The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35NAKABAYASHI, Kazuhiko; SCHERER, Stephen W.Genomics (San Diego, Calif.). 2001, Vol 73, Num 1, pp 108-112, issn 0888-7543Article

Genomics and pediatric researchBORIGHT, Andrew P; KERE, Juha; SCHERER, Stephen W et al.Pediatric research. 2003, Vol 53, Num 1, pp 4-9, issn 0031-3998, 6 p.Article

Copy-number variations associated with neuropsychiatric conditions : Neuropsychiatric diseaseCOOK, Edwin H; SCHERER, Stephen W.Nature (London). 2008, Vol 455, Num 7215, pp 919-923, issn 0028-0836, 5 p.Article

Structural variation in the human genomeFEUK, Lars; CARSON, Andrew R; SCHERER, Stephen W et al.Nature reviews. Genetics (Print). 2006, Vol 7, Num 2, pp 85-97, issn 1471-0056, 13 p.Article

Human chromosome 7 circa 2004: a model for structural and functional studies of the human genomeSCHERER, Stephen W; GREEN, Eric D.Human molecular genetics (Print). 2004, Vol 13, pp R303-R313, issn 0964-6906, NS2Article

Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 regionKWASNICKA-CRAWFORD, Dorota A; ROBERTS, Wendy; SCHERER, Stephen W et al.Journal of autism and developmental disorders. 2007, Vol 37, Num 4, pp 694-702, issn 0162-3257, 9 p.Article

Copy-number variation in control population cohortsPINTO, Dalila; MARSHALL, Christian; FEUK, Lars et al.Human molecular genetics (Print). 2007, Vol 16, issn 0964-6906, R168-R173, NS2Article

Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD Is it that simple?ANDRADE, Danielle M; SCHERER, Stephen W; MINASSIAN, Berge A et al.Epilepsy research. 2006, Vol 72, Num 1, pp 75-79, issn 0920-1211, 5 p.Article

Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and DiseaseBASSETT, Anne S; SCHERER, Stephen W; BRZUSTOWICZ, Linda M et al.The American journal of psychiatry. 2010, Vol 167, Num 8, pp 899-914, issn 0002-953X, 16 p.Article

GATA1 mutations in transient leukemia and acute megakaryoblastic leukemia of Down syndromeHITZLER, Johann K; CHEUNG, Joseph; YUE LI et al.Blood. 2003, Vol 101, Num 11, pp 4301-4304, issn 0006-4971, 4 p.Article

Mutation analysis of the origin recognition complex subunit 5 (ORC5L) gene in adult patients with myeloid leukemias exhibiting deletions of chromosome band 7q22FRÖHLING, Stefan; NAKABAYASHI, Kazuhiko; SCHERER, Stephen W et al.Human genetics. 2001, Vol 108, Num 4, pp 304-309, issn 0340-6717Article

Localization of the human mGluR4 gene within an epilepsy susceptibility locusWONG, C. Guin-Ting; SCHERER, Stephen W; SNEAD, O. Carter et al.Molecular brain research. 2001, Vol 87, Num 1, pp 109-116, issn 0169-328XArticle

Cloning and characterization of human CADPS and CADPS2, new members of the Ca²⁺-dependent activator for secretion protein familyCISTERAS, Felipe A; VINCENT, John B; SCHERER, Stephen W et al.Genomics (San Diego, Calif.). 2003, Vol 81, Num 3, pp 279-291, issn 0888-7543, 13 p.Article

Identification of a novel protein interacting with laforin, the EPM2A progressive myoclonus epilepsy gene productIANZANO, Leonarda; ZHAO, Xiao C; MINASSIAN, Berge A et al.Genomics (San Diego, Calif.). 2003, Vol 81, Num 6, pp 579-587, issn 0888-7543, 9 p.Article

Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangementsARMENGOL, Lluis; PUJANA, Miguel Angel; CHEUNG, Joseph et al.Human molecular genetics (Print). 2003, Vol 12, Num 17, pp 2201-2208, issn 0964-6906, 8 p.Article

Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNAHANNULA, Katariina; LIPSANEN-NYMAN, Marita; SCHERER, Stephen W et al.Genomics (San Diego, Calif.). 2001, Vol 73, Num 1, pp 1-9, issn 0888-7543Article

Risk factors for autism: translating genomic discoveries into diagnosticsSCHERER, Stephen W; DAWSON, Geraldine.Human genetics. 2011, Vol 130, Num 1, pp 123-148, issn 0340-6717, 26 p.Article

Frequent appearance of novel protein-coding sequences by frameshift translationOKAMURA, Kohji; FEUK, Lars; MARQUES-BONET, Tomas et al.Genomics (San Diego, Calif.). 2006, Vol 88, Num 6, pp 690-697, issn 0888-7543, 8 p.Article

Clonal selection drives genetic divergence of metastatic medulloblastomaXIAOCHONG WU; NORTHCOTT, Paul A; GARZIA, Livia et al.Nature (London). 2012, Vol 482, Num 7386, pp 529-533, issn 0028-0836, 5 p.Article

Early-onset Lafora body diseaseTURNBULL, Julie; GIRARD, Jean-Marie; TYAGI, Atul et al.Brain. 2012, Vol 135, pp 2684-2698, issn 0006-8950, 15 p., 9Article

The Common Inversion of the Williams-Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical SymptomsTAM, Elaine; YOUNG, Edwin J; MORRIS, Colleen A et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 14, pp 1797-1806, issn 1552-4825, 10 p.Article

Sequence variants within exon 1 of MECP2 occur in females with mental retardationHARVEY, Chris G; MENON, Sailesh D; KENNEDY, James L et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 3, pp 355-360, issn 1552-4841, 6 p.Article

Altered expression and deletion of RMO1 in osteosarcomaEPPERT, Kolja; WUNDER, Jay S; ANELIUNAS, Vicky et al.International journal of cancer. 2005, Vol 114, Num 5, pp 738-746, issn 0020-7136, 9 p.Article

Expanded repeat in canine epilepsyLOHI, Hannes; YOUNG, Edwin J; SUTTER, Nathan B et al.Science (Washington, D.C.). 2005, Vol 307, Num 5706, issn 0036-8075, p. 81Article

Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delayKWASNICKA-CRAWFORD, Dorota A; CARSON, Andrew R; ROBERTS, Wendy et al.Genomics (San Diego, Calif.). 2005, Vol 86, Num 2, pp 182-194, issn 0888-7543, 13 p.Article