Publications by authors named "Michael Murtha"

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North Asian population relationships in a global context.
Kenneth K Kidd, Baigalmaa Evsanaa, Ariunaa Togtokh, Jane E Brissenden, Janet M Roscoe, Michael Murtha

Sci Rep· May 2022

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The population genetics characteristics of a 90 locus panel of microhaplotypes.
Andrew J Pakstis, Neeru Gandotra, William C Speed, Michael Murtha, Curt Scharfe

Hum Genet· December 2021

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Genetic relationships of Southwest Asian and Mediterranean populations.
Kenneth K Kidd, Ozlem Bulbul, Cemal Gurkan, Mustafa Dogan, Serkan Dogan, Michael Murtha

Forensic Sci Int Genet· July 2021

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, Michael T Murtha

Neuron· September 2015

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A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Pauline Chaste, Lambertus Klei, Stephan J Sanders, Vanessa Hus, Michael T Murtha

Biol Psychiatry· May 2015

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No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.
John D Murdoch, Abha R Gupta, Stephan J Sanders, Michael F Walker, John Keaney, Michael T Murtha

PLoS Genet· January 2015

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The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Michael T Murtha

Nature· November 2014

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Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
Pauline Chaste, Stephan J Sanders, Kommu N Mohan, Lambertus Klei, Youeun Song, Michael T Murtha

Autism Res· June 2014

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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
A Jeremy Willsey, Stephan J Sanders, Mingfeng Li, Shan Dong, Andrew T Tebbenkamp, Michael T Murtha

Cell· November 2013

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Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait.
Pauline Chaste, Lambertus Klei, Stephan J Sanders, Michael T Murtha, Vanessa Hus

Biol Psychiatry· October 2013

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

Nat Genet· September 2013

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Intellectual disability is associated with increased runs of homozygosity in simplex autism.
Ece D Gamsiz, Emma W Viscidi, Abbie M Frederick, Shailender Nagpal, Stephan J Sanders, Michael T Murtha

Am J Hum Genet· July 2013

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Common genetic variants, acting additively, are a major source of risk for autism.
Lambertus Klei, Stephan J Sanders, Michael T Murtha, Vanessa Hus, Jennifer K Lowe

Mol Autism· October 2012

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, Ryan C Murtha

Nature· April 2012

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Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
Patricia B S Celestino-Soper, Chad A Shaw, Stephan J Sanders, Jian Li, Michael T Murtha

Hum Mol Genet· November 2011

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Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha

Neuron· June 2011

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Common variants at five new loci associated with early-onset inflammatory bowel disease.
Marcin Imielinski, Robert N Baldassano, Anne Griffiths, Richard K Russell, Vito Annese, Michael T Murtha

Nat Genet· December 2009

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Applications of protein arrays for small molecule drug discovery and characterization.
Gregory A Michaud, Michael Salcius, Fang Zhou, Vladimir V Papov, Janie Merkel, Michael Murtha

Biotechnol Genet Eng Rev· August 2008

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
Jeffrey C Barrett, Sarah Hansoul, Dan L Nicolae, Judy H Cho, Richard H Duerr, Michael T Murtha

Nat Genet· August 2008

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