Author: Jeffrey C Murray

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Preprints

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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  • Site-wide: 11,902
  • In genetics: 598
• Year to date:
  • Site-wide: 86,532
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  • Site-wide: 89,751

Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

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  • Site-wide: 15,162
  • In genetics: 777
• Year to date:
  • Site-wide: 64,485
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  • Site-wide: 61,602

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

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  • Site-wide: 32,500
  • In genetics: 1,613
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Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

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  • Site-wide: 47,148
  • In genetics: 2,254
• Year to date:
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  • Site-wide: 93,542

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

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  • Site-wide: 49,117
  • In genetics: 2,347
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  • Site-wide: 99,557

Haplotype genetic score analysis in 10,734 mother/infant pairs reveals complex maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes and adult phenotypes

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  • Site-wide: 52,223
  • In genetics: 2,484
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  • Site-wide: 55,491
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  • Site-wide: 54,668

Detection of de novo copy number deletions from targeted sequencing of trios

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  • Site-wide: 59,533
  • In bioinformatics: 5,934
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  • Site-wide: 112,894
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  • Site-wide: 102,800

Coding de novo mutations identified by WGS reveal novel orofacial cleft genes

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  • In genetics: 3,094
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  • Site-wide: 28,586

Genome Wide Interaction Studies Identify Sex-Specific Risk Alleles for Nonsyndromic Orofacial Clefts

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  • Site-wide: 86,858
  • In genetics: 3,993
• Year to date:
  • Site-wide: 100,638
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  • Site-wide: 93,517

Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21

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  • Site-wide: 102,871
  • In genetics: 4,608
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  • Site-wide: 96,588
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Risk of preeclampsia in patients with genetic predisposition to common medical conditions: a case-control study

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  • In genetics: 4,802
• Year to date:
  • Site-wide: 102,535
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The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only

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  • Site-wide: 123,406
  • In genetic and genomic medicine: 570
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  • Site-wide: 77,004
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  • Site-wide: 48,970

Genome-wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions

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  • Site-wide: 126,133
  • In epidemiology: 5,044
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  • Site-wide: 78,421
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  • Site-wide: 86,870