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Juha Kere

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Geographic Areas

Finland

Physiology

Concepts & Ideas

Procedures

Genes & Molecular Sequences

Anatomy

Chromosomes, Human, Pair 7

Chemicals & Drugs

Disorders

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Publications

TOP 3
Koskinen L L E; Einarsdottir E; Korponay-Szabo I R; Kurppa K; Kaukinen K; Sistonen P; Pocsai Z; Széles G; Adány R; Mäki M; Kere J; Saavalainen P
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.
Zucchelli Marco; Torkvist Leif; Bresso Francesca; Halfvarson Jonas; Hellquist Anna; Anedda Francesca; Assadi Ghazaleh; Lindgren Gunnar B; Svanfeldt Monika; Janson Martin; Noble Colin L; Pettersson Sven; Lappalainen Maarit; Paavola-Sakki Paulina; Halme Leena; Färkkilä Martti; Turunen Ulla; Satsangi Jack; Kontula Kimmo; Löfberg Robert; Kere Juha; D'Amato Mauro
PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.
Hellquist Anna; Järvinen Tiina M; Koskenmies Sari; Zucchelli Marco; Orsmark-Pietras Christina; Berglind Linda; Panelius Jaana; Hasan Taina; Julkunen Heikki; D'Amato Mauro; Saarialho-Kere Ulpu; Kere Juha
Evidence for genetic association and interaction between the TYK2 and IRF5 genes in systemic lupus erythematosus.

