inkeri Tiala; Sakari Knuutila; Vesa Rasi; Juha Kere; Katja Kivinen
ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.
Molecular human reproduction 2009;15(7):443-9.
2009: Marco Zucchelli; Leif Torkvist; Francesca Bresso; Jonas Halfvarson; Cilla Söderhäll; Young-Ae Lee; Robert Löfberg; Juha Kere; Mauro D'Amato
No association between the eczema genes COL29A1 and IL31 and inflammatory bowel disease.
Inflammatory bowel diseases 2009;15(7):961-2.
2009: Leena M Hiltunen; Hannele Laivuori; Anna Rautanen; Risto Kaaja; Juha Kere; Tom Krusius; Mikko Paunio; Vesa Rasi
Blood group AB and factor V Leiden as risk factors for pre-eclampsia: a population-based nested case-control study.
Thrombosis research 2009;124(2):167-73.
2009: Faten Dahdouh; Heidi Anthoni; Isabel Tapia-Páez; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Andreas Warnke; Helmut Remschmidt; Andreas Ziegler; Juha Kere; Bertram Müller-Myhsok; Markus M Nöthen; Johannes Schumacher; Marco Zucchelli
Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Psychiatric genetics 2009;19(2):59-63.
2009: Lotta L E Koskinen; Elisabet Einarsdottir; Emma Dukes; Graham A R Heap; Patrick Dubois; Ilma R Korponay-Szabo; Katri Kaukinen; Kalle Kurppa; Fabiana Ziberna; Serena Vatta; Tarcisio Not; Alessandro Ventura; Pertti Sistonen; Róza Adány; Zsuzsa Pocsai; György Széles; Markku Mäki; Juha Kere; Cisca Wijmenga; David A van Heel; Päivi Saavalainen
Association study of the IL18RAP locus in three European populations with coeliac disease.
Human molecular genetics 2009;18(6):1148-55.
2009: S Bruce; Fredrik Nyberg; Erik Melén; A James; V Pulkkinen; C Orsmark-Pietras; Anna Bergström; B Dahlén; Magnus Wickman; E von Mutius; G Doekes; R Lauener; J Riedler; W Eder; M van Hage; Göran Pershagen; A Scheynius; Juha Kere
The protective effect of farm animal exposure on childhood allergy is modified by NPSR1 polymorphisms.
Journal of medical genetics 2009;46(3):159-67.
2009: Sara Bruce; Katariina Hannula-Jouppi; Jari Peltonen; Juha Kere; Marita Lipsanen-Nyman
Clinically distinct epigenetic subgroups in Silver-Russell syndrome: the degree of H19 hypomethylation associates with phenotype severity and genital and skeletal anomalies.
The Journal of clinical endocrinology and metabolism 2009;94(2):579-87.
2009: Kati Kainu; Katja Kivinen; Marco Zucchelli; Sari Suomela; Juha Kere; Annica Inerot; Barbara S Baker; Anne V Powles; Lionel Fry; Lena Samuelsson; Ulpu Saarialho-Kere
Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families.
Experimental dermatology 2009;18(2):109-15.
2009: Huiling He; Rebecca Nagy; Sandya Liyanarachchi; Hong Jiao; Wei Li; Saul Suster; Juha Kere; Albert de La Chapelle
A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24.
Cancer research 2009;69(2):625-31.
2009: Anna Hellquist; Marco Zucchelli; Cecilia M Lindgren; Ulpu Saarialho-Kere; Tiina M Järvinen; Sari Koskenmies; Heikki Julkunen; Päivi Onkamo; Tiina Skoog; Jaana Panelius; Anne Räisänen-Sokolowski; Taina Hasan; Elisabeth Widen; Iva Gunnarson; Elisabet Svenungsson; Leonid Padyukov; Ghazaleh Assadi; Linda Berglind; Ville-Veikko Mäkelä; Katja Kivinen; Andrew Wong; Deborah S Cunningham Graham; Timothy J Vyse; Mauro D'Amato; Juha Kere
Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE).
PloS one 2009;4(12):e8037.
2009: Pu Zhang; Marco Zucchelli; Sara Bruce; Fredwell Hambiliki; Anneli Stavreus-Evers; Lev Levkov; Heli Skottman; Erja Kerkelä; Juha Kere; Outi Hovatta
Transcriptome profiling of human pre-implantation development.
PloS one 2009;4(11):e7844.
2009: Sari Suomela; Outi Elomaa; Tiina Skoog; Risto Ala-Aho; Leila Jeskanen; Jenita Pärssinen; Leena Latonen; Reidar Grénman; Juha Kere; Veli-Matti Kähäri; Ulpu Saarialho-Kere
CCHCR1 is up-regulated in skin cancer and associated with EGFR expression.
PloS one 2009;4(6):e6030.
2009: Elisabeth Ekelund; M Bradley; Stephan Weidinger; Dragan L Jovanovic; Catharina Johansson; Cecilia M Lindgren; Antonia Todorova; Thilo Jakob; Thomas Illig; Erika von Mutius; Charlotte Braun-Fahrländer; Gert Doekes; Josef Riedler; Annika Scheynius; Göran Pershagen; Ingrid Kockum; Juha Kere
Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populations.
Acta dermato-venereologica 2009;89(2):115-21.
2009: Elisabet Einarsdottir; Lotta L E Koskinen; Emma Dukes; Kati Kainu; Sari Suomela; Maija Lappalainen; Fabiana Ziberna; Ilma R Korponay-Szabo; Kalle Kurppa; Katri Kaukinen; Róza Adány; Zsuzsa Pocsai; György Széles; Martti Färkkilä; Ulla Turunen; Leena Halme; Paulina Paavola-Sakki; Tarcisio Not; Serena Vatta; Alessandro Ventura; Robert Löfberg; Leif Torkvist; Francesca Bresso; Jonas Halfvarson; Markku Mäki; Kimmo Kontula; Ulpu Saarialho-Kere; Juha Kere; Mauro D'Amato; Päivi Saavalainen
IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease.
BMC medical genetics 2009;10():8.
2009: T Lappalainen; Ulf Hannelius; Elina Salmela; U von Döbeln; Cecilia M Lindgren; Kirsi Huoponen; Marja-Liisa Savontaus; Juha Kere; Päivi Lahermo
Population structure in contemporary Sweden--a Y-chromosomal and mitochondrial DNA analysis.
Annals of human genetics 2009;73(1):61-73.
2008: Kerstin U Ludwig; Johannes Schumacher; Gerd Schulte-Körne; Inke R König; Andreas Warnke; Ellen Plume; Heidi Anthoni; Myriam Peyrard-Janvid; Haiying Meng; Andreas Ziegler; Helmut Remschmidt; Juha Kere; Jeffrey R Gruen; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Psychiatric genetics 2008;18(6):310-2.
2008: Hong Jiao; Beáta Tóth; Melinda Erdos; Ingegerd Fransson; Eva Rákóczi; Istvan Balogh; Zoltán Magyarics; Beáta Dérfalvi; Gabriella Csorba; Anna Szaflarska; Andre Megarbane; Carlo Akatcherian; Ghassan Dbaibo; Eva Rajnavölgyi; Lennart Hammarström; Juha Kere; Gérard Lefranc; László Maródi
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
Molecular immunology 2008;46(1):202-6.
2008: Satu Wedenoja; Timo Ormälä; Ulla B Berg; Stella F Edström Halling; Hannu Jalanko; Riitta Karikoski; Juha Kere; Christer Holmberg; Pia Höglund
The impact of sodium chloride and volume depletion in the chronic kidney disease of congenital chloride diarrhea.
Kidney international 2008;74(8):1085-93.
2008: Erik Melén; Fredrik Nyberg; Cecilia M Lindgren; Niklas Berglind; Marco Zucchelli; Emma Nordling; Jenny Hallberg; Magnus Svartengren; Ralf Morgenstern; Juha Kere; tom bellander; Magnus Wickman; Göran Pershagen
Interactions between glutathione S-transferase P1, tumor necrosis factor, and traffic-related air pollution for development of childhood allergic disease.
Environmental health perspectives 2008;116(8):1077-84.
2008: Isabel Tapia-Páez; Kristiina Tammimies; Satu Massinen; Ananda L Roy; Juha Kere
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2008;22(8):3001-9.
2008: Christina Orsmark-Pietras; Erik Melén; Johanna Vendelin; Sara Bruce; Annika Laitinen; Lauri A Laitinen; Roger Lauener; Josef Riedler; Erika von Mutius; Gert Doekes; Magnus Wickman; Marianne van Hage; Göran Pershagen; Annika Scheynius; Fredrik Nyberg; Juha Kere
Biological and genetic interaction between tenascin C and neuropeptide S receptor 1 in allergic diseases.
Human molecular genetics 2008;17(11):1673-82.
2008: H Jiao; Maria Kaaman; E Dungner; Juha Kere; Peter Arner; Ingrid Dahlman
Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis.
International journal of obesity (2005) 2008;32(5):816-25.
2008: M Pegelow; Myriam Peyrard-Janvid; Marco Zucchelli; Ingegerd Fransson; Ola Larson; Juha Kere; Catharina Larsson; Agneta Karsten
Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
European journal of orthodontics 2008;30(2):169-75.
2008: Inkeri Tiala; Janica Wakkinen; Sari Suomela; Pauli Puolakkainen; Raija Tammi; Sofi Forsberg; Ola Rollman; Kati Kainu; Björn Rozell; Juha Kere; Ulpu Saarialho-Kere; Outi Elomaa
The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice.
Human molecular genetics 2008;17(7):1043-51.
