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Title	Author(s)	Issue Date
Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5 Journal:Nucleic Acids Research	Wilson, MD Riemer, C Martindale, DW Schnupf, P Boright, AP Cheung, TL Hardy, DM Schwartz, S Scherer, SW Tsui, LC Miller, W Koop, BF	2001
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor Journal:Cell	Freund, CL GregoryEvans, CY Furukawa, T Papaioannou, M Looser, J Ploder, L Bellingham, J Ng, D Herbrick, JAS Duncan, A Scherer, SW Tsui, LC LoutradisAnagnostou, A Jacobson, SG Cepko, CL Bhattacharya, SS McInnes, RR	1997
Crosstalk between histone modification and DNA methylation in patients with intellectual disability syndrome due to JARID1C mutations Proceeding/Conference:Canadian Epigenetics Conference, Eh! 2011	Chung, BHY Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Wekserg, R	2011
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Chung, B Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Weksberg, R	2010
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2010	Chung, BHY Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Weksberg, R	2010
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly Journal:Human Genetics	Roessler, E Ward, DE Gaudenz, K Belloni, E Scherer, SW Donnai, D SiegelBartelt, J Tsui, LC Muenke, M	1997
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine	MAK, CCY Chow, PC Liu, APY Chan, YK Chu, WY Mok, TKG LEUNG, KC YEUNG, KS Chau, AKT Lowther, C Scherer, SW Marshall, CR Bassett, AS Chung, BHY	2016
Delineation of genomic regions in chromosome band 7q22 commonly deleted in myeloid leukemias. Journal:Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer	Fischer, K Brown, J Scherer, SW Schramm, P Stewart, J Fugazza, G Pascheberg, U Peter, W Tsui, LC Lichter, P Döhner, H	1998
Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of MET Journal:Oncogene	Lin, JC Scherer, SW Tougas, L Traverso, G Tsui, LC Andrulis, IL Jothy, S Park, M	1996
DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes Journal:The American Journal of Human Genetics	Choufani, S Gibson, WT Turinsky, AL Chung, BHY Wang, T Garg, K Vitriolo, A Cohen, ASA Cyrus, S Goodman, S Chater-Diehl, E Brzezinski, J Brudno, M Luk, HM White, SM Lynch, SA Clericuzio, C Temple, IK Flinter, F MdConnell, V Cushing, T Bird, LM Splitt, M Kerr, B Scherer, SW Machado, J Imagawa, E Okamoto, N Matsumoto, N Testa, G Iascone, M Tenconi, R Caluseriu, O Mendoza-Londono, R Chitayat, D Cytrynabum, C Tatton-Brown, K Weksberg, R	2020
Dysmorphology assessment on a population basesd cohort of 150 newfoundland children with autism spectrum disorder Proceeding/Conference:30th Annual David W. Smith Workshop	Fernandez, BA Turner, L MacKay, S Weksberg, R Chung, BHY Roberts, W Vardy, C Whitten, K Marshal, C Scherer, SW	2009
Dysregulation of cyclin dependent kinase 6 expression in splenic marginal zone lymphoma through chromosome 7q translocations Journal:Oncogene	Corcoran, MM Mould, SJ Orchard, JA Ibbotson, RE Chapman, RM Boright, AP Platt, C Tsui, LC Scherer, SW Oscier, DG	1999
EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome Journal:Journal of Translational Genetics and Genomics	Goodman, SJ Cytrynbaum, C Chung, BHY Chater-Diehl, E Aziz, C Turinsky, AL Kellam, B Keller, M Ko, JM Caluseriu, O Grafodatskaya, D McCready, E Perrier, R Yeung, KS Luk, HM Machado, J Brudno, M Stavropoulos, DJ Scherer, SW Innes, AM Cheung, SW Choufani, S Weksberg, R	2020
Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation Journal:American Journal of Human Genetics	Palmer, SE Scherer, SW Kukolich, M Wijsman, EM Tsui, LC Stephens, K Evans, JP	1994
Exome sequencing of a pedigree with Caudal Regression Syndrome (CRS) Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2012	Cheng, G Wong, EHM Sham, PC Cherny, SS Maas, S Scherer, SW Marshall, CR Pereira, SL Tam, PKH Garcia-Barcelo, MM	2012
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1	Scherer, SW Poorkaj, P Allen, T Kim, J Geshuri, D Nunes, M Soder, S Stephens, K Pagon, RA Patton, MA Berg, MA Donlon, T Rivera, H Pfeiffer, RA Naritomi, K Hughes, H Genuardi, M Gurrieri, F Neri, G Lovrein, E Magenis, E Tsui, L-C Evans, JP	1994
Fine mapping of the human and mouse genes for the type i procollagen COOH-terminal proteinase enhancer protein Journal:Genomics	Takahara, K Osborne, L Elliott, RW Tsui, LC Scherer, SW Greenspan, DS	1996
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6 Journal:Mammalian Genome	Crackower, MA Heng, HHQ Shi, X Scherer, SW Tsui, LC	1997
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
Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia Journal:Nature Genetics	Ma, Z Morris, SW Valentine, V L, M Herbrick, JA Cui, X Bouman, D Li, Y Mehta, PK Nizetic, D Kaneko, Y Chan, GCF Chan, LC Squire, J Scherer, SW Hitzler, JK	2001

Showing results 17 to 36 of 110 < previous next >