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All Publications

2009: Koskinen L L E; Einarsdottir E; Korponay-Szabo I R; Kurppa K; Kaukinen K; Sistonen P; Pocsai Z; Széles G; Adány R; Mäki M; Kere J; Saavalainen P
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.
Tissue antigens 2009;74(5):408-16.
2009: Zucchelli Marco; Torkvist Leif; Bresso Francesca; Halfvarson Jonas; Hellquist Anna; Anedda Francesca; Assadi Ghazaleh; Lindgren Gunnar B; Svanfeldt Monika; Janson Martin; Noble Colin L; Pettersson Sven; Lappalainen Maarit; Paavola-Sakki Paulina; Halme Leena; Färkkilä Martti; Turunen Ulla; Satsangi Jack; Kontula Kimmo; Löfberg Robert; Kere Juha; D'Amato Mauro
PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.
Inflammatory bowel diseases 2009;15(10):1562-9.
2009: Hellquist Anna; Järvinen Tiina M; Koskenmies Sari; Zucchelli Marco; Orsmark-Pietras Christina; Berglind Linda; Panelius Jaana; Hasan Taina; Julkunen Heikki; D'Amato Mauro; Saarialho-Kere Ulpu; Kere Juha
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: Massinen Satu; Tammimies Kristiina; Tapia-Páez Isabel; Matsson Hans; Hokkanen Marie-Estelle; Söderberg Ola; Landegren Ulf; Castrén Eero; Gustafsson Jan-Ake; Treuter Eckardt; Kere Juha
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
Human molecular genetics 2009;18(15):2802-12.
2009: Peterson H; Laivuori H; Kerkelä E; Jiao H; Hiltunen L; Heino S; Tiala I; Knuutila S; Rasi V; Kere J; Kivinen K
ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.
Molecular human reproduction 2009;15(7):443-9.
2009: Zucchelli Marco; Torkvist Leif; Bresso Francesca; Halfvarson Jonas; Söderhäll Cilla; Lee Young-Ae; Löfberg Robert; Kere Juha; D'Amato Mauro
No association between the eczema genes COL29A1 and IL31 and inflammatory bowel disease.
Inflammatory bowel diseases 2009;15(7):961-2.
2009: Hiltunen Leena M; Laivuori Hannele; Rautanen Anna; Kaaja Risto; Kere Juha; Krusius Tom; Paunio Mikko; Rasi Vesa
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: Dahdouh Faten; Anthoni Heidi; Tapia-Páez Isabel; Peyrard-Janvid Myriam; Schulte-Körne Gerd; Warnke Andreas; Remschmidt Helmut; Ziegler Andreas; Kere Juha; Müller-Myhsok Bertram; Nöthen Markus M; Schumacher Johannes; Zucchelli Marco
Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Psychiatric genetics 2009;19(2):59-63.
2009: Koskinen Lotta L E; Einarsdottir Elisabet; Dukes Emma; Heap Graham A R; Dubois Patrick; Korponay-Szabo Ilma R; Kaukinen Katri; Kurppa Kalle; Ziberna Fabiana; Vatta Serena; Not Tarcisio; Ventura Alessandro; Sistonen Pertti; Adány Róza; Pocsai Zsuzsa; Széles György; Mäki Markku; Kere Juha; Wijmenga Cisca; van Heel David A; Saavalainen Päivi
Association study of the IL18RAP locus in three European populations with coeliac disease.
Human molecular genetics 2009;18(6):1148-55.
2009: Bruce S; Nyberg F; Melén E; James A; Pulkkinen V; Orsmark-Pietras C; Bergström A; Dahlén B; Wickman M; von Mutius E; Doekes G; Lauener R; Riedler J; Eder W; van Hage M; Pershagen G; Scheynius A; Kere J
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: Bruce Sara; Hannula-Jouppi Katariina; Peltonen Jari; Kere Juha; Lipsanen-Nyman Marita
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: Kainu Kati; Kivinen Katja; Zucchelli Marco; Suomela Sari; Kere Juha; Inerot Annica; Baker Barbara S; Powles Anne V; Fry Lionel; Samuelsson Lena; Saarialho-Kere Ulpu
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: He Huiling; Nagy Rebecca; Liyanarachchi Sandya; Jiao Hong; Li Wei; Suster Saul; Kere Juha; de la Chapelle Albert
A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24.
Cancer research 2009;69(2):625-31.
2009: Lappalainen T; Hannelius U; Salmela E; von Döbeln U; Lindgren C M; Huoponen K; Savontaus M-L; Kere J; Lahermo P
Population structure in contemporary Sweden--a Y-chromosomal and mitochondrial DNA analysis.
Annals of human genetics 2009;73(1):61-73.
2009: Suomela Sari; Elomaa Outi; Skoog Tiina; Ala-aho Risto; Jeskanen Leila; Pärssinen Jenita; Latonen Leena; Grénman Reidar; Kere Juha; Kähäri Veli-Matti; Saarialho-Kere Ulpu
CCHCR1 is up-regulated in skin cancer and associated with EGFR expression.
PloS one 2009;4(6):e6030.
2009: Ekelund Elisabeth; Bradley Maria; Weidinger Stephan; Jovanovic Dragan L; Johansson Catharina; Lindgren Cecilia M; Todorova Antonia; Jakob Thilo; Illig Thomas; von Mutius Erika; Braun-Fahrländer Charlotte; Doekes Gert; Riedler Josef; Scheynius Annika; Pershagen Göran; Kockum Ingrid; Kere Juha
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: Einarsdottir Elisabet; Koskinen Lotta L E; Dukes Emma; Kainu Kati; Suomela Sari; Lappalainen Maarit; Ziberna Fabiana; Korponay-Szabo Ilma R; Kurppa Kalle; Kaukinen Katri; Adány Róza; Pocsai Zsuzsa; Széles György; Färkkilä Martti; Turunen Ulla; Halme Leena; Paavola-Sakki Paulina; Not Tarcisio; Vatta Serena; Ventura Alessandro; Löfberg Robert; Torkvist Leif; Bresso Francesca; Halfvarson Jonas; Mäki Markku; Kontula Kimmo; Saarialho-Kere Ulpu; Kere Juha; D'Amato Mauro; Saavalainen Päivi
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.
2008: Ludwig Kerstin U; Schumacher Johannes; Schulte-Körne Gerd; König Inke R; Warnke Andreas; Plume Ellen; Anthoni Heidi; Peyrard-Janvid Myriam; Meng Haiying; Ziegler Andreas; Remschmidt Helmut; Kere Juha; Gruen Jeffrey R; Müller-Myhsok Bertram; Nöthen Markus M; Hoffmann Per
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: Jiao Hong; Tóth Beáta; Erdos Melinda; Fransson Ingegerd; Rákóczi Eva; Balogh István; Magyarics Zoltán; Dérfalvi Beáta; Csorba Gabriella; Szaflarska Anna; Megarbane Andre; Akatcherian Carlo; Dbaibo Ghassan; Rajnavölgyi Eva; Hammarström Lennart; Kere Juha; Lefranc Gérard; Maródi László
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
Molecular immunology 2008;46(1):202-6.
2008: Wedenoja Satu; Ormälä Timo; Berg Ulla B; Halling Stella F Edström; Jalanko Hannu; Karikoski Riitta; Kere Juha; Holmberg Christer; Höglund Pia
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: Melén Erik; Nyberg Fredrik; Lindgren Cecilia M; Berglind Niklas; Zucchelli Marco; Nordling Emma; Hallberg Jenny; Svartengren Magnus; Morgenstern Ralf; Kere Juha; Bellander Tom; Wickman Magnus; Pershagen Göran
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: Tapia-Páez Isabel; Tammimies Kristiina; Massinen Satu; Roy Ananda L; Kere Juha
The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2008;22(8):3001-9.
2008: Orsmark-Pietras Christina; Melén Erik; Vendelin Johanna; Bruce Sara; Laitinen Annika; Laitinen Lauri A; Lauener Roger; Riedler Josef; von Mutius Erika; Doekes Gert; Wickman Magnus; van Hage Marianne; Pershagen Göran; Scheynius Annika; Nyberg Fredrik; Kere Juha;
Biological and genetic interaction between tenascin C and neuropeptide S receptor 1 in allergic diseases.
Human molecular genetics 2008;17(11):1673-82.
2008: Jiao H; Kaaman M; Dungner E; Kere J; Arner P; Dahlman I
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: Pegelow M; Peyrard-Janvid M; Zucchelli M; Fransson I; Larson O; Kere J; Larsson C; Karsten A
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: Tiala Inkeri; Wakkinen Janica; Suomela Sari; Puolakkainen Pauli; Tammi Raija; Forsberg Sofi; Rollman Ola; Kainu Kati; Rozell Björn; Kere Juha; Saarialho-Kere Ulpu; Elomaa Outi
The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice.
Human molecular genetics 2008;17(7):1043-51.