2008: L L E Koskinen; I R Korponay-Szabo; K Viiri; K Juuti-Uusitalo; K Kaukinen; Katri Lindfors; K Mustalahti; K Kurppa; R Adány; Z Pocsai; G Széles; E Einarsdottir; cisca wijmenga; Markku Mäki; Jukka Partanen; Juha Kere; P Saavalainen
Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association.
Journal of medical genetics 2008;45(4):222-7.
2008: Tuula Siljander; Matti Karppelin; Susanna Vähäkuopus; Jaana Syrjänen; Maija Toropainen; Juha Kere; Risto Vuento; Tapio Jussila; Jaana Vuopio-Varkila
Acute bacterial, nonnecrotizing cellulitis in Finland: microbiological findings.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2008;46(6):855-61.
2008: Sara Bruce; Katariina Hannula-Jouppi; Cecilia M Lindgren; Marita Lipsanen-Nyman; Juha Kere
Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR.
Clinical chemistry 2008;54(3):491-9.
2008: Elina Salmela; Tuuli Lappalainen; Ingegerd Fransson; Peter M Andersen; Karin Dahlman-Wright; Andreas Fiebig; Pertti Sistonen; Marja-Liisa Savontaus; Stefan Schreiber; Juha Kere; Päivi Lahermo
Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.
PloS one 2008;3(10):e3519.
2008: Ulf Hannelius; Elina Salmela; Tuuli Lappalainen; Gilles Guillot; Cecilia M Lindgren; Ulrika von Döbeln; Päivi Lahermo; Juha Kere
Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs.
BMC genetics 2008;9():54.
2008: Pu Zhang; Morag Dixon; Marco Zucchelli; Fredwell Hambiliki; Lev Levkov; Outi Hovatta; Juha Kere
Expression analysis of the NLRP gene family suggests a role in human preimplantation development.
PloS one 2008;3(7):e2755.
2007: Sharon Barone; Hassane Amlal; Minna Kujala; Jie Xu; Fiona E Karet; Ann Blanchard; Juha Kere; Manoocher Soleimani
Regulation of the basolateral chloride/base exchangers AE1 and SLC26A7 in the kidney collecting duct in potassium depletion.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007;22(12):3462-70.
2007: Mauro D'Amato; Sara Bruce; Francesca Bresso; Marco Zucchelli; Sini Ezer; Ville Pulkkinen; Cecilia Lindgren; Marco Astegiano; Mario Rizzetto; Paolo Gionchetti; Gabriele Riegler; Raffaello Sostegni; Marco Daperno; Sandra D'Alfonso; Patricia Momigliano-Richiardi; Leif Torkvist; Pauli Puolakkainen; Maija Lappalainen; Paulina Paavola-Sakki; Leena Halme; Martti Farkkila; Ulla Turunen; Kimmo Kontula; Robert Lofberg; Sven Pettersson; Juha Kere
Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease.
Gastroenterology 2007;133(3):808-17.
2007: Timo Otonkoski; Hong Jiao; Nina Kaminen-Ahola; Isabel Tapia-Paez; Mohammed S Ullah; Laura E Parton; Frans Schuit; Roel Quintens; Ilkka Sipilä; Ertan Mayatepek; Thomas Meissner; Andrew P Halestrap; Guy Rutter; Juha Kere
Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells.
American journal of human genetics 2007;81(3):467-74.
2007: Min Ae Lee-Kirsch; Maolian Gong; Dipanjan Chowdhury; Lydia Senenko; Kerstin Engel; Young-Ae Lee; Udesh de Silva; Suzanna L Bailey; Torsten Witte; Timothy J Vyse; Juha Kere; Christiane Pfeiffer; Scott Harvey; Andrew Wong; Sari Koskenmies; Oliver Hummel; Klaus Rohde; Reinhold E Schmidt; Anna F Dominiczak; Manfred Gahr; Thomas Hollis; Fred W Perrino; Judy Lieberman; Norbert Hübner
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.
Nature genetics 2007;39(9):1065-7.
2007: Ulf Hannelius; Loreana Gherman; Ville-Veikko Mäkelä; Astrid Lindstedt; Marco Zucchelli; Camilla Lagerberg; Gunnel Tybring; Juha Kere; Cecilia M Lindgren
Large-scale zygosity testing using single nucleotide polymorphisms.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2007;10(4):604-25.
2007: Miina Ollikainen; Ulf Hannelius; Cecilia M Lindgren; Wael M Abdel-Rahman; Juha Kere; Päivi Peltomäki
Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach.
Oncogene 2007;26(31):4541-9.
2007: Ingrid Dahlman; Andrea Dicker; Hong Jiao; Juha Kere; Lennart Blomqvist; Vanessa van Harmelen; Johan Hoffstedt; Knut Borch-Johnsen; Torben Jorgensen; Torben Hansen; Oluf Pedersen; Markku Laakso; Peter Arner
A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis.
American journal of human genetics 2007;80(6):1115-24.
2007: Inkeri Tiala; Sari Suomela; Jari Huuhtanen; Janica Wakkinen; Maarit Hölttä-Vuori; Kati Kainu; Sirpa Ranta; Ursula Turpeinen; Esa Hämäläinen; Hong Jiao; Seija-Liisa Karvonen; Elina Ikonen; Juha Kere; Ulpu Saarialho-Kere; Outi Elomaa
The CCHCR1 (HCR) gene is relevant for skin steroidogenesis and downregulated in cultured psoriatic keratinocytes.
Journal of molecular medicine (Berlin, Germany) 2007;85(6):589-601.
2007: Anna Hellquist; Marco Zucchelli; Katja Kivinen; Ulpu Saarialho-Kere; Sari Koskenmies; Elisabeth Widen; Heikki Julkunen; Andrew Wong; Marja-Liisa Karjalainen-Lindsberg; Tiina Skoog; Johanna Vendelin; Deborah S Cunninghame-Graham; Timothy J Vyse; Juha Kere; Cecilia M Lindgren
The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus.
Journal of medical genetics 2007;44(5):314-21.
2007: Katri Pylkäs; Johanna Tommiska; Kirsi Syrjäkoski; Juha Kere; Magtouf Gatei; Nicola Waddell; Minna Allinen; Sanna-Maria Karppinen; Katrin Rapakko; Helena Kääriäinen; Kristiina Aittomäki; Carl Blomqvist; Aki Mustonen; Kaija Holli; Kum Kum Khanna; Olli Kallioniemi; Heli Nevanlinna; Robert Winqvist
Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer.
Carcinogenesis 2007;28(5):1040-5.
2007: Minna Kujala; Satu Hihnala; Jukka Tienari; Kari Kaunisto; Johanna Hästbacka; Christer Holmberg; Juha Kere; Pia Höglund
Expression of ion transport-associated proteins in human efferent and epididymal ducts.
Reproduction (Cambridge, England) 2007;133(4):775-84.
2007: Katja Kivinen; Hanna Peterson; Liisa Hiltunen; Hannele Laivuori; Sanna Heino; Inkeri Tiala; Sakari Knuutila; Vesa Rasi; Juha Kere
Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample.
European journal of human genetics : EJHG 2007;15(4):494-7.
2007: Heidi Anthoni; Marco Zucchelli; Hans Matsson; Bertram Müller-Myhsok; Ingegerd Fransson; Johannes Schumacher; Satu Massinen; Päivi Onkamo; Andreas Warnke; Heide Griesemann; Per Hoffmann; Jaana Nopola-Hemmi; Heikki Lyytinen; Gerd Schulte-Körne; Juha Kere; Markus M Nöthen; Myriam Peyrard-Janvid
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Human molecular genetics 2007;16(6):667-77.
2007: Hannele Erkko; Bing Xia; Jenni Nikkilä; Johanna Schleutker; Kirsi Syrjäkoski; Arto Mannermaa; Anne Kallioniemi; Katri Pylkäs; Sanna-Maria Karppinen; Katrin Rapakko; alexander miron; Qing Sheng; Guilan Li; Henna Mattila; Daphne W Bell; Daniel A Haber; Mervi Grip; Mervi Reiman; Arja Jukkola-Vuorinen; Aki Mustonen; Juha Kere; Lauri A Aaltonen; Veli-Matti Kosma; Vesa Kataja; Ylermi Soini; Ronny Drapkin; David M Livingston; Robert Winqvist
A recurrent mutation in PALB2 in Finnish cancer families.
Nature 2007;446(7133):316-9.
2007: Pu Zhang; Erja Kerkelä; Heli Skottman; Lev Levkov; Katja Kivinen; Riitta Lahesmaa; Outi Hovatta; Juha Kere
Distinct sets of developmentally regulated genes that are expressed by human oocytes and human embryonic stem cells.
Fertility and sterility 2007;87(3):677-90.
2007: Erja Kerkelä; Heli Skottman; Barbro Friden; Kerstin Bjuresten; Juha Kere; Outi Hovatta
Exclusion of coding-region mutations in luteinizing hormone and follicle-stimulating hormone receptor genes as the cause of ovarian hyperstimulation syndrome.
Fertility and sterility 2007;87(3):603-6.
2007: Shasha Lu; Chen Zhao; Hong Jiao; Juha Kere; Xin Tang; Feng Zhao; Xiumei Zhang; Kanxing Zhao; Catharina Larsson
Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations.
Molecular vision 2007;13():1154-60.
2007: Juha Kere
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Duodecim; lääketieteellinen aikakauskirja 2007;123(8):864-6.
2007: Christina Orsmark; Tiina Skoog; Leila Jeskanen; Juha Kere; Ulpu Saarialho-Kere
Expression of allograft inflammatory factor-1 in inflammatory skin disorders.
