Results 1 to 12 of 12
Page 1 of 1
TypeTitleAuthor(s)YearViews
Functional impact of global rare copy number variation in autism spectrum disorders
Journal:
Nature
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.nature.com/nature
Pinto, D; Pagnamenta, AT; Klei, L; Anney, R; Merico, D; Regan, R; Conroy, J; Magalhaes, TR; Correia, C; Abrahams, BS; Almeida, J; Bacchelli, E; Bader, GD; Bailey, AJ; Baird, G; Battaglia, A; Berney, T; Bolshakova, N; Bölte, S; Bolton, PF; Bourgeron, T; Brennan, S; Brian, J; Bryson, SE; Carson, AR; Casallo, G; Casey, J; Chung, BHY; Cochrane, L; Corsello, C; Crawford, EL; Crossett, A; Cytrynbaum, C; Dawson, G; De Jonge, M; Delorme, R; Drmic, I; Duketis, E; Duque, F; Estes, A; Farrar, P; Fernandez, BA; Folstein, SE; Fombonne, E; Freitag, CM; Gilbert, J; Gillberg, C; Glessner, JT; Goldberg, J; Green, A; Green, J; Guter, SJ; Hakonarson, H; Heron, EA; Hill, M; Holt, R; Howe, JL; Hughes, G; Hus, V; Igliozzi, R; Kim, C; Klauck, SM; Kolevzon, A; Korvatska, O; Kustanovich, V; Lajonchere, CM; Lamb, JA; Laskawiec, M; Leboyer, M; Le Couteur, A; Leventhal, BL; Lionel, AC; Liu, XQ; Lord, C; Lotspeich, L; Lund, SC; Maestrini, E; Mahoney, W; Mantoulan, C; Marshall, CR; Mcconachie, H; Mcdougle, CJ; Mcgrath, J; Mcmahon, WM; Merikangas, A; Migita, O; Minshew, NJ; Mirza, GK; Munson, J; Nelson, SF; Noakes, C; Noor, A; Nygren, G; Oliveira, G; Papanikolaou, K; Parr, JR; Parrini, B; Paton, T; Pickles, A; Pilorge, M; Piven, J; Ponting, CP; Posey, DJ; Poustka, A; Poustka, F; Prasad, A; Ragoussis, J; Renshaw, K; Rickaby, J; Roberts, W; Roeder, K; Roge, B; Rutter, ML; Bierut, LJ; Rice, JP; Salt, J; Sansom, K; Sato, D; Segurado, R; Sequeira, AF; Senman, L; Shah, N; Sheffield, VC; Soorya, L; Sousa, I; Stein, O; Sykes, N; Stoppioni, V; Strawbridge, C; Tancredi, R; Tansey, K; Thiruvahindrapduram, B; Thompson, AP; Thomson, S; Tryfon, A; Tsiantis, J; Van Engeland, H; Vincent, JB; Volkmar, F; Wallace, S; Wang, K; Wang, Z; Wassink, TH; Webber, C; Weksberg, R; Wing, K; Wittemeyer, K; Wood, S; Wu, J; Yaspan, BL; Zurawiecki, D; Zwaigenbaum, L; Buxbaum, JD; Cantor, RM; Cook, EH; Coon, H; Cuccaro, ML; Devlin, B; Ennis, S; Gallagher, L; Geschwind, DH; Gill, M; Haines, JL; Hallmayer, J; Miller, J; Monaco, AP; Nurnberger Jr, JI; Paterson, AD; PericakVance, MA; Schellenberg, GD; Szatmari, P; Vicente, AM; Vieland, VJ; Wijsman, EM; Scherer, SW; Sutcliffe, JS; Betancur, C2010232
 
Identification of LTBP2 on chromosome 14q as a novel candidate gene for bone mineral density variation and fracture risk association
Journal:
Journal of Clinical Endocrinology and Metabolism
Publisher:
The Endocrine Society. The Journal's web site is located at http://jcem.endojournals.org
Cheung, CL; Sham, PC; Chan, V; Paterson, AD; Luk, KDK; Kung, AWC2008120
 