2008: Koskinen L L E; Korponay-Szabo I R; Viiri K; Juuti-Uusitalo K; Kaukinen K; Lindfors K; Mustalahti K; Kurppa K; Adány R; Pocsai Z; Széles G; Einarsdottir E; Wijmenga C; Mäki M; Partanen J; Kere J; Saavalainen P
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: Siljander Tuula; Karppelin Matti; Vähäkuopus Susanna; Syrjänen Jaana; Toropainen Maija; Kere Juha; Vuento Risto; Jussila Tapio; Vuopio-Varkila Jaana
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: Bruce Sara; Hannula-Jouppi Katariina; Lindgren Cecilia M; Lipsanen-Nyman Marita; Kere Juha
Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR.
Clinical chemistry 2008;54(3):491-9.
2008: Salmela Elina; Lappalainen Tuuli; Fransson Ingegerd; Andersen Peter M; Dahlman-Wright Karin; Fiebig Andreas; Sistonen Pertti; Savontaus Marja-Liisa; Schreiber Stefan; Kere Juha; Lahermo Päivi
Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.
PloS one 2008;3(10):e3519.
2008: Hannelius Ulf; Salmela Elina; Lappalainen Tuuli; Guillot Gilles; Lindgren Cecilia M; von Döbeln Ulrika; Lahermo Päivi; Kere Juha
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: Zhang Pu; Dixon Morag; Zucchelli Marco; Hambiliki Fredwell; Levkov Lev; Hovatta Outi; Kere Juha
Expression analysis of the NLRP gene family suggests a role in human preimplantation development.
PloS one 2008;3(7):e2755.
2007: Barone Sharon; Amlal Hassane; Kujala Minna; Xu Jie; Karet Fiona; Blanchard Ann; Kere Juha; Soleimani Manoocher
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: D'Amato Mauro; Bruce Sara; Bresso Francesca; Zucchelli Marco; Ezer Sini; Pulkkinen Ville; Lindgren Cecilia; Astegiano Marco; Rizzetto Mario; Gionchetti Paolo; Riegler Gabriele; Sostegni Raffaello; Daperno Marco; D'Alfonso Sandra; Momigliano-Richiardi Patricia; Torkvist Leif; Puolakkainen Pauli; Lappalainen Maarit; Paavola-Sakki Paulina; Halme Leena; Farkkila Martti; Turunen Ulla; Kontula Kimmo; Lofberg Robert; Pettersson Sven; Kere Juha
Neuropeptide s receptor 1 gene polymorphism is associated with susceptibility to inflammatory bowel disease.
Gastroenterology 2007;133(3):808-17.
2007: Otonkoski Timo; Jiao Hong; Kaminen-Ahola Nina; Tapia-Paez Isabel; Ullah Mohammed S; Parton Laura E; Schuit Frans; Quintens Roel; Sipilä Ilkka; Mayatepek Ertan; Meissner Thomas; Halestrap Andrew P; Rutter Guy A; Kere Juha
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: Lee-Kirsch Min Ae; Gong Maolian; Chowdhury Dipanjan; Senenko Lydia; Engel Kerstin; Lee Young-Ae; de Silva Udesh; Bailey Suzanna L; Witte Torsten; Vyse Timothy J; Kere Juha; Pfeiffer Christiane; Harvey Scott; Wong Andrew; Koskenmies Sari; Hummel Oliver; Rohde Klaus; Schmidt Reinhold E; Dominiczak Anna F; Gahr Manfred; Hollis Thomas; Perrino Fred W; Lieberman Judy; Hübner Norbert
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: Hannelius Ulf; Gherman Loreana; Mäkelä Ville-Veikko; Lindstedt Astrid; Zucchelli Marco; Lagerberg Camilla; Tybring Gunnel; Kere Juha; Lindgren Cecilia M
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: Ollikainen M; Hannelius U; Lindgren C M; Abdel-Rahman W M; Kere J; Peltomäki P
Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach.
Oncogene 2007;26(31):4541-9.
2007: Dahlman Ingrid; Dicker Andrea; Jiao Hong; Kere Juha; Blomqvist Lennart; van Harmelen Vanessa; Hoffstedt Johan; Borch-Johnsen Knut; Jorgensen Torben; Hansen Torben; Pedersen Oluf; Laakso Markku; Arner Peter
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: Tiala Inkeri; Suomela Sari; Huuhtanen Jari; Wakkinen Janica; Hölttä-Vuori Maarit; Kainu Kati; Ranta Sirpa; Turpeinen Ursula; Hämäläinen Esa; Jiao Hong; Karvonen Seija-Liisa; Ikonen Elina; Kere Juha; Saarialho-Kere Ulpu; Elomaa Outi
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: Hellquist Anna; Zucchelli Marco; Kivinen Katja; Saarialho-Kere Ulpu; Koskenmies Sari; Widen Elisabeth; Julkunen Heikki; Wong Andrew; Karjalainen-Lindsberg Marja-Liisa; Skoog Tiina; Vendelin Johanna; Cunninghame-Graham Deborah S; Vyse Timothy J; Kere Juha; Lindgren Cecilia M
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: Pylkäs Katri; Tommiska Johanna; Syrjäkoski Kirsi; Kere Juha; Gatei Magtouf; Waddell Nicola; Allinen Minna; Karppinen Sanna-Maria; Rapakko Katrin; Kääriäinen Helena; Aittomäki Kristiina; Blomqvist Carl; Mustonen Aki; Holli Kaija; Khanna Kum Kum; Kallioniemi Olli-Pekka; Nevanlinna Heli; Winqvist Robert
Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer.
Carcinogenesis 2007;28(5):1040-5.
2007: Kujala Minna; Hihnala Satu; Tienari Jukka; Kaunisto Kari; Hästbacka Johanna; Holmberg Christer; Kere Juha; Höglund Pia
Expression of ion transport-associated proteins in human efferent and epididymal ducts.
Reproduction (Cambridge, England) 2007;133(4):775-84.
2007: Kivinen Katja; Peterson Hanna; Hiltunen Leena; Laivuori Hannele; Heino Sanna; Tiala Inkeri; Knuutila Sakari; Rasi Vesa; Kere Juha
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: Anthoni Heidi; Zucchelli Marco; Matsson Hans; Müller-Myhsok Bertram; Fransson Ingegerd; Schumacher Johannes; Massinen Satu; Onkamo Päivi; Warnke Andreas; Griesemann Heide; Hoffmann Per; Nopola-Hemmi Jaana; Lyytinen Heikki; Schulte-Körne Gerd; Kere Juha; Nöthen Markus M; Peyrard-Janvid Myriam
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: Erkko Hannele; Xia Bing; Nikkilä Jenni; Schleutker Johanna; Syrjäkoski Kirsi; Mannermaa Arto; Kallioniemi Anne; Pylkäs Katri; Karppinen Sanna-Maria; Rapakko Katrin; Miron Alexander; Sheng Qing; Li Guilan; Mattila Henna; Bell Daphne W; Haber Daniel A; Grip Mervi; Reiman Mervi; Jukkola-Vuorinen Arja; Mustonen Aki; Kere Juha; Aaltonen Lauri A; Kosma Veli-Matti; Kataja Vesa; Soini Ylermi; Drapkin Ronny I; Livingston David M; Winqvist Robert
A recurrent mutation in PALB2 in Finnish cancer families.
Nature 2007;446(7133):316-9.
2007: Zhang Pu; Kerkelä Erja; Skottman Heli; Levkov Lev; Kivinen Katja; Lahesmaa Riitta; Hovatta Outi; Kere Juha
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: Kerkelä Erja; Skottman Heli; Friden Barbro; Bjuresten Kerstin; Kere Juha; Hovatta Outi
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: Lu Shasha; Zhao Chen; Jiao Hong; Kere Juha; Tang Xin; Zhao Feng; Zhang Xiumei; Zhao Kanxing; Larsson Catharina
Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations.
Molecular vision 2007;13():1154-60.
2007: Kere Juha
[Not Available]
Duodecim; lääketieteellinen aikakauskirja 2007;123(8):864-6.
2007: Orsmark Christina; Skoog Tiina; Jeskanen Leila; Kere Juha; Saarialho-Kere Ulpu
Expression of allograft inflammatory factor-1 in inflammatory skin disorders.
Acta dermato-venereologica 2007;87(3):223-7.
2007: Suomela Sari; Kainu Kati; Onkamo Päivi; Tiala Inkeri; Himberg Johan; Koskinen Lotta; Snellman Erna; Karvonen Seija-Liisa; Karvonen Jaakko; Uurasmaa Tutta; Reunala Timo; Kivikäs Kristiina; Jansén Christer T; Holopainen Päivi; Elomaa Outi; Kere Juha; Saarialho-Kere Ulpu
Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.
Acta dermato-venereologica 2007;87(2):127-34.
2007: Hiltunen Leena; Rautanen Anna; Rasi Vesa; Kaaja Risto; Kere Juha; Krusius Tom; Vahtera Elina; Paunio Mikko
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: Dahlman Ingrid; Nilsson Maria; Jiao Hong; Hoffstedt Johan; Lindgren Cecilia M; Humphreys Keith; Kere Juha; Gustafsson Jan-Ake; Arner Peter; Dahlman-Wright Karin
Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity.
Pharmacogenetics and genomics 2006;16(12):881-9.
2006: Melén E; Umerkajeff S; Nyberg F; Zucchelli M; Lindstedt A; Gullstén H; Wickman M; Pershagen G; Kere J