Acta dermato-venereologica 2007;87(3):223-7.
2007: Sari Suomela; Kati Kainu; Päivi Onkamo; Inkeri Tiala; Johan Himberg; Lotta Koskinen; Erna Snellman; Seija-Liisa Karvonen; Juha T Karvonen; Tutta Uurasmaa; Timo Reunala; Kristiina Kivikäs; Christer T Jansén; Päivi Holopainen; Outi Elomaa; Juha Kere; Ulpu Saarialho-Kere
Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.
Acta dermato-venereologica 2007;87(2):127-34.
2007: Liisa Hiltunen; Anna Rautanen; Vesa Rasi; Risto Kaaja; Juha Kere; Tom Krusius; Elina Vahtera; Mikko Paunio
An unfavorable combination of Factor V Leiden with age, weight, and blood group causes high risk of pregnancy-associated venous thrombosis: a population-based nested case-control study.
Thrombosis research 2007;119(4):423-32.
2006: Ingrid Dahlman; Maria Nilsson; Hong Jiao; Johan Hoffstedt; Cecilia M Lindgren; Keith Humphreys; Juha Kere; Jan-�ke GUSTAFSSON; Peter Arner; Karin Dahlman-Wright
Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity.
Pharmacogenetics and genomics 2006;16(12):881-9.
2006: Erik Melén; S Umerkajeff; Fredrik Nyberg; Marco Zucchelli; Astrid Lindstedt; Harriet Gullstén; Magnus Wickman; Göran Pershagen; Juha Kere
Interaction between variants in the interleukin-4 receptor alpha and interleukin-9 receptor genes in childhood wheezing: evidence from a birth cohort study.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2006;36(11):1391-8.
2006: Lars Feuk; Aino Kalervo; Marita Lipsanen-Nyman; Jennifer Skaug; Kazuhiko Nakabayashi; Brenda Finucane; Danielle Hartung; Micheil Innes; Batsheva Kerem; Malgorzata J M Nowaczyk; Joseph Rivlin; Wendy Roberts; Lili Senman; Anne Summers; Peter Szatmari; Virginia Wong; John B Vincent; Susan Zeesman; Lucy Osborne; Janis Oram Cardy; Juha Kere; Stephen W Scherer; Katariina Hannula-Jouppi
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
American journal of human genetics 2006;79(5):965-72.
2006: Anna Rautanen; Johan G Eriksson; Juha Kere; Sture Andersson; Clive Osmond; Pentti J Tienari; Heikki Sairanen; David J P Barker; David I W Phillips; Tom Forsén; Eero Kajantie
Associations of body size at birth with late-life cortisol concentrations and glucose tolerance are modified by haplotypes of the glucocorticoid receptor gene.
The Journal of clinical endocrinology and metabolism 2006;91(11):4544-51.
2006: Sanna-Maria Karppinen; Rosa B Barkardottir; K Backenhorn; T Sydenham; Kirsi Syrjäkoski; Johanna Schleutker; Tarja Ikonen; Katri Pylkäs; Katrin Rapakko; Hannele Erkko; Gudrun Johannesdottir; Anne-Marie Gerdes; Mads Thomassen; Bjarni A Agnarsson; M Grip; Anne Kallioniemi; Juha Kere; Lauri A Aaltonen; Adalgeir Arason; P Møller; Torben A Kruse; Ake Borg; Robert Winqvist
Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies.
Journal of medical genetics 2006;43(11):856-62.
2006: Johanna Vendelin; Sara Bruce; Päivi Holopainen; Ville Pulkkinen; Paula Rytilä; Asta Pirskanen; Marko Rehn; Tarja Laitinen; Lauri A Laitinen; Tari Haahtela; Ulpu Saarialho-Kere; Annika Laitinen; Juha Kere
Downstream target genes of the neuropeptide S-NPSR1 pathway.
Human molecular genetics 2006;15(19):2923-35.
2006: Elias Zintzaras; GEORGIOS KITSIOS; Gavan A Harrison; Hannele Laivuori; Katja Kivinen; Juha Kere; Ioannis E Messinis; Ioannis Stefanidis; John Ioannidis
Heterogeneity-based genome search meta-analysis for preeclampsia.
Human genetics 2006;120(3):360-70.
2006: Päivi Lahermo; Ulrika Liljedahl; Grethe Alnaes; Tomas Axelsson; Anthony J Brookes; Pekka Ellonen; Per-Henrik Groop; Christer Halldén; Dan Holmberg; Kristina Holmberg; Mauri Keinänen; Katrin Kepp; Juha Kere; Päivi Kiviluoma; Vessela N Kristensen; Cecilia Lindgren; Jacob Odeberg; Pia Osterman; Maija Parkkonen; Janna Saarela; Maria Sterner; Linda Strömqvist; Ulvi Talas; Maija Wessman; Aarno Palotie; Ann-Christine Syvänen
A quality assessment survey of SNP genotyping laboratories.
Human mutation 2006;27(7):711-4.
2006: Ulla Hodgson; Ville Pulkkinen; Morag Dixon; Myriam Peyrard-Janvid; Marko Rehn; Päivi Lahermo; Vesa Ollikainen; Kaisa Salmenkivi; Vuokko Kinnula; Juha Kere; Pentti Tukiainen; Tarja Laitinen
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.
American journal of human genetics 2006;79(1):149-54.
2006: Elina Salmela; O Taskinen; Jouni K Seppänen; Pertti Sistonen; M J Daly; Päivi Lahermo; Marja-Liisa Savontaus; Juha Kere
Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.
Journal of medical genetics 2006;43(7):590-7.
2006: E Ekelund; A Saaf; Maria Tengvall-Linder; E Melen; Jenny Link; J Barker; Nick J Reynolds; Simon J Meggitt; Juha Kere; Carl-Fredrik Wahlgren; G Pershagen; M Wickman; M Nordenskjold; Ingrid Kockum; M Bradley
Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis.
American journal of human genetics 2006;78(6):1060-5.
2006: Philip De Jager; R Graham; Lisa Farwell; Stephen Sawcer; A Richardson; timothy wayne behrens; Alastair Compston; David A Hafler; Juha Kere; Timothy J Vyse; John D Rioux
The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus.
Genes and immunity 2006;7(4):327-34.
2006: Ville Pulkkinen; Marja-Leena Majuri; Guoying Wang; Päivi Holopainen; Yasushi Obase; Johanna Vendelin; Henrik Wolff; Paula Rytilä; Lauri A Laitinen; Tari Haahtela; Tarja Laitinen; Harri Alenius; Juha Kere; Marko Rehn
Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses.
Human molecular genetics 2006;15(10):1667-79.
2006: Karin Ekström Smedby; Cecilia M Lindgren; Henrik Hjalgrim; Keith Humphreys; Claudia Schöllkopf; Ellen T Chang; Göran Roos; lars peter ryder; Kerstin I Falk; Juni Palmgren; Juha Kere; Mads Melbye; Bengt Glimelius; Hans-Olov Adami
Variation in DNA repair genes ERCC2, XRCC1, and XRCC3 and risk of follicular lymphoma.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006;15(2):258-65.
2006: Satu Hihnala; Minna Kujala; J Toppari; Juha Kere; Christer Holmberg; Pia Höglund
Expression of SLC26A3, CFTR and NHE3 in the human male reproductive tract: role in male subfertility caused by congenital chloride diarrhoea.
Molecular human reproduction 2006;12(2):107-11.
2006: A Sillén; Charlotte Forsell; Lena Lilius; Karin Axelman; Behnosh F Björk; Päivi Onkamo; Juha Kere; Bengt Winblad; Caroline Graff
Genome scan on Swedish Alzheimer's disease families.
Molecular psychiatry 2006;11(2):182-6.
2006: Juha Kere
Overview of the SLC26 family and associated diseases.
Novartis Foundation symposium 2006;273():2-11; discussion 11-8, 261-4.
2006: Ville Pulkkinen; Ritva Haataja; Ulf Hannelius; Otto Helve; Olli M Pitkänen; Riitta Karikoski; Marko Rehn; Riitta Marttila; Cecilia M Lindgren; Johanna Hästbacka; Sture Andersson; Juha Kere; Mikko Hallman; Tarja Laitinen
G protein-coupled receptor for asthma susceptibility associates with respiratory distress syndrome.
Annals of medicine 2006;38(5):357-66.
2006: Johannes Schumacher; Heidi Anthoni; Faten Dahdouh; Inke R König; Axel M Hillmer; Nadine Kluck; Malou Manthey; Ellen Plume; Andreas Warnke; Helmut Remschmidt; Jutta Hülsmann; Sven Cichon; Cecilia M Lindgren; Peter Propping; Marco Zucchelli; Andreas Ziegler; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Markus M Nöthen; Juha Kere
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
American journal of human genetics 2006;78(1):52-62.
2005: Myriam Peyrard-Janvid; Marie Pegelow; Hannele Koillinen; Catharina Larsson; Ingegerd Fransson; Jorma Rautio; Jyri Hukki; Ola Larson; Agneta Karsten; Juha Kere
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
European journal of human genetics : EJHG 2005;13(12):1261-7.
2005: Anna Rautanen; Marco Zucchelli; Siru Mäkelä; Juha Kere
Gene mapping with pooled samples on three genotyping platforms.
Molecular and cellular probes 2005;19(6):408-16.
2005: Satu Kinnunen; Sandra Bonache; Teresa Casals; Sanni Monto; Erkki Savilahti; Juha Kere; Irma Järvelä
Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2005;4(4):233-7.
