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Showing results 1 to 14 of 14

	Title	Author(s)	Issue Date
	Assessment of linkage and association of 13 genetic loci with bone mineral density Journal:Journal of Bone and Mineral Metabolism	Lau, HHL Ng, MYM Cheung, WMW Paterson, AD Sham, PC Luk, KDK Chan, V Kung, AWC	2006
	Association of low bone mineral density to microsatellite marker on chromosome 16 in Southern Chinese families Proceeding/Conference:International Meeting on the Genetic Epidemiology of Complex Traits	Kung, AWC Ng, MYM Lau, HL Paterson, AD Bulman, D Luk, KDK Chan, VNY	2004
	Clinical and genetic study of a large Italian family linked to SPG12 locus Journal:Neurology	Orlacchio, A Kawarai, T Rogaeva, E Song, Y Paterson, AD Bernardi, G St George-Hyslop, PH	2002
	Disease gene discovery for Familial IgA Nephropathy (FIgAN) by Whole Exome Sequencing (WES) Proceeding/Conference:Journal of the American Society of Nephrology	Song, X Roslin, NM Xu, MY Wang, K Liu, J Joarder, B Haghighi, A Ren, M Li, M Man, C Leung, JCK Tang, SCW Lai, KN Paterson, AD Soubrier, F Pei, YP	2015
	Effect of environmental factors and gender on the heritability of bone mineral density and bone size Journal:Annals of Human Genetics	Ng, MYM Sham, PC Paterson, AD Chan, V Kung, AWC	2006
	A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13 Journal:Clinical Genetics	Zaidi, SHE Peltekova, V Meyer, S Lindinger, A Paterson, AD Tsui, LC FaiyazUlHaque, M Teebi, AS	2005
	Functional impact of global rare copy number variation in autism spectrum disorders Journal: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, C	2010
	Identification of LTBP2 on chromosome 14q as a novel candidate gene for BMD variation and fracture risk association Proceeding/Conference:HKSEMR 2007 Annual Scientific Meeting	Cheung, CL Sham, PC Chan, VNY Paterson, AD Luk, KDK Kung, AWC	2007
	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	Cheung, CL Sham, PC Chan, V Paterson, AD Luk, KDK Kung, AWC	2008
	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	Lo, B FaiyazUlHaque, M Banwell, B Blaser, S Paterson, AD Tsui, LC Teebi, AS	2004
	Low frequency of TAU mutations and further genetic heterogeneity in FTD Proceeding/Conference:International Conference on Alzheimer's Disease & Related Disorders	Kawarai, T Rogaeva, E Song, YQ 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, P	2002
	A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1 Journal:Journal of Investigative Dermatology	Rafiq, MA FaiyazulHaque, M Ud Din, MA Malik, S Sohail, M Anwar, M Haque, S Paterson, AD Tsui, LC Ahmad, W	2005
	Test of linkage and/or association of genes and bone mineral density in Chinese Proceeding/Conference:Journal of Bone and Mineral Research	Kung, AWC Lau, HL Paterson, AD Cheung, WMW Luk, KDK Chan, VNY	2004
	Whole Exome Sequencing (WES) revealed underlying complexity in genetic studies of Familial IgA Nephropathy (flgAN) Proceeding/Conference:Journal of the American Society of Nephrology	Song, X Roslin, NM Xu, MY Wang, K Liu, J Joarder, B Haghighi, A Ren, M Li, M Man, C Leung, JCK Tang, SCW Lai, KN Paterson, AD Soubrier, F Pei, YP	2015

Showing results 1 to 14 of 14