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: Feuk Lars; Kalervo Aino; Lipsanen-Nyman Marita; Skaug Jennifer; Nakabayashi Kazuhiko; Finucane Brenda; Hartung Danielle; Innes Micheil; Kerem Batsheva; Nowaczyk Malgorzata J; Rivlin Joseph; Roberts Wendy; Senman Lili; Summers Anne; Szatmari Peter; Wong Virginia; Vincent John B; Zeesman Susan; Osborne Lucy R; Cardy Janis Oram; Kere Juha; Scherer Stephen W; Hannula-Jouppi Katariina
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.
American journal of human genetics 2006;79(5):965-72.
2006: Rautanen Anna; Eriksson Johan G; Kere Juha; Andersson Sture; Osmond Clive; Tienari Pentti; Sairanen Heikki; Barker David J P; Phillips David I W; Forsén Tom; Kajantie Eero
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: Karppinen S-M; Barkardottir R B; Backenhorn K; Sydenham T; Syrjäkoski K; Schleutker J; Ikonen T; Pylkäs K; Rapakko K; Erkko H; Johannesdottir G; Gerdes A-M; Thomassen M; Agnarsson B A; Grip M; Kallioniemi A; Kere J; Aaltonen L A; Arason A; Møller P; Kruse T A; Borg A; Winqvist R
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: Vendelin Johanna; Bruce Sara; Holopainen Päivi; Pulkkinen Ville; Rytilä Paula; Pirskanen Asta; Rehn Marko; Laitinen Tarja; Laitinen Lauri A; Haahtela Tari; Saarialho-Kere Ulpu; Laitinen Annika; Kere Juha
Downstream target genes of the neuropeptide S-NPSR1 pathway.
Human molecular genetics 2006;15(19):2923-35.
2006: Zintzaras Elias; Kitsios Georgios; Harrison Gavan A; Laivuori Hannele; Kivinen Katja; Kere Juha; Messinis Ioannis; Stefanidis Ioannis; Ioannidis John P A
Heterogeneity-based genome search meta-analysis for preeclampsia.
Human genetics 2006;120(3):360-70.
2006: Lahermo Päivi; Liljedahl Ulrika; Alnaes Grethe; Axelsson Tomas; Brookes Anthony J; Ellonen Pekka; Groop Per-Henrik; Halldén Christer; Holmberg Dan; Holmberg Kristina; Keinänen Mauri; Kepp Katrin; Kere Juha; Kiviluoma Päivi; Kristensen Vessela; Lindgren Cecilia; Odeberg Jacob; Osterman Pia; Parkkonen Maija; Saarela Janna; Sterner Maria; Strömqvist Linda; Talas Ulvi; Wessman Maija; Palotie Aarno; Syvänen Ann-Christine
A quality assessment survey of SNP genotyping laboratories.
Human mutation 2006;27(7):711-4.
2006: Hodgson Ulla; Pulkkinen Ville; Dixon Morag; Peyrard-Janvid Myriam; Rehn Marko; Lahermo Paivi; Ollikainen Vesa; Salmenkivi Kaisa; Kinnula Vuokko; Kere Juha; Tukiainen Pentti; Laitinen Tarja
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.
American journal of human genetics 2006;79(1):149-54.
2006: Salmela E; Taskinen O; Seppänen J K; Sistonen P; Daly M J; Lahermo P; Savontaus M-L; Kere J
Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.
Journal of medical genetics 2006;43(7):590-7.
2006: Ekelund E; Saaf A; Tengvall-Linder M; Melen E; Link J; Barker J; Reynolds N J; Meggitt S J; Kere J; Wahlgren C-F; Pershagen G; Wickman M; Nordenskjold M; Kockum I; Bradley M
Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis.
American journal of human genetics 2006;78(6):1060-5.
2006: De Jager P L; Graham R; Farwell L; Sawcer S; Richardson A; Behrens T W; Compston A; Hafler D A; Kere J; Vyse T J; Rioux J D
The role of inflammatory bowel disease susceptibility loci in multiple sclerosis and systemic lupus erythematosus.
Genes and immunity 2006;7(4):327-34.
2006: Pulkkinen Ville; Majuri Marja-Leena; Wang Guoying; Holopainen Päivi; Obase Yasushi; Vendelin Johanna; Wolff Henrik; Rytilä Paula; Laitinen Lauri A; Haahtela Tari; Laitinen Tarja; Alenius Harri; Kere Juha; Rehn Marko
Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses.
Human molecular genetics 2006;15(10):1667-79.
2006: Smedby Karin Ekström; Lindgren Cecilia M; Hjalgrim Henrik; Humphreys Keith; Schöllkopf Claudia; Chang Ellen T; Roos Göran; Ryder Lars P; Falk Kerstin I; Palmgren Juni; Kere Juha; Melbye Mads; Glimelius Bengt; Adami Hans-Olov
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: Hihnala S; Kujala M; Toppari J; Kere J; Holmberg C; Höglund P
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: Sillén A; Forsell C; Lilius L; Axelman K; Björk B F; Onkamo P; Kere J; Winblad B; Graff C
Genome scan on Swedish Alzheimer's disease families.
Molecular psychiatry 2006;11(2):182-6.
2006: Schumacher Johannes; Anthoni Heidi; Dahdouh Faten; König Inke R; Hillmer Axel M; Kluck Nadine; Manthey Malou; Plume Ellen; Warnke Andreas; Remschmidt Helmut; Hülsmann Jutta; Cichon Sven; Lindgren Cecilia M; Propping Peter; Zucchelli Marco; Ziegler Andreas; Peyrard-Janvid Myriam; Schulte-Körne Gerd; Nöthen Markus M; Kere Juha
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
American journal of human genetics 2006;78(1):52-62.
2006: Kere Juha
Overview of the SLC26 family and associated diseases.
Novartis Foundation symposium 2006;273():2-11; discussion 11-8, 261-4.
2006: Pulkkinen Ville; Haataja Ritva; Hannelius Ulf; Helve Otto; Pitkänen Olli M; Karikoski Riitta; Rehn Marko; Marttila Riitta; Lindgren Cecilia M; Hästbacka Johanna; Andersson Sture; Kere Juha; Hallman Mikko; Laitinen Tarja
G protein-coupled receptor for asthma susceptibility associates with respiratory distress syndrome.
Annals of medicine 2006;38(5):357-66.
2005: Peyrard-Janvid Myriam; Pegelow Marie; Koillinen Hannele; Larsson Catharina; Fransson Ingegerd; Rautio Jorma; Hukki Jyri; Larson Ola; Karsten Agneta L-A; Kere Juha
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: Rautanen Anna; Zucchelli Marco; Mäkelä Siru; Kere Juha
Gene mapping with pooled samples on three genotyping platforms.
Molecular and cellular probes 2005;19(6):408-16.
2005: Kinnunen Satu; Bonache Sandra; Casals Teresa; Monto Sanni; Savilahti Erkki; Kere Juha; Järvelä Irma
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: Bruce S; Leinonen R; Lindgren C M; Kivinen K; Dahlman-Wright K; Lipsanen-Nyman M; Hannula-Jouppi K; Kere J
Global analysis of uniparental disomy using high density genotyping arrays.
Journal of medical genetics 2005;42(11):847-51.
2005: Jiao Hong; Dahlman Ingrid; Eriksson Per; Kere Juha; Arner Peter
A common beta2-adrenoceptor gene haplotype protects against obesity in Swedish women.
Obesity research 2005;13(10):1645-50.
2005: Hannula-Jouppi Katariina; Kaminen-Ahola Nina; Taipale Mikko; Eklund Ranja; Nopola-Hemmi Jaana; Kääriäinen Helena; Kere Juha
The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia.
PLoS genetics 2005;1(4):e50.
2005: Hannelius U; Lindgren C M; Melén E; Malmberg A; von Dobeln U; Kere J
Phenylketonuria screening registry as a resource for population genetic studies.
Journal of medical genetics 2005;42(10):e60.
2005: Dahlman Ingrid; Kaaman Maria; Jiao Hong; Kere Juha; Laakso Markku; Arner Peter
The CIDEA gene V115F polymorphism is associated with obesity in Swedish subjects.
Diabetes 2005;54(10):3032-4.
2005: Vendelin Johanna; Pulkkinen Ville; Rehn Marko; Pirskanen Asta; Räisänen-Sokolowski Anne; Laitinen Annika; Laitinen Lauri A; Kere Juha; Laitinen Tarja
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: Veal Colin D; Reynolds Nick J; Meggitt Simon J; Allen Michael H; Lindgren Cecilia M; Kere Juha; Trembath Richard C; Barker Jonathan N W N
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: Kere Juha
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: Wu Hui; Cantor Rita M; Graham Deborah S Cunninghame; Lingren Cecilia M; Farwell Lisa; Jager Philip L De; Bottini Nunzio; Grossman Jennifer M; Wallace Daniel J; Hahn Bevra H; Julkunen Heikki; Hebert Lee A; Rovin Brad H; Birmingham Dan J; Rioux John D; Yu C Yung; Kere Juha; Vyse Timothy J; Tsao Betty P