2005: S Bruce; R Leinonen; Cecilia M Lindgren; Katja Kivinen; Karin Dahlman-Wright; Marita Lipsanen-Nyman; Katariina Hannula-Jouppi; Juha Kere
Global analysis of uniparental disomy using high density genotyping arrays.
Journal of medical genetics 2005;42(11):847-51.
2005: Hong Jiao; Ingrid Dahlman; Per Eriksson; Juha Kere; Peter Arner
A common beta2-adrenoceptor gene haplotype protects against obesity in Swedish women.
Obesity research 2005;13(10):1645-50.
2005: Katariina Hannula-Jouppi; Nina Kaminen-Ahola; Mikko Taipale; Ranja Eklund; Jaana Nopola-Hemmi; Helena Kääriäinen; Juha Kere
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.
PLoS genetics 2005;1(4):e50.
2005: Ulf Hannelius; Cecilia M Lindgren; Erik Melén; A Malmberg; U von Dobeln; Juha Kere
Phenylketonuria screening registry as a resource for population genetic studies.
Journal of medical genetics 2005;42(10):e60.
2005: Ingrid Dahlman; Maria Kaaman; Hong Jiao; Juha Kere; Markku Laakso; Peter Arner
The CIDEA gene V115F polymorphism is associated with obesity in Swedish subjects.
Diabetes 2005;54(10):3032-4.
2005: Johanna Vendelin; Ville Pulkkinen; Marko Rehn; Asta Pirskanen; Anne Räisänen-Sokolowski; Annika Laitinen; Lauri A Laitinen; Juha Kere; Tarja Laitinen
Characterization of GPRA, a novel G protein-coupled receptor related to asthma.
American journal of respiratory cell and molecular biology 2005;33(3):262-70.
2005: Juha Kere
Mapping and identifying genes for asthma and psoriasis.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2005;360(1460):1551-61.
2005: Colin Veal; Nick J Reynolds; Simon J Meggitt; Michael H Allen; Cecilia M Lindgren; Juha Kere; Richard C Trembath; J N W N Barker
Absence of association between asthma and high serum immunoglobulin E associated GPRA haplotypes and adult atopic dermatitis.
The Journal of investigative dermatology 2005;125(2):399-401.
2005: Hui Wu; Rita M Cantor; Deborah S Cunninghame Graham; Cecilia M Lingren; Lisa Farwell; Philip L De Jager; Nunzio Bottini; Jennifer M Grossman; Daniel J Wallace; Bevra H Hahn; Heikki Julkunen; Lee A Hebert; Brad H Rovin; Daniel J Birmingham; John D Rioux; C Yung Yu; Juha Kere; Timothy J Vyse; Betty P Tsao
Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease.
Arthritis and rheumatism 2005;52(8):2396-402.
2005: Marja Sankelo; Julia A Flanagan; Rajiv Machado; Rachel Harrison; Nung Rudarakanchana; Nicholas W Morrell; Morag Dixon; Maija Halme; Hannu Puolijoki; Juha Kere; Outi Elomaa; Markku Kupari; Anne Räisänen-Sokolowski; Richard C Trembath; Tarja Laitinen
BMPR2 mutations have short lifetime expectancy in primary pulmonary hypertension.
Human mutation 2005;26(2):119-24.
2005: Johan Holmkvist; Peter Almgren; Hemang Parikh; Marco Zucchelli; Juha Kere; Leif Groop; Cecilia M Lindgren
Haplotype construction of the FRDA gene and evaluation of its role in type II diabetes.
European journal of human genetics : EJHG 2005;13(7):849-55.
2005: Erik Melén; Sara Bruce; Gert Doekes; Michael Kabesch; Tarja Laitinen; Roger Lauener; Cecilia M Lindgren; Josef Riedler; Annika Scheynius; Marianne Van Hage-Hamsten; Juha Kere; Göran Pershagen; Magnus Wickman; Fredrik Nyberg
Haplotypes of G protein-coupled receptor 154 are associated with childhood allergy and asthma.
American journal of respiratory and critical care medicine 2005;171(10):1089-95.
2005: Maria Swanberg; Olle Lidman; Leonid Padyukov; Per Eriksson; Eva Akesson; Maja Jagodic; Anna Lobell; Mohsen Khademi; Ola Börjesson; Cecilia M Lindgren; Pia Lundman; Anthony J Brookes; Juha Kere; Holger Luthman; Lars Alfredsson; Jan Hillert; Lars Klareskog; Anders Hamsten; Fredrik Piehl; Tomas Olsson
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction.
Nature genetics 2005;37(5):486-94.
2005: Marina N Chernova; Lianwei Jiang; David J Friedman; Rachel B Darman; Hannes Lohi; Juha Kere; David H Vandorpe; Seth L Alper
Functional comparison of mouse slc26a6 anion exchanger with human SLC26A6 polypeptide variants: differences in anion selectivity, regulation, and electrogenicity.
The Journal of biological chemistry 2005;280(9):8564-80.
2005: Snaevar Sigurdsson; Gunnel Nordmark; Harald HH Goring; Katarina Lindroos; Ann-Christin Wiman; Gunnar Sturfelt; Andreas Jönsen; Solbritt Rantapää-Dahlqvist; Bozena Möller; Juha Kere; Sari Koskenmies; Elisabeth Widén; Maija-Leena Eloranta; Heikki Julkunen; Helga Kristjansdottir; Kristjan Steinsson; Gunnar V Alm; Lars Rönnblom; Ann-Christine Syvänen
Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus.
American journal of human genetics 2005;76(3):528-37.
2005: Hannele Koillinen; Päivi Lahermo; Jorma Rautio; Jyri Hukki; Myriam Peyrard-Janvid; Juha Kere
A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.
Journal of medical genetics 2005;42(2):177-84.
2005: Siru Mäkelä; R Eklund; Jaana Lähdetie; Marja L Mikkola; Outi Hovatta; Juha Kere
Mutational analysis of the human SLC26A8 gene: exclusion as a candidate for male infertility due to primary spermatogenic failure.
Molecular human reproduction 2005;11(2):129-32.
2005: Juha Kere
Mapping genes for asthma and psoriasis.
Novartis Foundation symposium 2005;267():46-52; discussion 52-6.
2005: Minna Kujala; Jukka Tienari; Hannes Lohi; Outi Elomaa; Hannu Sariola; Eero Lehtonen; Juha Kere
SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney.
Nephron. Experimental nephrology 2005;101(2):e50-8.
2005: Maritta Pykäläinen; Riikka Kinos; Sanna Valkonen; Pia Rydman; Maritta Kilpeläinen; Lauri A Laitinen; Jussi Karjalainen; Markku Nieminen; Mikko Hurme; Juha Kere; Tarja Laitinen; Riitta Lahesmaa
Association analysis of common variants of STAT6, GATA3, and STAT4 to asthma and high serum IgE phenotypes.
The Journal of allergy and clinical immunology 2005;115(1):80-7.
2005: Tero Ylisaukko-Oja; Myriam Peyrard-Janvid; Cecilia M Lindgren; Karola Rehnström; Raija Vanhala; Leena Peltonen; Irma Järvelä; Juha Kere
Family-based association study of DYX1C1 variants in autism.
European journal of human genetics : EJHG 2005;13(1):127-30.
2004: Erik Melén; Harriet Gullstén; Marco Zucchelli; Astrid Lindstedt; Fredrik Nyberg; Magnus Wickman; Göran Pershagen; Juha Kere
Sex specific protective effects of interleukin-9 receptor haplotypes on childhood wheezing and sensitisation.
Journal of medical genetics 2004;41(12):e123.
2004: Juha Kere; Tarja Laitinen
Positionally cloned susceptibility genes in allergy and asthma.
Current opinion in immunology 2004;16(6):689-94.
2004: Ingrid Dahlman; P Eriksson; Maria Kaaman; H Jiao; Cecilia M Lindgren; Juha Kere; Peter Arner
alpha2-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action.
Diabetologia 2004;47(11):1974-9.
2004: Eero Kajantie; Anna Rautanen; Juha Kere; Sture Andersson; Hilkka Ylihärsilä; Clive Osmond; David J P Barker; Tom Forsén; Johan Eriksson
The effects of the ACE gene insertion/deletion polymorphism on glucose tolerance and insulin secretion in elderly people are modified by birth weight.
The Journal of clinical endocrinology and metabolism 2004;89(11):5738-41.
2004: Sharon Barone; Hassane Amlal; Jie Xu; Minna Kujala; Juha Kere; Snezana Petrovic; Manoocher Soleimani
Differential regulation of basolateral Cl-/HCO3- exchangers SLC26A7 and AE1 in kidney outer medullary collecting duct.
Journal of the American Society of Nephrology : JASN 2004;15(8):2002-11.
2004: Outi Elomaa; Inkeri Majuri; Sari Suomela; Kati Asumalahti; Hong Jiao; Zahra Mirzaei; Bjorn Rozell; Karin Dahlman-Wright; Johanna Pispa; Juha Kere; Ulpu Saarialho-Kere
Transgenic mouse models support HCR as an effector gene in the PSORS1 locus.
Human molecular genetics 2004;13(15):1551-61.
2004: Emmi K Ylikoski; Riikka Kinos; N Sirkkanen; Maritta Pykäläinen; Johannes Savolainen; L A Laitinen; Juha Kere; T Laitinen; Riitta Lahesmaa
Association study of 15 novel single-nucleotide polymorphisms of the T-bet locus among Finnish asthma families.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2004;34(7):1049-55.
