Autism and related neurodevelopmental disorders: the many genes involved

por Scherer, Stephen W
Publicado 2014

Genomic medicine goes mainstream

por Scherer, Stephen W
Publicado 2016

The mouse genome sequence - the end of the tail, or just the beginning?

por Rossant, Janet, Scherer, Stephen W
Publicado 2003

Identification of candidate intergenic risk loci in autism spectrum disorder

por Walker, Susan, Scherer, Stephen W
Publicado 2013

Identifying concerted evolution and gene conversion in mammalian gene pairs lasting over 100 million years

por Carson, Andrew R, Scherer, Stephen W
Publicado 2009

Syndromic autism spectrum disorders: moving from a clinically defined to a molecularly defined approach

por Fernandez, Bridget A., Scherer, Stephen W.
Publicado 2017

Evolutionary implications of inversions that have caused intra-strand parity in DNA

por Okamura, Kohji, Wei, John, Scherer, Stephen W
Publicado 2007

Duplication and relocation of the functional DPY19L2 gene within low copy repeats

por Carson, Andrew R, Cheung, Joseph, Scherer, Stephen W
Publicado 2006

Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting

por Okamura, Kohji, Wintle, Richard F, Scherer, Stephen W
Publicado 2008

Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders

por Hoang, Ny, Buchanan, Janet A., Scherer, Stephen W.
Publicado 2018

Discovery of genomic variation across a generation

por Trost, Brett, Loureiro, Livia O, Scherer, Stephen W
Publicado 2021

Building Trust in 21(st) Century Genomics

por Szego, Michael J., Buchanan, Janet A., Scherer, Stephen W.
Publicado 2013

Strategies for the detection of copy number and other structural variants in the human genome

por Carson, Andrew R, Feuk, Lars, Mohammed, Mansoor, Scherer, Stephen W
Publicado 2006

Environmental exposures associated with elevated risk for autism spectrum disorder may augment the burden of deleterious de novo mutations among probands

por Pugsley, Kealan, Scherer, Stephen W., Bellgrove, Mark A., Hawi, Ziarih
Publicado 2021

PI4K2A deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndrome

por Alkhater, Reem A., Scherer, Stephen W., Minassian, Berge A., Walker, Susan
Publicado 2018

Genome sequencing as a diagnostic test

por Costain, Gregory, Cohn, Ronald D., Scherer, Stephen W., Marshall, Christian R.
Publicado 2021

Séquençage du génome comme test diagnostique

por Costain, Gregory, Cohn, Ronald D., Scherer, Stephen W., Marshall, Christian R.
Publicado 2022

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

por Bassett, Anne S., Marshall, Christian R., Lionel, Anath C., Chow, Eva W.C., Scherer, Stephen W.
Publicado 2008

A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV data

por Nishiyama, Takeshi, Takahashi, Kunihiko, Tango, Toshiro, Pinto, Dalila, Scherer, Stephen W, Takami, Satoshi, Kishino, Hirohisa
Publicado 2011

The Database of Genomic Variants: a curated collection of structural variation in the human genome

por MacDonald, Jeffrey R., Ziman, Robert, Yuen, Ryan K. C., Feuk, Lars, Scherer, Stephen W.
Publicado 2014