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: Sankelo Marja; Flanagan Julia A; Machado Rajiv; Harrison Rachel; Rudarakanchana Nung; Morrell Nicholas; Dixon Morag; Halme Maija; Puolijoki Hannu; Kere Juha; Elomaa Outi; Kupari Markku; Räisänen-Sokolowski Anne; Trembath Richard C; Laitinen Tarja
BMPR2 mutations have short lifetime expectancy in primary pulmonary hypertension.
Human mutation 2005;26(2):119-24.
2005: Holmkvist Johan; Almgren Peter; Parikh Hemang; Zucchelli Marco; Kere Juha; Groop Leif; Lindgren Cecilia M
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: Swanberg Maria; Lidman Olle; Padyukov Leonid; Eriksson Per; Akesson Eva; Jagodic Maja; Lobell Anna; Khademi Mohsen; Börjesson Ola; Lindgren Cecilia M; Lundman Pia; Brookes Anthony J; Kere Juha; Luthman Holger; Alfredsson Lars; Hillert Jan; Klareskog Lars; Hamsten Anders; Piehl Fredrik; Olsson Tomas
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: Melén Erik; Bruce Sara; Doekes Gert; Kabesch Michael; Laitinen Tarja; Lauener Roger; Lindgren Cecilia M; Riedler Josef; Scheynius Annika; van Hage-Hamsten Marianne; Kere Juha; Pershagen Göran; Wickman Magnus; Nyberg Fredrik;
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: Sigurdsson Snaevar; Nordmark Gunnel; Göring Harald H H; Lindroos Katarina; Wiman Ann-Christin; Sturfelt Gunnar; Jönsen Andreas; Rantapää-Dahlqvist Solbritt; Möller Bozena; Kere Juha; Koskenmies Sari; Widén Elisabeth; Eloranta Maija-Leena; Julkunen Heikki; Kristjansdottir Helga; Steinsson Kristjan; Alm Gunnar; Rönnblom Lars; Syvänen Ann-Christine
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: Chernova Marina N; Jiang Lianwei; Friedman David J; Darman Rachel B; Lohi Hannes; Kere Juha; Vandorpe David H; Alper Seth L
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: Koillinen H; Lahermo P; Rautio J; Hukki J; Peyrard-Janvid M; Kere J
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: Mäkelä S; Eklund R; Lähdetie J; Mikkola M; Hovatta O; Kere J
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: Pykäläinen Maritta; Kinos Riikka; Valkonen Sanna; Rydman Pia; Kilpeläinen Maritta; Laitinen Lauri A; Karjalainen Jussi; Nieminen Markku; Hurme Mikko; Kere Juha; Laitinen Tarja; Lahesmaa Riitta
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: Ylisaukko-Oja Tero; Peyrard-Janvid Myriam; Lindgren Cecilia M; Rehnström Karola; Vanhala Raija; Peltonen Leena; Järvelä Irma; Kere Juha
Family-based association study of DYX1C1 variants in autism.
European journal of human genetics : EJHG 2005;13(1):127-30.
2005: Kere Juha
Mapping genes for asthma and psoriasis.
Novartis Foundation symposium 2005;267():46-52; discussion 52-6.
2005: Kujala Minna; Tienari Jukka; Lohi Hannes; Elomaa Outi; Sariola Hannu; Lehtonen Eero; Kere Juha
SLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidney.
Nephron. Experimental nephrology 2005;101(2):e50-8.
2004: Melén E; Gullstén H; Zucchelli M; Lindstedt A; Nyberg F; Wickman M; Pershagen G; Kere J
Sex specific protective effects of interleukin-9 receptor haplotypes on childhood wheezing and sensitisation.
Journal of medical genetics 2004;41(12):e123.
2004: Kere Juha; Laitinen Tarja
Positionally cloned susceptibility genes in allergy and asthma.
Current opinion in immunology 2004;16(6):689-94.
2004: Dahlman I; Eriksson P; Kaaman M; Jiao H; Lindgren C M; Kere J; Arner P
alpha2-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action.
Diabetologia 2004;47(11):1974-9.
2004: Kajantie Eero; Rautanen Anna; Kere Juha; Andersson Sture; Ylihärsilä Hilkka; Osmond Clive; Barker David J P; Forsén Tom; Eriksson Johan
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: Barone Sharon; Amlal Hassane; Xu Jie; Kujala Minna; Kere Juha; Petrovic Snezana; Soleimani Manoocher
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: Elomaa Outi; Majuri Inkeri; Suomela Sari; Asumalahti Kati; Jiao Hong; Mirzaei Zahra; Rozell Bjorn; Dahlman-Wright Karin; Pispa Johanna; Kere Juha; Saarialho-Kere Ulpu
Transgenic mouse models support HCR as an effector gene in the PSORS1 locus.
Human molecular genetics 2004;13(15):1551-61.
2004: Ylikoski E; Kinos R; Sirkkanen N; Pykäläinen M; Savolainen J; Laitinen L A; Kere J; Laitinen T; Lahesmaa R
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: Melén E; Kere J; Pershagen G; Svartengren M; Wickman M
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: Koskenmies Sari; Widén Elisabeth; Onkamo Päivi; Sevón Petteri; Julkunen Heikki; Kere Juha
Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus.
European journal of human genetics : EJHG 2004;12(6):489-94.
2004: Laitinen Tarja; Polvi Anne; Rydman Pia; Vendelin Johanna; Pulkkinen Ville; Salmikangas Paula; Mäkelä Siru; Rehn Marko; Pirskanen Asta; Rautanen Anna; Zucchelli Marco; Gullstén Harriet; Leino Marina; Alenius Harri; Petäys Tuula; Haahtela Tari; Laitinen Annika; Laprise Catherine; Hudson Thomas J; Laitinen Lauri A; Kere Juha
Characterization of a common susceptibility locus for asthma-related traits.
Science (New York, N.Y.) 2004;304(5668):300-4.
2004: Peyrard-Janvid Myriam; Anthoni Heidi; Onkamo Päivi; Lahermo Päivi; Zucchelli Marco; Kaminen Nina; Hannula-Jouppi Katariina; Nopola-Hemmi Jaana; Voutilainen Arja; Lyytinen Heikki; Kere Juha
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Human genetics 2004;114(5):510-6.
2004: Kinnula V L; Lehtonen S; Koistinen P; Kakko S; Savolainen M; Kere J; Ollikainen V; Laitinen T
Two functional variants of the superoxide dismutase genes in Finnish families with asthma.
Thorax 2004;59(2):116-9.
2004: Koskenmies S; Lahermo P; Julkunen H; Ollikainen V; Kere J; Widén E
Linkage mapping of systemic lupus erythematosus (SLE) in Finnish families multiply affected by SLE.
Journal of medical genetics 2004;41(1):e2-5.
2004: Petrovic Snezana; Barone Sharon; Xu Jie; Conforti Laura; Ma Liyun; Kujala Minna; Kere Juha; Soleimani Manoocher
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.
2004: Koskenmies S; Vaarala O; Widen E; Kere J; Palosuo T; Julkunen H
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.
2003: Suomela Sari; Elomaa Outi; Asumalahti Kati; Kariniemi Arja Leena; Karvonen Seija Liisa; Peltonen Juha; Kere Juha; Saarialho-Kere Ulpu
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: Asumalahti Kati; Laitinen Tarja; Lahermo Päivi; Suomela Sari; Itkonen-Vatjus Raija; Jansen Christer; Karvonen Jaakko; Karvonen Seija-Liisa; Reunala Timo; Snellman Erna; Uurasmaa Tutta; Saarialho-Kere Ulpu; Kere Juha
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: Taipale Mikko; Kaminen Nina; Nopola-Hemmi Jaana; Haltia Tuomas; Myllyluoma Birgitta; Lyytinen Heikki; Muller Kurt; Kaaranen Minna; Lindsberg Perttu J; Hannula-Jouppi Katariina; Kere Juha
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: Koillinen H; Ollikainen V; Rautio J; Hukki J; Kere J
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: Petrovic Snezana; Ju Xie; Barone Sharon; Seidler Ursula; Alper Seth L; Lohi Hannes; Kere Juha; Soleimani Manoocher
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: Kaminen N; Hannula-Jouppi K; Kestilä M; Lahermo P; Muller K; Kaaranen M; Myllyluoma B; Voutilainen A; Lyytinen H; Nopola-Hemmi J; Kere J
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: Asumalahti Kati; Ameen Mahreen; Suomela Sari; Hagforsen Eva; Michaëlsson Gerd; Evans Julie; Munro Margo; Veal Colin; Allen Michael; Leman Joyce; David Burden A; Kirby Brian; Connolly Maureen; Griffiths Christopher E M; Trembath Richard C; Kere Juha; Saarialho-Kere Ulpu; Barker Jonathan N W N
Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis.
The Journal of investigative dermatology 2003;120(4):627-32.
2003: Melkoniemi Miia; Koillinen Hannele; Männikkö Minna; Warman Matthew L; Pihlajamaa Tero; Kääriäinen Helena; Rautio Jorma; Hukki Jyri; Stofko Joseph A; Cisneros George J; Krakow Deborah; Cohn Daniel H; Kere Juha; Ala-Kokko Leena
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.
European journal of human genetics : EJHG 2003;11(3):265-70.
2003: Lohi Hannes; Lamprecht Georg; Markovich Daniel; Heil Anders; Kujala Minna; Seidler Ursula; Kere Juha
Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains.
American journal of physiology. Cell physiology 2003;284(3):C769-79.
2003: Otonkoski Timo; Kaminen Nina; Ustinov Jarkko; Lapatto Risto; Meissner Thomas; Mayatepek Ertan; Kere Juha; Sipilä Ilkka
Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release.
Diabetes 2003;52(1):199-204.
2003: Laivuori Hannele; Lahermo Päivi; Ollikainen Vesa; Widen Elisabeth; Häivä-Mällinen Leena; Sundström Helena; Laitinen Tarja; Kaaja Risto; Ylikorkala Olavi; Kere Juha
Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.
American journal of human genetics 2003;72(1):168-77.
2003: Asumalahti Kati; Saarialho-Kere Ulpu; Kere Juha
[The pathogenesis of psoriasis--investigating the genetics of a multifactorial disease]
Duodecim; lääketieteellinen aikakauskirja 2003;119(16):1517-22.
2002: Zhu Ying; Hollmén Jaakko; Räty Riikka; Aalto Yan; Nagy Balint; Elonen Erkki; Kere Juha; Mannila Heikki; Franssila Kaarle; Knuutila Sakari
Investigatory and analytical approaches to differential gene expression profiling in mantle cell lymphoma.
British journal of haematology 2002;119(4):905-15.
2002: Mäkelä Siru; Kere Juha; Holmberg Christer; Höglund Pia
SLC26A3 mutations in congenital chloride diarrhea.
Human mutation 2002;20(6):425-38.
2002: Ahokas Katja; Lohi Jouko; Lohi Hannes; Elomaa Outi; Karjalainen-Lindsberg Marja Liisa; Kere Juha; Saarialho-Kere Ulpu
Matrix metalloproteinase-21, the human orthologue for XMMP, is expressed during fetal development and in cancer.
Gene 2002;301(1-2):31-41.
2002: Onkamo P; Ollikainen V; Sevon P; Toivonen H T T; Mannila H; Kere J
Association analysis for quantitative traits by data mining: QHPM.
Annals of human genetics 2002;66(Pt 5-6):419-29.
2002: Polvi Anne; Polvi Tuomas; Sevon Petteri; Petäys Tuula; Haahtela Tari; Laitinen Lauri A; Kere Juha; Laitinen Tarja
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: Nopola-Hemmi Jaana; Myllyluoma Birgitta; Voutilainen Arja; Leinonen Seija; Kere Juha; Ahonen Timo
Familial dyslexia: neurocognitive and genetic correlation in a large Finnish family.
Developmental medicine and child neurology 2002;44(9):580-6.
2002: Woolley Niina; Holopainen Päivi; Ollikainen Vesa; Mustalahti Kirsi; Mäki Markku; Kere Juha; Partanen Jukka
A new locus for coeliac disease mapped to chromosome 15 in a population isolate.
Human genetics 2002;111(1):40-5.
2002: Paunu Niina; Lahermo Päivi; Onkamo Päivi; Ollikainen Vesa; Rantala Immo; Helén Pauli; Simola Kalle O J; Kere Juha; Haapasalo Hannu
A novel low-penetrance locus for familial glioma at 15q23-q26.3.
Cancer research 2002;62(13):3798-802.
2002: Kere Juha; Elomaa Outi
Healing a natural knockout of epithelial organogenesis.
Trends in molecular medicine 2002;8(5):197-200.
2002: Lohi Hannes; Kujala Minna; Makela Siru; Lehtonen Eero; Kestila Marjo; Saarialho-Kere Ulpu; Markovich Daniel; Kere Juha
Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9.
The Journal of biological chemistry 2002;277(16):14246-54.
2002: Lemeta Sebsebe; Aalto Yan; Niemelä Mika; Jääskeläinen Juha; Sainio Markku; Kere Juha; Knuutila Sakari; Böhling Tom
Recurrent DNA sequence copy losses on chromosomal arm 6q in capillary hemangioblastoma.
Cancer genetics and cytogenetics 2002;133(2):174-8.
2002: Mannila Heikki; Patrikainen Anne; Seppänen Jouni K; Kere Juha
Long-range control of expression in yeast.
Bioinformatics (Oxford, England) 2002;18(3):482-3.
2002: Hannula Katariina; Lipsanen-Nyman Marita; Kristo Paula; Kaitila Ilkka; Simola Kalle O J; Lenko Hanna Liisa; Tapanainen Päivi; Holmberg Christer; Kere Juha
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: Asumalahti Kati; Veal Colin; Laitinen Tarja; Suomela Sari; Allen Michael; Elomaa Outi; Moser Michael; de Cid Rafael; Ripatti Samuli; Vorechovsky Igor; Marcusson Jan A; Nakagawa Hidemi; Lazaro Conxi; Estivill Xavier; Capon Francesca; Novelli Giuseppe; Saarialho-Kere Ulpu; Barker Jonathan; Trembath Richard; Kere Juha;
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: Jacob Petra; Rossmann Heidi; Lamprecht Georg; Kretz Alexandra; Neff Christina; Lin-Wu Elena; Gregor Michael; Groneberg David A; Kere Juha; Seidler Ursula
Down-regulated in adenoma mediates apical Cl-/HCO3- exchange in rabbit, rat, and human duodenum.
Gastroenterology 2002;122(3):709-24.
2002: Ranki-Pesonen Marjut; Kere Juha
[The gene behind asthma has been found--or has it?]
Duodecim; lääketieteellinen aikakauskirja 2002;118(20):2061-3.
2002: Salmenkivi Marko; Kere Juha; Mannila Heikki
Genome segmentation using piecewise constant intensity models and reversible jump MCMC.
Bioinformatics (Oxford, England) 2002;18 Suppl 2():S211-8.
2001: Hytönen M; Patjas M; Vento S I; Kauppi P; Malmberg H; Ylikoski J; Kere J
Cystic fibrosis gene mutations deltaF508 and 394delTT in patients with chronic sinusitis in Finland.
Acta oto-laryngologica 2001;121(8):945-7.
2001: Barkardottir R B; Sarantaus L; Arason A; Vehmanen P; Bendahl P O; Kainu T; Syrjäkoski K; Krahe R; Huusko P; Pyrhönen S; Holli K; Kallioniemi O P; Egilsson V; Kere J; Nevanlinna H
Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families.
European journal of human genetics : EJHG 2001;9(10):773-9.
2001: Koillinen H; Wong F K; Rautio J; Ollikainen V; Karsten A; Larson O; Teh B T; Huggare J; Lahermo P; Larsson C; Kere J
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: Nopola-Hemmi J; Myllyluoma B; Haltia T; Taipale M; Ollikainen V; Ahonen T; Voutilainen A; Kere J; Widén E
A dominant gene for developmental dyslexia on chromosome 3.
Journal of medical genetics 2001;38(10):658-64.
2001: Kauppi P; Lindblad-Toh K; Sevon P; Toivonen H T; Rioux J D; Villapakkam A; Laitinen L A; Hudson T J; Kere J; Laitinen T
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: Virolainen E; Niemi K M; Gånemo A; Kere J; Vahlquist A; Saarialho-Kere U
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: Höglund P; Sormaala M; Haila S; Socha J; Rajaram U; Scheurlen W; Sinaasappel M; de Jonge H; Holmberg C; Yoshikawa H; Kere J
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: Haila S; Hästbacka J; Böhling T; Karjalainen-Lindsberg M L; Kere J; Saarialho-Kere U
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: Laitinen T; Daly M J; Rioux J D; Kauppi P; Laprise C; Petäys T; Green T; Cargill M; Haahtela T; Lander E S; Laitinen L A; Hudson T J; Kere J
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: Hannula K; Kere J; Pirinen S; Holmberg C; Lipsanen-Nyman M
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: Hannula K; Lipsanen-Nyman M; Scherer S W; Holmberg C; Höglund P; Kere J
Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA.
Genomics 2001;73(1):1-9.
2001: Koskenmies S; Widen E; Kere J; Julkunen H
Familial systemic lupus erythematosus in Finland.
The Journal of rheumatology 2001;28(4):758-60.
