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Author Details
Full Name
Melissa Parkin
Affiliation
The Broad Institute of MIT and Harvard
ORCID
Career Start Year
2007
Papers
22
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
24509480
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Nat Genet
2014
24509480
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Nat Genet
2014
22889921
Genome-wide association study of obsessive-compulsive disorder.
Mol Psychiatry
2013
22889924
Genome-wide association study of Tourette's syndrome.
Mol Psychiatry
2013
22889921
Genome-wide association study of obsessive-compulsive disorder.
Mol Psychiatry
2013
23770567
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Nature
2013
23396133
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Nat Genet
2013
23770567
Mutational heterogeneity in cancer and the search for new cancer-associated genes.
Nature
2013
23396133
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Nat Genet
2013
22889924
Genome-wide association study of Tourette's syndrome.
Mol Psychiatry
2013
22622578
Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature
2012
22885922
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.
Nat Genet
2012
22876189
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet
2012
22622578
Melanoma genome sequencing reveals frequent PREX2 mutations.
Nature
2012
22722202
Sequence analysis of mutations and translocations across breast cancer subtypes.
Nature
2012
22722202
Sequence analysis of mutations and translocations across breast cancer subtypes.
Nature
2012
22885922
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.
Nat Genet
2012
22876189
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet
2012
21307934
The genomic complexity of primary human prostate cancer.
Nature
2011
21307934
The genomic complexity of primary human prostate cancer.
Nature
2011
21892161
Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion.
Nat Genet
2011
21798893
The mutational landscape of head and neck squamous cell carcinoma.
Science
2011
21798893
The mutational landscape of head and neck squamous cell carcinoma.
Science
2011
21892161
Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion.
Nat Genet
2011
20520743
Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples.
Biomark Insights
2010
20933357
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
J Am Coll Cardiol
2010
20811451
Integrating common and rare genetic variation in diverse human populations.
Nature
2010
20520743
Feasibility of High-Throughput Genome-Wide Genotyping using DNA from Stored Buccal Cell Samples.
Biomark Insights
2010
20811451
Integrating common and rare genetic variation in diverse human populations.
Nature
2010
20933357
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
J Am Coll Cardiol
2010
19198609
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Nat Genet
2009
19198609
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Nat Genet
2009
18776908
Integrated detection and population-genetic analysis of SNPs and copy number variation.
Nat Genet
2008
19165918
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
Nat Genet
2008
18776908
Integrated detection and population-genetic analysis of SNPs and copy number variation.
Nat Genet
2008
19165918
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
Nat Genet
2008
17463246
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Science
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
17982456
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.
Nat Genet
2007
17982456
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.
Nat Genet
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17463246
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Science
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
1 - 44 of 44
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Co-authored papers
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Robert C Onofrio
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Co-authored papers
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Wendy Winckler
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Noel Burtt
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Kristian Cibulskis
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Matthew Meyerson
Broad Institute
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6
Kristin G Ardlie
Co-authored papers
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Michael S Lawrence
Co-authored papers
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Benjamin F Voight
Perelman School of Medicine, University of Pennsylvania
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Paul I W de Bakker
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Andrey Sivachenko
Cystic Fibrosis Foundation
Co-authored papers
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Gad Getz
Broad Institute of the Massachusetts Institute of Technology and Harvard
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Levi A Garraway
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