2004: Erik Melén; Juha Kere; Göran Pershagen; Magnus Svartengren; Magnus Wickman
Influence of male sex and parental allergic disease on childhood wheezing: role of interactions.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2004;34(6):839-44.
2004: Sari Koskenmies; Elisabeth Widén; Päivi Onkamo; Petteri Sevón; Heikki Julkunen; Juha Kere
Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus.
European journal of human genetics : EJHG 2004;12(6):489-94.
2004: Tarja Laitinen; Anne Polvi; Pia Rydman; Johanna Vendelin; Ville Pulkkinen; Paula Salmikangas; Siru Mäkelä; Marko Rehn; Asta Pirskanen; Anna Rautanen; Marco Zucchelli; Harriet Gullstén; Marina Leino; Harri Alenius; Tuula Petäys; Tari Haahtela; Annika Laitinen; Catherine Laprise; Thomas J Hudson; Lauri A Laitinen; Juha Kere
Characterization of a common susceptibility locus for asthma-related traits.
Science (New York, N.Y.) 2004;304(5668):300-4.
2004: Myriam Peyrard-Janvid; Heidi Anthoni; Päivi Onkamo; Päivi Lahermo; Marco Zucchelli; Nina Kaminen; Katariina Hannula-Jouppi; Jaana Nopola-Hemmi; Arja Voutilainen; Heikki Lyytinen; Juha Kere
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Human genetics 2004;114(5):510-6.
2004: Vuokko L Kinnula; Siri T Lehtonen; Pirjo Koistinen; Sakari Kakko; Markku Savolainen; Juha Kere; Vesa Ollikainen; Tarja Laitinen
Two functional variants of the superoxide dismutase genes in Finnish families with asthma.
Thorax 2004;59(2):116-9.
2004: Sari Koskenmies; Outi Vaarala; Elisabeth Widen; Juha Kere; Timo Palosuo; Heikki Julkunen
The association of antibodies to cardiolipin, beta 2-glycoprotein I, prothrombin, and oxidized low-density lipoprotein with thrombosis in 292 patients with familial and sporadic systemic lupus erythematosus.
Scandinavian journal of rheumatology 2004;33(4):246-52.
2004: Sari Koskenmies; Päivi Lahermo; Heikki Julkunen; Vesa Ollikainen; Juha Kere; Elisabeth Widén
Linkage mapping of systemic lupus erythematosus (SLE) in Finnish families multiply affected by SLE.
Journal of medical genetics 2004;41(1):e2-5.
2004: Snezana Petrovic; Sharon Barone; Jie Xu; Laura Conforti; Liyun Ma; Minna Kujala; Juha Kere; Manoocher Soleimani
SLC26A7: a basolateral Cl-/HCO3- exchanger specific to intercalated cells of the outer medullary collecting duct.
American journal of physiology. Renal physiology 2004;286(1):F161-9.
2003: Sari Suomela; Outi Elomaa; Kati Asumalahti; Arja-Leena Kariniemi; Seija-Liisa Karvonen; Juha Peltonen; Juha Kere; Ulpu Saarialho-Kere
HCR, a candidate gene for psoriasis, is expressed differently in psoriasis and other hyperproliferative skin disorders and is downregulated by interferon-gamma in keratinocytes.
The Journal of investigative dermatology 2003;121(6):1360-4.
2003: Kati Asumalahti; Tarja Laitinen; Päivi Lahermo; Sari Suomela; Raija Itkonen-Vatjus; Christer Jansen; Juha T Karvonen; Seija-Liisa Karvonen; Timo Reunala; Erna Snellman; Tutta Uurasmaa; Ulpu Saarialho-Kere; Juha Kere
Psoriasis susceptibility locus on 18p revealed by genome scan in Finnish families not associated with PSORS1.
The Journal of investigative dermatology 2003;121(4):735-40.
2003: Mikko Taipale; Nina Kaminen; Jaana Nopola-Hemmi; Tuomas Haltia; Birgitta Myllyluoma; Heikki Lyytinen; Kurt Muller; Minna Kaaranen; Perttu J Lindsberg; Katariina Hannula-Jouppi; Juha Kere
A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(20):11553-8.
2003: Hannele Koillinen; Vesa Ollikainen; Jorma Rautio; Jyri Hukki; Juha Kere
Linkage and linkage disequilibrium searched for between non-syndromic cleft palate and four candidate loci.
Journal of medical genetics 2003;40(6):464-8.
2003: Snezana Petrovic; Xie Ju; Sharon Barone; Ursula Seidler; Seth L Alper; Hannes Lohi; Juha Kere; Manoocher Soleimani
Identification of a basolateral Cl-/HCO3- exchanger specific to gastric parietal cells.
American journal of physiology. Gastrointestinal and liver physiology 2003;284(6):G1093-103.
2003: Nina Kaminen; Katariina Hannula-Jouppi; Marjo Kestilä; Päivi Lahermo; K Muller; M Kaaranen; Birgitta Myllyluoma; Arja Voutilainen; Heikki Lyytinen; Jaana Nopola-Hemmi; Juha Kere
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.
Journal of medical genetics 2003;40(5):340-5.
2003: Kati Asumalahti; Mahreen Ameen; Sari Suomela; Eva Hagforsen; Gerd Michaëlsson; Julie Evans; Margo Munro; Colin Veal; Michael Allen; Joyce Leman; A David Burden; Brian Kirby; Maureen Connolly; Christopher E M Griffiths; Richard C Trembath; Juha Kere; Ulpu Saarialho-Kere; J N W N Barker
Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis.
The Journal of investigative dermatology 2003;120(4):627-32.
2003: Miia Melkoniemi; Hannele Koillinen; Minna Männikkö; Matthew L Warman; Tero Pihlajamaa; Helena Kääriäinen; Jorma Rautio; Jyri Hukki; Joseph A Stofko; George J Cisneros; Deborah Krakow; Daniel H Cohn; Juha Kere; Leena Ala-Kokko
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
European journal of human genetics : EJHG 2003;11(3):265-70.
2003: Hannes Lohi; Georg Lamprecht; Daniel Markovich; Anders Heil; Minna Kujala; Ursula Seidler; Juha Kere
Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains.
American journal of physiology. Cell physiology 2003;284(3):C769-79.
2003: Kati Asumalahti; Ulpu Saarialho-Kere; Juha Kere
[The pathogenesis of psoriasis--investigating the genetics of a multifactorial disease].
Duodecim; lääketieteellinen aikakauskirja 2003;119(16):1517-22.
2003: Timo Otonkoski; Nina Kaminen; Jarkko Ustinov; Risto Lapatto; Thomas Meissner; Ertan Mayatepek; Juha Kere; Ilkka Sipilä
Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release.
Diabetes 2003;52(1):199-204.
2003: Hannele Laivuori; Päivi Lahermo; Vesa Ollikainen; Elisabeth Widen; Leena Häivä-Mällinen; Helena Sundström; Tarja Laitinen; Risto Kaaja; Olavi Ylikorkala; Juha Kere
Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.
American journal of human genetics 2003;72(1):168-77.
2002: Ying Zhu; Jaakko Hollmén; Riikka Räty; Yan Aalto; Balint Nagy; Erkki Elonen; Juha Kere; Heikki Mannila; Kaarle Franssila; Sakari Knuutila
Investigatory and analytical approaches to differential gene expression profiling in mantle cell lymphoma.
British journal of haematology 2002;119(4):905-15.
2002: Siru Mäkelä; Juha Kere; Christer Holmberg; Pia Höglund
SLC26A3 mutations in congenital chloride diarrhea.
Human mutation 2002;20(6):425-38.
2002: Katja Ahokas; Jouko Lohi; Hannes Lohi; Outi Elomaa; Marja-Liisa Karjalainen-Lindsberg; Juha Kere; Ulpu Saarialho-Kere
Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancer.
Gene 2002;301(1-2):31-41.
2002: Päivi Onkamo; Vesa Ollikainen; Petteri Sevon; Hannu Toivonen; Heikki Mannila; Juha Kere
Association analysis for quantitative traits by data mining: QHPM.
Annals of human genetics 2002;66(Pt 5-6):419-29.
2002: Anne Polvi; Tuomas Polvi; Petteri Sevon; Tuula Petäys; Tari Haahtela; Lauri A Laitinen; Juha Kere; Tarja Laitinen
Physical map of an asthma susceptibility locus in 7p15-p14 and an association study of TCRG.
European journal of human genetics : EJHG 2002;10(10):658-65.
2002: Jaana Nopola-Hemmi; Birgitta Myllyluoma; Arja Voutilainen; Seija Leinonen; Juha Kere; Timo Ahonen
Familial dyslexia: neurocognitive and genetic correlation in a large Finnish family.
Developmental medicine and child neurology 2002;44(9):580-6.
2002: Nina Woolley; Päivi Holopainen; Vesa Ollikainen; Kirsi Mustalahti; Markku Mäki; Juha Kere; Jukka Partanen
A new locus for coeliac disease mapped to chromosome 15 in a population isolate.
Human genetics 2002;111(1):40-5.
2002: Niina Paunu; Päivi Lahermo; Päivi Onkamo; Vesa Ollikainen; Immo Rantala; Pauli Helén; Kalle O J Simola; Juha Kere; Hannu Haapasalo
A novel low-penetrance locus for familial glioma at 15q23-q26.3.
Cancer research 2002;62(13):3798-802.
2002: Juha Kere; Outi Elomaa
Healing a natural knockout of epithelial organogenesis.
Trends in molecular medicine 2002;8(5):197-200.