2001: Elomaa O; Pulkkinen K; Hannelius U; Mikkola M; Saarialho-Kere U; Kere J
Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein.
Human molecular genetics 2001;10(9):953-62.
2001: Pääkkönen K; Cambiaghi S; Novelli G; Ouzts L V; Penttinen M; Kere J; Srivastava A K
The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia.
Human mutation 2001;17(4):349.
2001: Zhu Y; Loukola A; Monni O; Kuokkanen K; Franssila K; Elonen E; Vilpo J; Joensuu H; Kere J; Aaltonen L; Knuutila S
PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas.
Leukemia & lymphoma 2001;41(1-2):177-83.
2001: Wong F K; Koillinen H; Rautio J; Teh B T; Ranta R; Karsten A; Larson O; Linder-Aronson S; Huggare J; Larsson C; Kere J
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: Pääkkönen K; Sauramo S; Sarantaus L; Vahteristo P; Hartikainen A; Vehmanen P; Ignatius J; Ollikainen V; Kääriäinen H; Vauramo E; Nevanlinna H; Krahe R; Holli K; Kere J
Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population.
Genetic epidemiology 2001;20(2):239-46.
2001: Hannula K; Lipsanen-Nyman M; Kontiokari T; Kere J
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.
2001: Sevon P; Ollikainen V; Onkamo P; Toivonen H T; Mannila H; Kere J
Mining associations between genetic markers, phenotypes, and covariates.
Genetic epidemiology 2001;21 Suppl 1():S588-93.
2001: Kiuru-Kuhlefelt S; El-Rifai W; Fanburg-Smith J; Kere J; Miettinen M; Knuutila S
Concomitant DNA copy number amplification at 17q and 22q in dermatofibrosarcoma protuberans.
Cytogenetics and cell genetics 2001;92(3-4):192-5.
2000: Lohi H; Kujala M; Kerkelä E; Saarialho-Kere U; Kestilä M; Kere J
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: Rechardt O; Elomaa O; Vaalamo M; Pääkkönen K; Jahkola T; Höök-Nikanne J; Hembry R M; Häkkinen L; Kere J; Saarialho-Kere U
Stromelysin-2 is upregulated during normal wound repair and is induced by cytokines.
The Journal of investigative dermatology 2000;115(5):778-87.
2000: Kauppi P; Laitinen T; Ollikainen V; Mannila H; Laitinen L A; Kere J
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: Sarantaus L; Huusko P; Eerola H; Launonen V; Vehmanen P; Rapakko K; Gillanders E; Syrjäkoski K; Kainu T; Vahteristo P; Krahe R; Pääkkönen K; Hartikainen J; Blomqvist C; Löppönen T; Holli K; Ryynänen M; Bützow R; Borg A; Wasteson Arver B; Holmberg E; Mannermaa A; Kere J; Kallioniemi O P; Winqvist R; Nevanlinna H
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: Huopio H; Reimann F; Ashfield R; Komulainen J; Lenko H L; Rahier J; Vauhkonen I; Kere J; Laakso M; Ashcroft F; Otonkoski T
Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.
The Journal of clinical investigation 2000;106(7):897-906.
2000: Nopola-Hemmi J; Taipale M; Haltia T; Lehesjoki A E; Voutilainen A; Kere J
Two translocations of chromosome 15q associated with dyslexia.
Journal of medical genetics 2000;37(10):771-5.
2000: Toivonen H T; Onkamo P; Vasko K; Ollikainen V; Sevon P; Mannila H; Herr M; Kere J
Data mining applied to linkage disequilibrium mapping.
American journal of human genetics 2000;67(1):133-45.
2000: Asumalahti K; Laitinen T; Itkonen-Vatjus R; Lokki M L; Suomela S; Snellman E; Saarialho-Kere U; Kere J
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: Niemelä M; Lemeta S; Sainio M; Rauma S; Pukkala E; Kere J; Böhling T; Laatikainen L; Jääskeläinen J; Summanen P
Hemangioblastomas of the retina: impact of von Hippel-Lindau disease.
Investigative ophthalmology & visual science 2000;41(7):1909-15.
2000: Kere J; Höglund P
Inherited disorders of ion transport in the intestine.
Current opinion in genetics & development 2000;10(3):306-9.
2000: Haila S; Saarialho-Kere U; Karjalainen-Lindsberg M L; Lohi H; Airola K; Holmberg C; Hästbacka J; Kere J; Höglund P
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: Laitinen T; Ollikainen V; Lázaro C; Kauppi P; de Cid R; Antó J M; Estivill X; Lokki H; Mannila H; Laitinen L A; Kere J
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: Virolainen E; Wessman M; Hovatta I; Niemi K M; Ignatius J; Kere J; Peltonen L; Palotie A
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: Cambiaghi S; Restano L; Pääkkönen K; Caputo R; Kere J
Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia.
Archives of dermatology 2000;136(2):217-24.
1999: Pispa J; Jung H S; Jernvall J; Kettunen P; Mustonen T; Tabata M J; Kere J; Thesleff I
Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF.
Developmental biology 1999;216(2):521-34.
1999: Björkqvist A M; Wolf M; Nordling S; Tammilehto L; Knuuttila A; Kere J; Mattson K; Knuutila S
Deletions at 14q in malignant mesothelioma detected by microsatellite marker analysis.
British journal of cancer 1999;81(7):1111-5.
1999: Mikkola M L; Pispa J; Pekkanen M; Paulin L; Nieminen P; Kere J; Thesleff I
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: Ezer S; Bayés M; Elomaa O; Schlessinger D; Kere J
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: Laiho E; Niemi K M; Ignatius J; Kere J; Palotie A; Saarialho-Kere U
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: Salmikangas P; Mykkänen O M; Grönholm M; Heiska L; Kere J; Carpén O
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: Otonkoski T; Ammälä C; Huopio H; Cote G J; Chapman J; Cosgrove K; Ashfield R; Huang E; Komulainen J; Ashcroft F M; Dunne M J; Kere J; Thomas P M
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: Moseley R H; Höglund P; Wu G D; Silberg D G; Haila S; de la Chapelle A; Holmberg C; Kere J
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: Kere J; Lohi H; Höglund P
Genetic Disorders of Membrane Transport III. Congenital chloride diarrhea.
The American journal of physiology 1999;276(1 Pt 1):G7-G13.
1999: Höglund P; Holmberg C; Haila S; de la Chapelle A; Kere J
[Congenital chloride diarrhea gene error in the anion transporter protein]
Duodecim; lääketieteellinen aikakauskirja 1999;115(17):1833-41.
1999: Niemelä M; Lemeta S; Summanen P; Böhling T; Sainio M; Kere J; Poussa K; Sankila R; Haapasalo H; Kääriäinen H; Pukkala E; Jääskeläinen J
Long-term prognosis of haemangioblastoma of the CNS: impact of von Hippel-Lindau disease.
Acta neurochirurgica 1999;141(11):1147-56.
1998: Majander-Nordenswan P; Sainio M; Turunen O; Jääskeläinen J; Carpén O; Kere J; Vaheri A
Genomic structure of the human ezrin gene.
Human genetics 1998;103(6):662-5.
1998: Kauppi P; Laitinen L A; Laitinen H; Kere J; Laitinen T
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: Bayés M; Hartung A J; Ezer S; Pispa J; Thesleff I; Srivastava A K; Kere J
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: Höglund P; Auranen M; Socha J; Popinska K; Nazer H; Rajaram U; Al Sanie A; Al-Ghanim M; Holmberg C; de la Chapelle A; Kere J
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: Montonen O; Ezer S; Laurikkala J; Karjalainen-Lindsberg M L; Thesleff I; Kere J; Saarialho-Kere U
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: Haila S; Höglund P; Scherer S W; Lee J R; Kristo P; Coyle B; Trembath R; Holmberg C; de la Chapelle A; Kere J
Genomic structure of the human congenital chloride diarrhea (CLD) gene.
Gene 1998;214(1-2):87-93.
1998: Kauppi P; Laitinen L A; Laitinen H; Kere J; Laitinen T
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: Vaalamo M; Karjalainen-Lindsberg M L; Puolakkainen P; Kere J; Saarialho-Kere U
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: Airola K; Ahonen M; Johansson N; Heikkilä P; Kere J; Kähäri V M; Saarialho-Kere U K
