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Julie Hoover-Fong

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 +1.8 Million pre-calculated profiles free of charge to researchers worldwide.

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Sobreira Nara L M; Cirulli Elizabeth T; Avramopoulos Dimitrios; Wohler Elizabeth; Oswald Gretchen L; Stevens Eric L; Ge Dongliang; Shianna Kevin V; Smith Jason P; Maia Jessica M; Gumbs Curtis E; Pevsner Jonathan; Thomas George; Valle David; Hoover-Fong Julie E; Goldstein David B
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
Kaplan Frederick S; Xu Meiqi; Seemann Petra; Connor J Michael; Glaser David L; Carroll Liam; Delai Patricia; Fastnacht-Urban Elisabeth; Forman Stephen J; Gillessen-Kaesbach Gabriele; Hoover-Fong Julie; Köster Bernhard; Pauli Richard M; Reardon William; Zaidi Syed-Adeel; Zasloff Michael; Morhart Rolf; Mundlos Stefan; Groppe Jay; Shore Eileen M
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.
Miller Nathaniel D; Nance Melonie A; Wohler Elizabeth S; Hoover-Fong Julie E; Lisi Emily; Thomas George H; Pevsner Jonathan
Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.

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2010: Sobreira Nara L M; Cirulli Elizabeth T; Avramopoulos Dimitrios; Wohler Elizabeth; Oswald Gretchen L; Stevens Eric L; Ge Dongliang; Shianna Kevin V; Smith Jason P; Maia Jessica M; Gumbs Curtis E; Pevsner Jonathan; Thomas George; Valle David; Hoover-Fong Julie E; Goldstein David B
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
PLoS genetics 2010;6(6):e1000991.
2009: Kaplan Frederick S; Xu Meiqi; Seemann Petra; Connor J Michael; Glaser David L; Carroll Liam; Delai Patricia; Fastnacht-Urban Elisabeth; Forman Stephen J; Gillessen-Kaesbach Gabriele; Hoover-Fong Julie; Köster Bernhard; Pauli Richard M; Reardon William; Zaidi Syed-Adeel; Zasloff Michael; Morhart Rolf; Mundlos Stefan; Groppe Jay; Shore Eileen M
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.
Human mutation 2009;30(3):379-90.
2009: Miller Nathaniel D; Nance Melonie A; Wohler Elizabeth S; Hoover-Fong Julie E; Lisi Emily; Thomas George H; Pevsner Jonathan
Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function.
American journal of medical genetics. Part A 2009;149A(4):669-80.
2009: Hoover-Fong Julie; Savage William J; Lisi Emily; Winkelstein Jerry; Thomas George H; Hoefsloot Lies H; Loeb David M
Congenital T cell deficiency in a patient with CHARGE syndrome.
The Journal of pediatrics 2009;154(1):140-2.
2008: Mardo Veronica; Squibb Elizabeth E; Braverman Nancy; Hoover-Fong Julie E; Migeon Claude; Batista Denise A S; Thomas George H
Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development.
American journal of medical genetics. Part A 2008;146A(17):2293-7.
2008: Hoover-Fong Julie E; Schulze Kerry J; McGready John; Barnes Hillary; Scott Charles I
Age-appropriate body mass index in children with achondroplasia: interpretation in relation to indexes of height.
The American journal of clinical nutrition 2008;88(2):364-71.
2007: Saadeh Reem; Lisi Emily C; Batista Denise A S; McIntosh Iain; Hoover-Fong Julie E
Albinism and developmental delay: the need to test for 15q11-q13 deletion.
Pediatric neurology 2007;37(4):299-302.
2007: Hoover-Fong J E; McGready J; Schulze K J; Barnes H; Scott C I
Weight for age charts for children with achondroplasia.
American journal of medical genetics. Part A 2007;143A(19):2227-35.
2007: Vanscoy Lori L; Blackman Scott M; Collaco Joseph M; Bowers Amanda; Lai Teresa; Naughton Kathleen; Algire Marilyn; McWilliams Rita; Beck Suzanne; Hoover-Fong Julie; Hamosh Ada; Cutler Dave; Cutting Garry R
Heritability of lung disease severity in cystic fibrosis.
American journal of respiratory and critical care medicine 2007;175(10):1036-43.
2006: Blackman Scott M; Deering-Brose Rebecca; McWilliams Rita; Naughton Kathleen; Coleman Barbara; Lai Teresa; Algire Marilyn; Beck Suzanne; Hoover-Fong Julie; Hamosh Ada; Fallin M Daniele; West Kristen; Arking Dan E; Chakravarti Aravinda; Cutler David J; Cutting Garry R
Relative contribution of genetic and nongenetic modifiers to intestinal obstruction in cystic fibrosis.
Gastroenterology 2006;131(4):1030-9.
2006: Cohn Ronald D; Eklund Erik; Bergner Amanda L; Casella James F; Woods S Lee; Althaus Janyne; Blakemore Karin J; Fox Harold E; Hoover-Fong Julie E; Hamosh Ada; Braverman Nancy E; Freeze Hudson H; Boyadjiev Simeon A
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.
Pediatrics 2006;118(2):e514-21.
2005: McIntosh I; Dunston J A; Liu L; Hoover-Fong J E; Sweeney E
Nail patella syndrome revisited: 50 years after linkage.
Annals of human genetics 2005;69(Pt 4):349-63.
2004: Hoover-Fong J E; Shah S; Van Hove J L K; Applegarth D; Toone J; Hamosh A
Natural history of nonketotic hyperglycinemia in 65 patients.
Neurology 2004;63(10):1847-53.
2003: McWilliams Rita; Hoover-Fong Julie; Hamosh Ada; Beck Suzanne; Beaty Terri; Cutting Garry
Problematic variation in local institutional review of a multicenter genetic epidemiology study.
JAMA : the journal of the American Medical Association 2003;290(3):360-6.
2003: Hoover-Fong Julie E; Cai J; Cargile C B; Thomas G H; Patel A; Griffin C A; Jabs E W; Hamosh A
Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1.
American journal of medical genetics. Part A 2003;117A(1):47-56.
2001: Hoover-Fong J E; Geraghty M T; Raymond G V; Thomas G H
Gabapentin interference with urine histidine as measured by the Beckman amino acid analyser.
Journal of inherited metabolic disease 2001;24(3):415-6.

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Julie Hoover-Fong

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