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M. Murtha · SciRah

Researcher profile · Semantic Scholar

M. Murtha

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M. Murtha — researcher profile on SciRah

h-index: 26
Works: 33
Citations: 16K

Most-cited papers

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
J. Barrett, S. Hansoul, D. Nicolae, Judy H. Cho +57 more
2008Nature Genetics2,726 citations Open access
Semantic Scholar
The contribution of de novo coding mutations to autism spectrum disorder
I. Iossifov, B. O'Roak, Stephan J Sanders, M. Ronemus +43 more
2014Nature2,511 citations Open access
Semantic Scholar
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. H. S. B. M. S. V. S. M. R. H. B. Lee Ripke Neale Faraone Purcell Perlis Mowry Thapa, Hong S. Lee, S. Ripke, B. Neale +367 more
2013Nature Genetics2,210 citations Open access
Semantic Scholar
De novo mutations revealed by whole exome sequencing are strongly associated with autism
Stephan J Sanders, M. Murtha, Abha R. Gupta, John D. Murdoch +26 more
2012Nature2,094 citations Open access
Semantic Scholar
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J Sanders, Xin He, A. Willsey, A. Ercan-Sencicek +42 more
2015Neuron1,424 citations Open access
Semantic Scholar
Multiple recurrent de novo copy number variations (CNVs), including duplications of the 7q11.23 Williams-Beuren syndrome region, are strongly associated with autism
Stephan J Sanders, A. Ercan-Sencicek, Vanessa Hus, Rui Luo +63 more
2011Neuron1,287 citations Open access
Semantic Scholar
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
A. Willsey, Stephan J Sanders, Ming-Feng Li, Shan Dong +31 more
2013Cell925 citations Open access
Semantic Scholar
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm Lizzy Phil H Laramie Neelroop N Stephen Stephan Be O'Dushlaine Rossin Lee Duncan Parikshak Newhouse R, C. O'Dushlaine, L. Rossin, P. Lee +372 more
2015Nature Neuroscience765 citations Open access
Semantic Scholar
Common genetic variants, acting additively, are a major source of risk for autism
L. Klei, Stephan J Sanders, M. Murtha, Vanessa Hus +21 more
2012Molecular Autism410 citations Open access
Semantic Scholar
Surveys of Gene Families Using Polymerase Chain Reaction: PCR Selection and PCR Drift
A. Wagner, N. Blackstone, P. Cartwright, M. H. Dick +6 more
1994292 citations
Semantic Scholar
Evolution of Hox genes.
F. Ruddle, Janet L. Bartels, K. Bentley, C. Kappen +2 more
1994Annual Review of Genetics252 citations
Semantic Scholar
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
R. Maier, G. Moser, Guo-Bo Chen, S. Ripke +373 more
2015American Journal of Human Genetics226 citations Open access
Semantic Scholar
Gene expression analysis by transcript profiling coupled to a gene database query
R. Shimkets, D. Lowe, J. Tai, P. Sehl +16 more
1999Nature Biotechnology196 citations
Semantic Scholar
Expansion of the Hox gene family and the evolution of chordates.
John W. Pendleton, B. K. Nagai, M. Murtha, F. Ruddle
1993Proceedings of the National Academy of Sciences of the United States of America174 citations Open access
Semantic Scholar
Detection of homeobox genes in development and evolution.
M. Murtha, J. Leckman, F. Ruddle
1991Proceedings of the National Academy of Sciences of the United States of America155 citations Open access
Semantic Scholar
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
Patrícia B. S. Celestino-Soper, C. Shaw, Stephan J Sanders, Jian Li +14 more
2011Human Molecular Genetics123 citations Open access
Semantic Scholar
Gene loss and gain in the evolution of the vertebrates.
F. Ruddle, K. Bentley, M. Murtha, N. Risch
1994Development102 citations
Semantic Scholar
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait
P. Chaste, L. Klei, Stephan J Sanders, M. Murtha +20 more
2013Biological Psychiatry82 citations Open access
Semantic Scholar
Expression pattern of a murine homeobox gene, Dbx, displays extreme spatial restriction in embryonic forebrain and spinal cord.
Sang-Wei Lu, L. Bogarad, M. Murtha, F. Ruddle
1992Proceedings of the National Academy of Sciences of the United States of America82 citations Open access
Semantic Scholar
Homeoboxes in cnidarians.
B. Schierwater, M. Murtha, M. H. Dick, F. Ruddle +1 more
1991The Journal of experimental zoology70 citations
Semantic Scholar
Intellectual disability is associated with increased runs of homozygosity in simplex autism.
E. Gamsiz, E. Viscidi, A. M. Frederick, Shailender Nagpal +10 more
2013American Journal of Human Genetics67 citations Open access
Semantic Scholar
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2
P. Chaste, Stephan J Sanders, K. N. Mohan, L. Klei +23 more
2014Autism Research63 citations Open access
Semantic Scholar
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 +16 more
2015PLoS Genetics56 citations Open access
Semantic Scholar
Multiple Hox/HOM-class homeoboxes in Platyhelminthes.
Janet L. Bartels, M. Murtha, Francis H. Ruddle
1993Molecular Phylogenetics and Evolution41 citations Open access
Semantic Scholar
The population genetics characteristics of a 90 locus panel of microhaplotypes
A. Pakstis, Neeru Gandotra, W. C. Speed, M. Murtha +2 more
2021Human Genetics29 citations Open access
Semantic Scholar
Developmental expression of the glucose dehydrogenase gene in Drosophila melanogaster.
Diana L. Cox-Foster, Christopher P. Schonbaum, M. Murtha, D. Cavener
1990Genetics27 citations Open access
Semantic Scholar
Characterization and sequence analysis of the human homeobox-containing gene GBX2.
Xu Lin, Anand Swaroop, Flora M. Vaccarino, M. Murtha +4 more
1996Genomics19 citations Open access
Semantic Scholar
A genomewide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
P. Chaste, L. Klei, Stephan J Sanders, Vanessa Hus +20 more
2014Biological Psychiatry11 citations Open access
Semantic Scholar
Genetic relationships of Southwest Asian and Mediterranean populations.
K. Kidd, O. Bulbul, Cemal Gurkan, M. Doğan +8 more
2021Forensic Science International: Genetics10 citations Open access
Semantic Scholar
North Asian population relationships in a global context
K. Kidd, Baigalmaa Evsanaa, Ariunaa Togtokh, J. Brissenden +10 more
2022Scientific Reports9 citations Open access
Semantic Scholar
The YYRR box: a conserved dipyrimidine-dipurine sequence element in Drosophila and other eukaryotes.
D. Cavener, Yue Feng, Brian D. Foster, P. Krasney +3 more
1988Nucleic Acids Research7 citations Open access
Semantic Scholar
Genetic mapping of a new homeobox gene to mouse chromosome 7.
K. R. Johnson, Sang-Wei Lu, M. Murtha, F. Ruddle +1 more
1992Genomics5 citations
Semantic Scholar
Volume 16 Number 8 1988 Nucleic Acids Research The YYRR box : a conserved dipyrimidine — djpurine sequence element in Drosophila and other eukaryotes
D. Cavener, Yue Feng, B. Foster, P. Krasney +2 more
20050 citations
Semantic Scholar

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