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Gail Billingsley

Research Profile

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TOP 3
Gail Billingsley; Catherine Deveault; Ajoy Vincent; Elise Héon
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly.
Gail Billingsley; Catherine Deveault; Elise Héon
BBS mutational analysis: a strategic approach.
Catherine Deveault; Gail Billingsley; Jacque L Duncan; Jenea Bin; Rebecca Theal; Ajoy Vincent; Karen J Fieggen; Christina Gerth; Nima Noordeh; Elias I Traboulsi; Gerald A Fishman; David Chitayat; Tanja Knueppel; José M Millán; Francis L Munier; Debra Kennedy; Samuel G Jacobson; A Micheil Innes; Grant A Mitchell; Kym Boycott; Elise Héon
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition.

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All Publications

2012: Gail Billingsley; Catherine Deveault; Ajoy Vincent; Elise Héon
Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly.
Ophthalmic genetics 2012;33(3):150-4.
2011: Gail Billingsley; Catherine Deveault; Elise Héon
BBS mutational analysis: a strategic approach.
Ophthalmic genetics 2011;32(3):181-7.
2011: Catherine Deveault; Gail Billingsley; Jacque L Duncan; Jenea Bin; Rebecca Theal; Ajoy Vincent; Karen J Fieggen; Christina Gerth; Nima Noordeh; Elias I Traboulsi; Gerald A Fishman; David Chitayat; Tanja Knueppel; José M Millán; Francis L Munier; Debra Kennedy; Samuel G Jacobson; A Micheil Innes; Grant A Mitchell; Kym Boycott; Elise Héon
BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition.
Human mutation 2011;32(6):610-9.
2011: Ajoy Vincent; Tom Wright; Gail Billingsley; Carol A Westall; Elise Héon
Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders.
Ophthalmic genetics 2011;32(2):107-13.
2010: Gail Billingsley; Jenea Bin; Karen J Fieggen; Jacque L Duncan; Christina Gerth; Koji Ogata; Shoshana S Wodak; Elias I Traboulsi; Gerald A Fishman; Andrew Paterson; David Chitayat; Tanja Knueppel; José M Millán; Grant A Mitchell; Catherine Deveault; Elise Héon
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population.
Journal of medical genetics 2010;47(7):453-63.
2009: Jenea Bin; Jagadeesan Madhavan; Walter Ferrini; Calvin A Mok; Gail Billingsley; Elise Héon
BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population.
Human mutation 2009;30(7):E737-46.
2006: Gail Billingsley; Sathiyavedu T Santhiya; Andrew D Paterson; Koji Ogata; Shoshana J Wodak; S Mohsen Hosseini; Shyam Manohar Manisastry; Perumalsamy Vijayalakshmi; Puthiya M Gopinath; Jochen Graw; Elise Héon
CRYBA4, a novel human cataract gene, is also involved in microphthalmia.
American journal of human genetics 2006;79(4):702-9.
2006: Andrea L Vincent; Gail Billingsley; Megan Priston; Thomas M Glaser; Edward Oliver; Mike Walter; Robert Ritch; Alex Levin; Elise Heon
Further support of the role of CYP1B1 in patients with Peters anomaly.
Molecular vision 2006;12():506-10.
2005: Colin Willoughby; Ayad Shafiq; Walter Ferrini; Louie Loh Yen Chan; Gail Billingsley; Megan Priston; Calvin Mok; Arvind Chandna; Stephen Kaye; Elise Héon
CRYBB1 mutation associated with congenital cataract and microcornea.
Molecular vision 2005;11():587-93.
2004: Colin Willoughby; Louie Loh Yen Chan; Sarah Herd; Gail Billingsley; Nima Noordeh; Alex V Levin; Yvonne M Buys; Graham E Trope; Mansoor Sarfarazi; Elise Héon
Defining the pathogenicity of optineurin in juvenile open-angle glaucoma.
Investigative ophthalmology & visual science 2004;45(9):3122-30.
2003: Colin Willoughby; Sara Arab; R Gandhi; Sirous Zeinali; Seddigheh Arab; D Luk; Gail Billingsley; Francis L Munier; Elise Héon
A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract.
Journal of medical genetics 2003;40(11):e124.
2003: Norman Klopp; Elise Héon; Gail Billingsley; Thomas Illig; Matthias Wjst; Günther Rudolph; Jochen Graw
Further genetic heterogeneity for autosomal dominant human sutural cataracts.
Ophthalmic research 2003;35(2):71-7.
2002: Elise Héon; Alex Greenberg; Kelly K Kopp; David S Rootman; Andrea L Vincent; Gail Billingsley; Megan Priston; Kimberley M Dorval; Robert L Chow; Roderick R McInnes; Godfrey Heathcote; Carol A Westall; John E Sutphin; Elena V Semina; Rod Bremner; Edwin M Stone
VSX1: a gene for posterior polymorphous dystrophy and keratoconus.
Human molecular genetics 2002;11(9):1029-36.
2002: Andrea L Vincent; Gail Billingsley; Yvonne M Buys; Alex V Levin; Megan Priston; Graham E Trope; Donna Williams-Lyn; Elise Héon
Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.
American journal of human genetics 2002;70(2):448-60.
2001: Andrea L Vincent; Gail Billingsley; Megan Priston; Donna Williams-Lyn; J Sutherland; Thomas M Glaser; Edward R Oliver; M A Walter; G Heathcote; A Levin; Elise Héon
Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.
Journal of medical genetics 2001;38(5):324-6.
2001: Elise Héon; Andrew D Paterson; M Fraser; Gail Billingsley; Megan Priston; Aubin Balmer; Daniel F Schorderet; A Verner; T J Hudson; Francis L Munier
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.
American journal of human genetics 2001;68(3):772-7.
2000: Farideh Mirzayans; Douglas B Gould; Elise Héon; Gail Billingsley; Joanne C Cheung; AJ Mears; Michael A Walter
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.
European journal of human genetics : EJHG 2000;8(1):71-4.
2000: D Gill; R Klose; Francis L Munier; M McFadden; Megan Priston; Gail Billingsley; N Ducrey; Daniel F Schorderet; Elise Héon
Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.
Investigative ophthalmology & visual science 2000;41(1):159-65.
1999: Elise Héon; Megan Priston; Daniel F Schorderet; Gail Billingsley; P O Girard; N Lubsen; Francis L Munier
The gamma-crystallins and human cataracts: a puzzle made clearer.
American journal of human genetics 1999;65(5):1261-7.
1998: Elise Héon; S Liu; Gail Billingsley; O Bernasconi; C Tsilfidis; Daniel F Schorderet; Francis L Munier; C Tsifildis
Gene localization for aculeiform cataract, on chromosome 2q33-35.
American journal of human genetics 1998;63(3):921-6.