2002: Hannes Lohi; Minna Kujala; Siru Makela; Eero Lehtonen; Marjo Kestila; Ulpu Saarialho-Kere; Daniel Markovich; Juha Kere
Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9.
The Journal of biological chemistry 2002;277(16):14246-54.
2002: Sebsebe Lemeta; Yan Aalto; Mika Niemelä; Juha Jääskeläinen; Markku Sainio; Juha Kere; Sakari Knuutila; Tom Böhling
Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma.
Cancer genetics and cytogenetics 2002;133(2):174-8.
2002: Heikki Mannila; Anne Patrikainen; Jouni K Seppänen; Juha Kere
Long-range control of expression in yeast.
Bioinformatics (Oxford, England) 2002;18(3):482-3.
2002: Katariina Hannula; Marita Lipsanen-Nyman; Paula Kristo; Ilkka Kaitila; Kalle O J Simola; Hanna-Liisa Lenko; Päivi Tapanainen; Christer Holmberg; Juha Kere
Genetic screening for maternal uniparental disomy of chromosome 7 in prenatal and postnatal growth retardation of unknown cause.
Pediatrics 2002;109(3):441-8.
2002: Kati Asumalahti; Colin Veal; Tarja Laitinen; Sari Suomela; Michael Allen; Outi Elomaa; Michael Moser; Rafael de Cid; Samuli Ripatti; Igor Vorechovsky; Jan A Marcusson; Hidemi Nakagawa; Conxi Lazaro; Xavier Estivill; Francesca Capon; Giuseppe Novelli; Ulpu Saarialho-Kere; Jonathan Barker; Richard C Trembath; Juha Kere
Coding haplotype analysis supports HCR as the putative susceptibility gene for psoriasis at the MHC PSORS1 locus.
Human molecular genetics 2002;11(5):589-97.
2002: Petra Jacob; Heidi Rossmann; Georg Lamprecht; Alexandra Kretz; Christina Neff; Elena Lin-Wu; Michael Gregor; David A Groneberg; Juha Kere; Ursula Seidler
Down-regulated in adenoma mediates apical Cl-/HCO3- exchange in rabbit, rat, and human duodenum.
Gastroenterology 2002;122(3):709-24.
2002: Marjut Ranki-Pesonen; Juha Kere
[The gene behind asthma has been found--or has it?].
Duodecim; lääketieteellinen aikakauskirja 2002;118(20):2061-3.
2002: Marko Salmenkivi; Juha Kere; Heikki Mannila
Genome segmentation using piecewise constant intensity models and reversible jump MCMC.
Bioinformatics (Oxford, England) 2002;18 Suppl 2():S211-8.
2001: Maija Hytönen; M Patjas; Seija I Vento; Pekka E Kauppi; Henrik Malmberg; Jukka Ylikoski; Juha Kere
Cystic fibrosis gene mutations deltaF508 and 394delTT in patients with chronic sinusitis in Finland.
Acta oto-laryngologica 2001;121(8):945-7.
2001: Rosa B Barkardottir; Laura Sarantaus; Adalgeir Arason; Paula Vehmanen; P O Bendahl; Tommi Kainu; Kirsi Syrjäkoski; Ralf Krahe; Pia Huusko; Seppo Pyrhönen; Kaija Holli; Olli Kallioniemi; Valgardur Egilsson; Juha Kere; Heli Nevanlinna
Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families.
European journal of human genetics : EJHG 2001;9(10):773-9.
2001: Hannele Koillinen; FK Wong; Jorma Rautio; Vesa Ollikainen; Agneta Karsten; Ola Larson; Bin Tean Teh; Jan Huggare; Päivi Lahermo; Catharina Larsson; Juha Kere
Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
European journal of human genetics : EJHG 2001;9(10):747-52.
2001: Jaana Nopola-Hemmi; Birgitta Myllyluoma; Tuomas Haltia; Mikko Taipale; Vesa Ollikainen; Timo Ahonen; Arja Voutilainen; Juha Kere; Elisabeth Widén
A dominant gene for developmental dyslexia on chromosome 3.
Journal of medical genetics 2001;38(10):658-64.
2001: Pekka E Kauppi; Kerstin Lindblad-Toh; Petteri Sevon; Hannu Toivonen; JD Rioux; A Villapakkam; Lauri A Laitinen; Thomas J Hudson; Juha Kere; Tarja Laitinen
A second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma.
Genomics 2001;77(1-2):35-42.
2001: E Virolainen; Katri Niemi; Agneta Gånemo; Juha Kere; Anders Vahlquist; Ulpu Saarialho-Kere
Ultrastructural features resembling those of harlequin ichthyosis in patients with severe congenital ichthyosiform erythroderma.
The British journal of dermatology 2001;145(3):480-3.
2001: Pia Höglund; M Sormaala; S Haila; J Socha; U Rajaram; W Scheurlen; M Sinaasappel; H de Jonge; Christer Holmberg; H Yoshikawa; Juha Kere
Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea.
Human mutation 2001;18(3):233-42.
2001: S Haila; Johanna Hästbacka; T Böhling; Marja-Liisa Karjalainen-Lindsberg; Juha Kere; Ulpu Saarialho-Kere
SLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell types.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2001;49(8):973-82.
2001: Tarja Laitinen; Mark J Daly; JD Rioux; Pekka E Kauppi; C Laprise; Tuula Petäys; T Green; M Cargill; Tari Haahtela; Eric S Lander; Lauri A Laitinen; Thomas J Hudson; Juha Kere
A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population.
Nature genetics 2001;28(1):87-91.
2001: Outi Elomaa; K Pulkkinen; Ulf Hannelius; Marja L Mikkola; Ulpu Saarialho-Kere; Juha Kere
Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein.
Human molecular genetics 2001;10(9):953-62.
2001: Katariina Hannula; Juha Kere; S Pirinen; Christer Holmberg; Marita Lipsanen-Nyman
Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?
Journal of medical genetics 2001;38(4):273-8.
2001: Katariina Hannula; Marita Lipsanen-Nyman; S W Scherer; Christer Holmberg; Pia Höglund; Juha Kere
Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA.
Genomics 2001;73(1):1-9.
2001: Sari Koskenmies; Elisabeth Widen; Juha Kere; Heikki Julkunen
Familial systemic lupus erythematosus in Finland.
The Journal of rheumatology 2001;28(4):758-60.
2001: Kimmo Pääkkönen; Stefano Cambiaghi; G Novelli; L V Ouzts; Maila Penttinen; Juha Kere; Anand K Srivastava
The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia.
Human mutation 2001;17(4):349.
2001: Ying Zhu; Anu Loukola; Outi Monni; K Kuokkanen; Kaarle Franssila; Erkki Elonen; Juhani Vilpo; Heikki Joensuu; Juha Kere; L Aaltonen; Sakari Knuutila
PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas.
Leukemia & lymphoma 2001;41(1-2):177-83.
2001: FK Wong; Hannele Koillinen; Jorma Rautio; Bin Tean Teh; Reijo Ranta; Agneta Karsten; Ola Larson; Sten Linder-Aronson; Jan Huggare; Catharina Larsson; Juha Kere
Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.
Journal of medical genetics 2001;38(3):198-202.
2001: Kimmo Pääkkönen; S Sauramo; Laura Sarantaus; Pia Vahteristo; A Hartikainen; Paula Vehmanen; Jaakko Ignatius; Vesa Ollikainen; Helena Kääriäinen; E Vauramo; Heli Nevanlinna; Ralf Krahe; Kaija Holli; Juha Kere
Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population.
Genetic epidemiology 2001;20(2):239-46.
2001: Petteri Sevon; Vesa Ollikainen; Päivi Onkamo; Hannu Toivonen; Heikki Mannila; Juha Kere
Mining associations between genetic markers, phenotypes, and covariates.
Genetic epidemiology 2001;21 Suppl 1():S588-93.
2001: S Kiuru-Kuhlefelt; Wa'el El-Rifai; J Fanburg-Smith; Juha Kere; Markku Miettinen; Sakari Knuutila
Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans.
Cytogenetics and cell genetics 2001;92(3-4):192-5.
2001: Katariina Hannula; Marita Lipsanen-Nyman; T Kontiokari; Juha Kere
A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.
American journal of human genetics 2001;68(1):247-53.
2000: Hannes Lohi; Minna Kujala; Erja Kerkelä; Ulpu Saarialho-Kere; Marjo Kestilä; Juha Kere
Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger.
Genomics 2000;70(1):102-12.
2000: O Rechardt; Outi Elomaa; MO Vaalamo; Kimmo Pääkkönen; Tiina Jahkola; Johanna Höök-Nikanne; R M Hembry; Lari Häkkinen; Juha Kere; Ulpu Saarialho-Kere
Stromelysin-2 is upregulated during normal wound repair and is induced by cytokines.
The Journal of investigative dermatology 2000;115(5):778-87.
2000: Pekka E Kauppi; Tarja Laitinen; Vesa Ollikainen; Heikki Mannila; Lauri A Laitinen; Juha Kere
The IL9R region contribution in asthma is supported by genetic association in an isolated population.
European journal of human genetics : EJHG 2000;8(10):788-92.
2000: Laura Sarantaus; Pia Huusko; Hannaleena Eerola; Virpi Launonen; Paula Vehmanen; Katrin Rapakko; Elizabeth M Gillanders; Kirsi Syrjäkoski; Tommi Kainu; Pia Vahteristo; Ralf Krahe; Kimmo Pääkkönen; J Hartikainen; Carl Blomqvist; T Löppönen; Kaija Holli; Markku Ryynänen; Ralf Bützow; Ake Borg; B Wasteson Arver; E Holmberg; Arto Mannermaa; Juha Kere; Olli Kallioniemi; Robert Winqvist; Heli Nevanlinna
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland.
