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Hannele Koillinen

Research Profile

Disorders

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Chemicals & Drugs

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Finland

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Publications

TOP 3
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.
Maila Penttinen; Hannele Koillinen; Harri Niinikoski; Outi Mäkitie; Marja Hietala
Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalities.
Hannele Koillinen; Satu Jääskeläinen; Kari Koski
[Mitochondrial disorder underlying headache symptoms].

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All Publications

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.
2009: Maila Penttinen; Hannele Koillinen; Harri Niinikoski; Outi Mäkitie; Marja Hietala
Genitopatellar syndrome in an adolescent female with severe osteoporosis and endocrine abnormalities.
American journal of medical genetics. Part A 2009;149A(3):451-5.
2009: Hannele Koillinen; Satu Jääskeläinen; Kari Koski
[Mitochondrial disorder underlying headache symptoms].
Duodecim; lääketieteellinen aikakauskirja 2009;125(3):297-300.
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: 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.
2004: Tarja Linnankivi; Nina Lundbom; Taina Autti; Anna-Maija Häkkinen; Hannele Koillinen; Tuomo Kuusi; Tuula Lönnqvist; Kirsi Sainio; Leena Valanne; Tuula Aärimaa; Helena Pihko
Five new cases of a recently described leukoencephalopathy with high brain lactate.
Neurology 2004;63(4):688-92.
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: 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.
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: 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.