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Title	Author(s)	Issue Date
Characterization of the segmental duplication LCR7-20 in the human genome Journal:Genomics	Liu, X Li, X Li, M Acimovic, YJ Li, Z Scherer, SW Estivill, X Tsui, LC	2004
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development Journal:Human Molecular Genetics	Crackower, MA Scherer, SW Rommens, JM Hui, CC Poorkaj, P Soder, S Cobben, JM Hudgins, L Evans, JP Tsui, LC	1996
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome Journal:Human Molecular Genetics	Estivill, X Cheung, J Pujana, MA Nakabayashi, K Scherer, SW Tsui, LC	2002
Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human Journal:Journal of Biological Chemistry	Rowles, J Scherer, SW Xi, T Majer, M Nickle, DC Rommens, JM Popov, KM Harris, RA Riebow, NL Xia, J Tsui, LC Bogardus, C Prochazka, M	1996
Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5q14 Journal:Mammalian Genome	Crackower, MA Scherer, SW Heng, HHQ Tsui, LC	1997
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

Showing results 12 to 31 of 110 < previous next >