European journal of human genetics : EJHG 2000;8(10):757-63.
2000: Hanna Huopio; Frank Reimann; R Ashfield; Jorma Komulainen; H L Lenko; Jacques Rahier; Ilkka Vauhkonen; Juha Kere; Markku Laakso; Frances M Ashcroft; Timo Otonkoski
Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.
The Journal of clinical investigation 2000;106(7):897-906.
2000: Jaana Nopola-Hemmi; Mikko Taipale; Tuomas Haltia; Anna-Elina Lehesjoki; Arja Voutilainen; Juha Kere
Two translocations of chromosome 15q associated with dyslexia.
Journal of medical genetics 2000;37(10):771-5.
2000: Hannu Toivonen; Päivi Onkamo; K Vasko; Vesa Ollikainen; Petteri Sevon; Heikki Mannila; M Herr; Juha Kere
Data mining applied to linkage disequilibrium mapping.
American journal of human genetics 2000;67(1):133-45.
2000: Kati Asumalahti; Tarja Laitinen; R Itkonen-Vatjus; Marja-Liisa Lokki; Sari Suomela; Erna Snellman; Ulpu Saarialho-Kere; Juha Kere
A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele.
Human molecular genetics 2000;9(10):1533-42.
2000: Mika Niemelä; Sebsebe Lemeta; Markku Sainio; S Rauma; E Pukkala; Juha Kere; Tom Böhling; Leila Laatikainen; Juha Jääskeläinen; Paula Summanen
Hemangioblastomas of the retina: impact of von Hippel-Lindau disease.
Investigative ophthalmology & visual science 2000;41(7):1909-15.
2000: Juha Kere; Pia Höglund
Inherited disorders of ion transport in the intestine.
Current opinion in genetics & development 2000;10(3):306-9.
2000: S Haila; Ulpu Saarialho-Kere; Marja-Liisa Karjalainen-Lindsberg; Hannes Lohi; Karri Airola; Christer Holmberg; Johanna Hästbacka; Juha Kere; Pia Höglund
The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells.
Histochemistry and cell biology 2000;113(4):279-86.
2000: Tarja Laitinen; Vesa Ollikainen; Conxi Lázaro; Pekka E Kauppi; Rafael de Cid; Josep M Antó; Xavier Estivill; H Lokki; Heikki Mannila; Lauri A Laitinen; Juha Kere
Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders.
American journal of respiratory and critical care medicine 2000;161(3 Pt 1):700-6.
2000: E Virolainen; Maija Wessman; Iiris Hovatta; Katri Niemi; Jaakko Ignatius; Juha Kere; Leena Peltonen; Aarno Palotie
Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.
American journal of human genetics 2000;66(3):1132-7.
2000: Stefano Cambiaghi; Lucia Restano; Kimmo Pääkkönen; Ruggero Caputo; Juha Kere
Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia.
Archives of dermatology 2000;136(2):217-24.
1999: Johanna Pispa; Han-Sung Jung; Jukka Jernvall; Päivi Kettunen; Tuija Mustonen; M J Tabata; Juha Kere; Irma Thesleff
Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF.
Developmental biology 1999;216(2):521-34.
1999: AM Björkqvist; M Wolf; Stig Nordling; Lauri Tammilehto; Aija Knuuttila; Juha Kere; Karin Mattson; Sakari Knuutila
Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis.
British journal of cancer 1999;81(7):1111-5.
1999: Marja L Mikkola; Johanna Pispa; Mari Pekkanen; L Paulin; Pekka Nieminen; Juha Kere; Irma Thesleff
Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion.
Mechanisms of development 1999;88(2):133-46.
1999: S Ezer; M Bayés; Outi Elomaa; David Schlessinger; Juha Kere
Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells.
Human molecular genetics 1999;8(11):2079-86.
1999: E Laiho; Katri Niemi; Jaakko Ignatius; Juha Kere; Aarno Palotie; Ulpu Saarialho-Kere
Clinical and morphological correlations for transglutaminase 1 gene mutations in autosomal recessive congenital ichthyosis.
European journal of human genetics : EJHG 1999;7(6):625-32.
1999: Paula Salmikangas; O M Mykkänen; Mikaela Grönholm; Leena Heiska; Juha Kere; Olli Carpén
Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy.
Human molecular genetics 1999;8(7):1329-36.
1999: Timo Otonkoski; C Ammälä; Hanna Huopio; Gilbert J Cote; J Chapman; Karen E Cosgrove; R Ashfield; E Huang; Jorma Komulainen; Frances M Ashcroft; Mark J Dunne; Juha Kere; Pamela M Thomas
A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
Diabetes 1999;48(2):408-15.
1999: Pia Höglund; Christer Holmberg; S Haila; Albert de La Chapelle; Juha Kere
[Congenital chloride diarrhea gene error in the anion transporter protein].
Duodecim; lääketieteellinen aikakauskirja 1999;115(17):1833-41.
1999: Mika Niemelä; Sebsebe Lemeta; Paula Summanen; Tom Böhling; Markku Sainio; Juha Kere; Kristiina Poussa; Risto Sankila; Hannu Haapasalo; H Kääriäinen; E Pukkala; Juha Jääskeläinen
Long-term prognosis of haemangioblastoma of the CNS: impact of von Hippel-Lindau disease.
Acta neurochirurgica 1999;141(11):1147-56.
1999: Richard H Moseley; Pia Höglund; Gary D Wu; Debra G Silberg; S Haila; Albert de La Chapelle; Christer Holmberg; Juha Kere
Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea.
The American journal of physiology 1999;276(1 Pt 1):G185-92.
1999: Juha Kere; Hannes Lohi; Pia Höglund
Genetic Disorders of Membrane Transport III. Congenital chloride diarrhea.
The American journal of physiology 1999;276(1 Pt 1):G7-G13.
1998: P Majander-Nordenswan; Markku Sainio; O Turunen; Juha Jääskeläinen; Olli Carpén; Juha Kere; Antti Vaheri
Genomic structure of the human ezrin gene.
Human genetics 1998;103(6):662-5.
1998: Pekka E Kauppi; Lauri A Laitinen; Harri Laitinen; Juha Kere; Tarja Laitinen
Verification of self-reported asthma and allergy in subjects and their family members volunteering for gene mapping studies.
Respiratory medicine 1998;92(11):1281-8.
1998: M Bayés; Andrew Hartung; S Ezer; Johanna Pispa; Irma Thesleff; Anand K Srivastava; Juha Kere
The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats.
Human molecular genetics 1998;7(11):1661-9.
1998: Pia Höglund; Mari Auranen; J Socha; K Popinska; H Nazer; U Rajaram; A Al Sanie; M Al-Ghanim; Christer Holmberg; Albert de La Chapelle; Juha Kere
Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait.
American journal of human genetics 1998;63(3):760-8.
1998: O Montonen; S Ezer; Johanna Laurikkala; Marja-Liisa Karjalainen-Lindsberg; Irma Thesleff; Juha Kere; Ulpu Saarialho-Kere
Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin.
Experimental dermatology 1998;7(4):168-74.
1998: S Haila; Pia Höglund; S W Scherer; J R Lee; Paula Kristo; Beth Coyle; Richard C Trembath; Christer Holmberg; Albert de La Chapelle; Juha Kere
Genomic structure of the human congenital chloride diarrhea (CLD) gene.
Gene 1998;214(1-2):87-93.
1998: Pekka E Kauppi; Lauri A Laitinen; Harri Laitinen; Juha Kere; Tarja Laitinen
Phenotyping asthma patients for a gene mapping study in Finland.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 1998;28 Suppl 1():40-2; discussion 65-6.
1998: MO Vaalamo; Marja-Liisa Karjalainen-Lindsberg; Pauli Puolakkainen; Juha Kere; Ulpu Saarialho-Kere
Distinct expression profiles of stromelysin-2 (MMP-10), collagenase-3 (MMP-13), macrophage metalloelastase (MMP-12), and tissue inhibitor of metalloproteinases-3 (TIMP-3) in intestinal ulcerations.
The American journal of pathology 1998;152(4):1005-14.
1998: Karri Airola; Matti Ahonen; Nina Johansson; P Heikkilä; Juha Kere; Veli-Matti Kähäri; Ulpu Saarialho-Kere
Human TIMP-3 is expressed during fetal development, hair growth cycle, and cancer progression.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1998;46(4):437-47.
1998: O Montonen; S Ezer; Ulpu Saarialho-Kere; Riitta Herva; Marja-Liisa Karjalainen-Lindsberg; I Kaitila; David Schlessinger; Anand K Srivastava; Irma Thesleff; Juha Kere
The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1998;46(3):281-9.
1998: Pia Höglund; S Haila; K H Gustavson; Mikko Taipale; Katariina Hannula; K Popinska; Christer Holmberg; J Socha; Albert de La Chapelle; Juha Kere
Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.
Human mutation 1998;11(4):321-7.
1997: S Kiuru-Kuhlefelt; Paula Kristo; Tapani Ruutu; Sakari Knuutila; Juha Kere
Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm.
Leukemia 1997;11(12):2097-104.
1997: Anand K Srivastava; Johanna Pispa; Andrew Hartung; Y Du; S Ezer; T Jenks; T Shimada; Mari Pekkanen; Marja L Mikkola; Minoru S H Ko; Irma Thesleff; Juha Kere; David Schlessinger
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(24):13069-74.