Identification of LTBP2 on chromosome 14q as a novel candidate gene for BMD variation and fracture risk association
Proceedings/Conference:
Hong Kong Society of Endocrinology, Metabolism and Reproduction Annual Scientific Meeting, Hong Kong
Cheung, CL; Sham, PC; Chan, VNY; Paterson, AD; Luk, KDK; Kung, AWC200787
 
Effect of environmental factors and gender on the heritability of bone mineral density and bone size
Journal:
Annals of Human Genetics
Publisher:
Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/AHG
Ng, MYM; Sham, PC; Paterson, AD; Chan, V; Kung, AWC2006160
 
Assessment of linkage and association of 13 genetic loci with bone mineral density
Journal:
Journal of Bone and Mineral Metabolism
Publisher:
Springer Japan. The Journal's web site is located at http://link.springer.de/link/service/journals/00774/index.htm
Lau, HHL; Ng, MYM; Cheung, WMW; Paterson, AD; Sham, PC; Luk, KDK; Chan, V; Kung, AWC2006162
 
A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13
Journal:
Clinical Genetics
Publisher:
Blackwell Munksgaard. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CGE
Zaidi, SHE; Peltekova, V; Meyer, S; Lindinger, A; Paterson, AD; Tsui, LC; FaiyazUlHaque, M; Teebi, AS2005619
 
A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1
Journal:
Journal of Investigative Dermatology
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.nature.com/jid/index.html
Rafiq, MA; FaiyazulHaque, M; Ud Din, MA; Malik, S; Sohail, M; Anwar, M; Haque, S; Paterson, AD; Tsui, LC; Ahmad, W20051,701
 
Association of low bone mineral density to microsatellite marker on chromosome 16 in Southern Chinese families
Proceedings/Conference:
4th International Meeting on the Genetic Epidemiology of complex Traits, 4-7 April 2004, Churchill College, Cambridge, UK
Kung, AWC; Ng, MYM; Lau, HL; Paterson, AD; Bulman, D; Luk, KDK; Chan, VNY2004132
 
The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23
Journal:
Clinical Genetics
Publisher:
Blackwell Munksgaard. The Journal's web site is located at http://www.blackwellpublishing.com/journals/CGE
Lo, B; FaiyazUlHaque, M; Banwell, B; Blaser, S; Paterson, AD; Tsui, LC; Teebi, AS2004658
 
Test of linkage and/or association of genes and bone mineral density in Chinese
Proceedings/Conference:
26th Annual Meeting of the American Society for Bone & Mineral Research, October 1-5, 2004, Seattle, USA. Journal of Bone and Mineral Research
Kung, AWC; Lau, HL; Paterson, AD; Cheung, WMW; Luk, KDK; Chan, VNY200496
 
Clinical and genetic study of a large Italian family linked to SPG12 locus
Journal:
Neurology
Publisher:
Lippincott Williams & Wilkins. The Journal's web site is located at http://www.neurology.org
Orlacchio, A; Kawarai, T; Rogaeva, E; Song, Y; Paterson, AD; Bernardi, G; St George-Hyslop, PH2002107
 
Low frequency of TAU mutations and further genetic heterogeneity in FTD
Proceedings/Conference:
8th International Conference on Alzheimer's Disease and Related Disorders. 20-25 July 2002 Stockholm, Sweden
Kawarai, T; Rogaeva, E; Song, Y; Moliaka, Y; Medeiros, H; Liang, Y; Sato, C; Ling, S; Fong, M; Kolesnikova, T; Bergeron, C; Lang, AE; Paterson, AD; Orlacchio, A; Bernardi, G; Rockwood, K; Allegri, R; Rainero, I; Pinessi, L; Cappa, G; Kertesz, A; Bruni, AC; Freedman, M; Ahern, GL; Tuite, P; Fornazzari, L; St George-Hyslop, P2002121
 
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