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: Montonen O; Ezer S; Saarialho-Kere U K; Herva R; Karjalainen-Lindsberg M L; Kaitila I; Schlessinger D; Srivastava A K; Thesleff I; Kere J
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: Höglund P; Haila S; Gustavson K H; Taipale M; Hannula K; Popinska K; Holmberg C; Socha J; de la Chapelle A; Kere J
Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene.
Human mutation 1998;11(4):321-7.
1997: Kiuru-Kuhlefelt S; Kristo P; Ruutu T; Knuutila S; Kere J
Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1997;11(12):2097-104.
1997: Srivastava A K; Pispa J; Hartung A J; Du Y; Ezer S; Jenks T; Shimada T; Pekkanen M; Mikkola M L; Ko M S; Thesleff I; Kere J; Schlessinger D
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: Laitinen T; Kauppi P; Ignatius J; Ruotsalainen T; Daly M J; Kääriäinen H; Kruglyak L; Laitinen H; de la Chapelle A; Lander E S; Laitinen L A; Kere J
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: Laiho E; Ignatius J; Mikkola H; Yee V C; Teller D C; Niemi K M; Saarialho-Kere U; Kere J; Palotie A
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: Ezer S; Schlessinger D; Srivastava A; Kere J
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: Höglund P; Haila S; Socha J; Tomaszewski L; Saarialho-Kere U; Karjalainen-Lindsberg M L; Airola K; Holmberg C; de la Chapelle A; Kere J
Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea.
Nature genetics 1996;14(3):316-9.
1996: Kere J; Srivastava A K; Montonen O; Zonana J; Thomas N; Ferguson B; Munoz F; Morgan D; Clarke A; Baybayan P; Chen E Y; Ezer S; Saarialho-Kere U; de la Chapelle A; Schlessinger D
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.
Nature genetics 1996;13(4):409-16.
1996: Vaalamo M; Weckroth M; Puolakkainen P; Kere J; Saarinen P; Lauharanta J; Saarialho-Kere U K
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: Höglund P; Haila S; Scherer S W; Tsui L C; Green E D; Weissenbach J; Holmberg C; de la Chapelle A; Kere J
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: Srivastava A K; Montonen O; Saarialho-Kere U; Chen E; Baybayan P; Pispa J; Limon J; Schlessinger D; Kere J
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.
1996: Kere J; Kallioniemi O P
[From pedigree analysis to gene defects]
Duodecim; lääketieteellinen aikakauskirja 1996;112(4):297-305.
1996: Kere J; Palotie L
[About the effect of HUGO (Human Genome Project)]
Duodecim; lääketieteellinen aikakauskirja 1996;112(4):291-3.
1995: Höglund P; Sistonen P; Norio R; Holmberg C; Dimberg A; Gustavson K H; de la Chapelle A; Kere J
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.
American journal of human genetics 1995;57(1):95-102.
1994: Höglund P; Holmberg C; de la Chapelle A; Kere J
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: Nagaraja R; Kere J; MacMillan S; Masisi M J; Johnson D; Molini B J; Halley G R; Wein K; Trusgnich M; Eble B
Characterization of four human YAC libraries for clone size, chimerism and X chromosome sequence representation.
Nucleic acids research 1994;22(16):3406-11.
1994: Kere J; Estivill X; Chillón M; Morral N; Nunes V; Norio R; Savilahti E; de la Chapelle A
Cystic fibrosis in a low-incidence population: two major mutations in Finland.
Human genetics 1994;93(2):162-6.
1994: Ristola M; Kere J; Ruutu T; Repo H
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: Koskinen S; Onnelainen T; de la Chapelle A; Kere J
A rare reciprocal translocation (12;21) segregating for nine generations.
Human genetics 1993;92(5):509-12.
1993: Kere J; Sistonen P; Holmberg C; de la Chapelle A
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: Kere J; Grzeschik K H; Limon J; Gremaud M; Schlessinger D; de la Chapelle A
Anhidrotic ectodermal dysplasia gene region cloned in yeast artificial chromosomes.
Genomics 1993;16(2):305-10.
1992: Kere J; Nagaraja R; Mumm S; Ciccodicola A; D'Urso M; Schlessinger D
Mapping human chromosomes by walking with sequence-tagged sites from end fragments of yeast artificial chromosome inserts.
Genomics 1992;14(2):241-8.
1992: de la Chapelle A; Tolvanen R; Boysen G; Santavy J; Bleeker-Wagemakers L; Maury C P; Kere J
Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187.
Nature genetics 1992;2(2):157-60.
1992: Peltomäki P; Sistonen P; Mecklin J P; Pylkkänen L; Aaltonen L; Nordling S; Kere J; Järvinen H; Hamilton S R; Petersen G
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: Maury C P; Kere J; Tolvanen R; de la Chapelle A
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.
Genomics 1992;13(3):902-3.
1992: de la Chapelle A; Kere J; Sack G H; Tolvanen R; Maury C P
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: Mazzarella R; Montanaro V; Kere J; Reinbold R; Ciccodicola A; D'Urso M; Schlessinger D
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: Srivastava A K; Montanaro V; Kere J
Simplified template preparation and improved direct sequencing using Taq polymerase.
PCR methods and applications 1992;1(4):255-6.
1992: Tiainen M; Kere J; Tammilehto L; Mattson K; Knuutila S
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: Schlessinger D; Little R D; Freije D; Abidi F; Zucchi I; Porta G; Pilia G; Nagaraja R; Johnson S K; Yoon J Y; Srivastava A; Kere J; Palmieri G; Ciccodicola A; Montanaro V; Romano G; Casamassimi A; D'Urso M
Yeast artificial chromosome-based genome mapping: some lessons from Xq24-q28.
Genomics 1991;11(4):783-93.
1991: Mäkelä T P; Kere J; Winqvist R; Alitalo K
Intrachromosomal rearrangements fusing L-myc and rlf in small-cell lung cancer.
Molecular and cellular biology 1991;11(8):4015-21.
1991: Kere J; Tolvanen R; Donis-Keller H; de la Chapelle A
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: Kere J; Ritvanen A; Marttinen E; Kaitila I
Craniofrontonasal dysostosis: variable expression in a three-generation family.
Clinical genetics 1990;38(6):441-6.
1990: Maury C P; Kere J; Tolvanen R; de la Chapelle A
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.
FEBS letters 1990;276(1-2):75-7.
1990: Kere J; Savilahti E; Norio R; Estivill X; de la Chapelle A
Cystic fibrosis mutation delta F508 in Finland: other mutations predominate.
Human genetics 1990;85(4):413-5.
1989: Kere J; Norio R; Savilahti E; Estivill X; de la Chapelle A
Cystic fibrosis in Finland: a molecular and genealogical study.
Human genetics 1989;83(1):20-5.
1989: Kere J
Chromosome 7 long arm deletion breakpoints in preleukemia: mapping by pulsed field gel electrophoresis.
Nucleic acids research 1989;17(4):1511-20.
1989: Kere J; Ruutu T; Davies K A; Roninson I B; Watkins P C; Winqvist R; de la Chapelle A
Chromosome 7 long arm deletion in myeloid disorders: a narrow breakpoint region in 7q22 defined by molecular mapping.
Blood 1989;73(1):230-4.
1989: Kere J; Donis-Keller H; Ruutu T; de la Chapelle A
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.
1988: Kere J; Knuutila S; Ruutu T; Leskinen R; de la Chapelle A
Monocytic involvement by monosomy 7 preceded acute myelomonocytic leukemia in a patient with myelodysplastic syndrome.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1988;2(2):69-73.
1987: Kere J; Ruutu T; Lahtinen R; de la Chapelle A
Molecular characterization of chromosome 7 long arm deletions in myeloid disorders.
Blood 1987;70(5):1349-53.
1987: Lindlöf M; Kere J; Ristola M; Repo H; Leirisalo-Repo M; von Koskull H; Ammälä P; de la Chapelle A
Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
Genomics 1987;1(1):87-92.

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