1997: Tarja Laitinen; Pekka E Kauppi; Jaakko Ignatius; T Ruotsalainen; Mark J Daly; Helena Kääriäinen; L Kruglyak; Harri Laitinen; ALBERT DE LA CHAPELLE; Eric S Lander; Lauri A Laitinen; Juha Kere
Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.
Human molecular genetics 1997;6(12):2069-76.
1997: E Laiho; Jaakko Ignatius; H Mikkola; Vivien C Yee; David C Teller; Katri Niemi; Ulpu Saarialho-Kere; Juha Kere; Aarno Palotie
Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.
American journal of human genetics 1997;61(3):529-38.
1997: S Ezer; David Schlessinger; A Srivastava; Juha Kere
Anhidrotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding.
Human molecular genetics 1997;6(9):1581-7.
1996: Pia Höglund; S Haila; J Socha; L Tomaszewski; Ulpu Saarialho-Kere; Marja-Liisa Karjalainen-Lindsberg; Karri Airola; Christer Holmberg; Albert de La Chapelle; Juha Kere
Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea.
Nature genetics 1996;14(3):316-9.
1996: Juha Kere; Anand K Srivastava; O Montonen; Jonathan (Jon) Zonana; N Thomas; Betsy M Ferguson; F Munoz; D Morgan; A Clarke; P Baybayan; E Y Chen; S Ezer; Ulpu Saarialho-Kere; Albert de La Chapelle; David Schlessinger
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.
Nature genetics 1996;13(4):409-16.
1996: MO Vaalamo; M Weckroth; P Puolakkainen; Juha Kere; P Saarinen; J Lauharanta; Ulpu Saarialho-Kere
Patterns of matrix metalloproteinase and TIMP-1 expression in chronic and normally healing human cutaneous wounds.
The British journal of dermatology 1996;135(1):52-9.
1996: Pia Höglund; S Haila; Stephen W Scherer; Lap-Chee Tsui; Eric Green; J Weissenbach; Christer Holmberg; Albert de La Chapelle; Juha Kere
Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31.
Genome research 1996;6(3):202-10.
1996: Juha Kere; Olli Kallioniemi
[From pedigree analysis to gene defects].
Duodecim; lääketieteellinen aikakauskirja 1996;112(4):297-305.
1996: Juha Kere; L Palotie
[About the effect of HUGO (Human Genome Project)].
Duodecim; lääketieteellinen aikakauskirja 1996;112(4):291-3.
1996: Anand K Srivastava; O Montonen; Ulpu Saarialho-Kere; E Chen; P Baybayan; Johanna Pispa; J Limon; David Schlessinger; Juha Kere
Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed.
American journal of human genetics 1996;58(1):126-32.
1995: Pia Höglund; Pertti Sistonen; Reijo Norio; Christer Holmberg; A Dimberg; Karl-Henrik Gustavson; Albert de La Chapelle; Juha Kere
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.
American journal of human genetics 1995;57(1):95-102.
1994: Pia Höglund; Christer Holmberg; Albert de La Chapelle; Juha Kere
Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.
American journal of human genetics 1994;55(4):747-52.
1994: Ramaiah Nagaraja; Juha Kere; Sandra MacMillan; M J Masisi; D Johnson; B J Molini; G R Halley; K Wein; M Trusgnich; B Eble
Characterization of four human YAC libraries for clone size, chimerism and X chromosome sequence representation.
Nucleic acids research 1994;22(16):3406-11.
1994: Juha Kere; Xavier Estivill; M Chillón; N Morral; Virginia Nunes; Reijo Norio; E Savilahti; Albert de La Chapelle
Cystic fibrosis in a low-incidence population: two major mutations in Finland.
Human genetics 1994;93(2):162-6.
1994: Matti Ristola; Juha Kere; Tapani Ruutu; Heikki Repo
Reactive oxygen species of neutrophils from patients with monosomy 7 in the bone marrow: contradictory chemiluminescence activity by whole blood or by purified cells.
European journal of haematology 1994;52(1):28-34.
1993: Juha Kere; Pertti Sistonen; Christer Holmberg; Albert de La Chapelle
The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(22):10686-9.
1993: S Koskinen; T Onnelainen; Albert de La Chapelle; Juha Kere
A rare reciprocal translocation (12;21) segregating for nine generations.
Human genetics 1993;92(5):509-12.
1993: Juha Kere; K H Grzeschik; J Limon; M Gremaud; David Schlessinger; ALBERT DE LA CHAPELLE
Anhidrotic ectodermal dysplasia gene region cloned in yeast artificial chromosomes.
Genomics 1993;16(2):305-10.
1992: Juha Kere; Ramaiah Nagaraja; Steven Mumm; Alfredo Ciccodicola; Michele D'Urso; David Schlessinger
Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts.
Genomics 1992;14(2):241-8.
1992: Albert de La Chapelle; R Tolvanen; G Boysen; J Santavy; L Bleeker-Wagemakers; C P J Maury; Juha Kere
Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187.
Nature genetics 1992;2(2):157-60.
1992: Päivi Peltomäki; Pertti Sistonen; Jukka-Pekka Mecklin; Liisa Pylkkänen; Lauri A Aaltonen; S Nordling; Juha Kere; Heikki Järvinen; Stanley R Hamilton; G Petersen
Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.
Cancer research 1992;52(16):4530-3.
1992: C P J Maury; Juha Kere; R Tolvanen; Albert de La Chapelle
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.
Genomics 1992;13(3):902-3.
1992: Albert de La Chapelle; Juha Kere; GEORGE SACK; R Tolvanen; C P J Maury
Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family.
Genomics 1992;13(3):898-901.
1992: R Mazzarella; V Montanaro; Juha Kere; R Reinbold; Alfredo Ciccodicola; Michele D'Urso; David Schlessinger
Conserved sequence-tagged sites: a phylogenetic approach to genome mapping.
Proceedings of the National Academy of Sciences of the United States of America 1992;89(9):3681-5.
1992: A K Srivastava; V Montanaro; Juha Kere
Simplified template preparation and improved direct sequencing using Taq polymerase.
PCR methods and applications 1992;1(4):255-6.
1992: Marjaana Tiainen; Juha Kere; Lauri Tammilehto; Karin Mattson; Sakari Knuutila
Abnormalities of chromosomes 7 and 22 in human malignant pleural mesothelioma: correlation between Southern blot and cytogenetic analyses.
Genes, chromosomes & cancer 1992;4(2):176-82.
1991: David Schlessinger; R D Little; D Freije; fatima abidi; Ileana Zucchi; G Porta; Giuseppe Pilia; Ramaiah Nagaraja; S K Johnson; J Y Yoon; A Srivastava; Juha Kere; G Palmieri; Alfredo Ciccodicola; V Montanaro; G Romano; Amelia Casamassimi; Michele D'Urso
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28.
Genomics 1991;11(4):783-93.
1991: Tomi Mäkelä; Juha Kere; R Winqvist; Kari Alitalo
Intrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancer.
Molecular and cellular biology 1991;11(8):4015-21.
1991: Juha Kere; R Tolvanen; H Donis-Keller; Albert de La Chapelle
Refinement of human chromosome 7 map around the pro alpha 2(I)collagen gene by long-range restriction mapping.
Nucleic acids research 1991;19(10):2755-9.
1990: C P J Maury; Juha Kere; R Tolvanen; Albert de La Chapelle
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.
FEBS letters 1990;276(1-2):75-7.
1990: Juha Kere; A Ritvanen; Eino Marttinen; Ilkka Kaitila
Craniofrontonasal dysostosis: variable expression in a three-generation family.
Clinical genetics 1990;38(6):441-6.
1990: Juha Kere; E Savilahti; Reijo Norio; Xavier Estivill; Albert de La Chapelle
Cystic fibrosis mutation delta F508 in Finland: other mutations predominate.
Human genetics 1990;85(4):413-5.
1989: Juha Kere; Reijo Norio; E Savilahti; Xavier Estivill; Albert de La Chapelle
Cystic fibrosis in Finland: a molecular and genealogical study.
Human genetics 1989;83(1):20-5.
1989: Juha Kere
Chromosome 7 long arm deletion breakpoints in preleukemia: mapping by pulsed field gel electrophoresis.
Nucleic acids research 1989;17(4):1511-20.
1989: Juha Kere; H Donis-Keller; Tapani Ruutu; Albert de La Chapelle
Chromosome 7 long-arm deletions in myeloid disorders: terminal DNA sequences are commonly conserved and breakpoints vary.
Cytogenetics and cell genetics 1989;50(4):226-9.
1989: Juha Kere; Tapani Ruutu; K A Davies; I B Roninson; P C Watkins; R Winqvist; Albert de La Chapelle
Chromosome 7 long arm deletion in myeloid disorders: a narrow breakpoint region in 7q22 defined by molecular mapping.
Blood 1989;73(1):230-4.
1988: Juha Kere; Sakari Knuutila; Tapani Ruutu; R Leskinen; Albert de La Chapelle
Monocytic involvement by monosomy 7 preceded acute myelomonocytic leukemia in a patient with myelodysplastic syndrome.
Leukemia 1988;2(2):69-73.
1987: Juha Kere; Tapani Ruutu; R Lahtinen; Albert de La Chapelle
Molecular characterization of chromosome 7 long arm deletions in myeloid disorders.
Blood 1987;70(5):1349-53.
1987: M Lindlöf; Juha Kere; Matti Ristola; Heikki Repo; Marjatta Leirisalo-Repo; Harriet von Koskull; P Ammälä; Albert de La Chapelle
Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
Genomics 1987;1(1):87-92.