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MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia

Nature genetics, 2002-01, Vol.30 (1), p.41-47

2002

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

Nature genetics, 1999-07, Vol.22 (3), p.231-238

1999

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Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

Nature genetics, 2012-06, Vol.44 (6), p.685-689

2012

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Efficient mapping of mendelian traits in dogs through genome-wide association

Nature genetics, 2007-11, Vol.39 (11), p.1321-1328

2007

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Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy

Nature genetics, 2010-08, Vol.42 (8), p.715-721

2010

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The Cancer Genome Atlas Pan-Cancer analysis project

Nature genetics, 2013-10, Vol.45 (10), p.1113-1120

2013

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Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays

Nature genetics, 1999-06, Vol.22 (2), p.164-167

1999

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PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Nature genetics, 2003-07, Vol.34 (3), p.267-273

2003

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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature genetics, 2013-03, Vol.45 (3), p.299-303

2013

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Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

Nature genetics, 1997-09, Vol.17 (1), p.88-91

1997

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The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

Nature genetics, 2000-09, Vol.26 (1), p.76-80

2000

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Variation in genome-wide mutation rates within and between human families

Nature genetics, 2011-07, Vol.43 (7), p.712-714

2011

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Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

Nature genetics, 1996-01, Vol.12 (1), p.100-102

1996

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Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation

Nature genetics, 2001-01, Vol.27 (1), p.31-39

2001

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New models of collaboration in genome-wide association studies: the Genetic Association Information Network

Nature genetics, 2007-09, Vol.39 (9), p.1045-1051

2007

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A genetic map of the mouse with 4,006 simple sequence length polymorphisms

Nature genetics, 1994-06, Vol.7 (2S), p.220-245

1994

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A radiation hybrid map of mouse genes

Nature genetics, 2001-10, Vol.29 (2), p.201-205

2001

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Genomic analysis of primary tumors does not address the prevalence of metastatic cells in the population

Nature genetics, 2003-05, Vol.34 (1), p.23-23

2003

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

Nature genetics, 1999-11, Vol.23 (3), p.373-373

Cargill, Michele

1999

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The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

Nature genetics, 2000-09, Vol.26 (1), p.76-80

2000

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A genetic map of the mouse with 4,006 simple sequence length polymorphisms

Nature genetics, 1994, Vol.7 (JUN), p.220-245

1994

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MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia

Genomic analysis identifies targets of convergent positive selection in drug-resistant Mycobacterium tuberculosis

Characterization of single-nucleotide polymorphisms in coding regions of human genes

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity

Efficient mapping of mendelian traits in dogs through genome-wide association

Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapy

The Cancer Genome Atlas Pan-Cancer analysis project

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

Variation in genome-wide mutation rates within and between human families

Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation

New models of collaboration in genome-wide association studies: the Genetic Association Information Network

A genetic map of the mouse with 4,006 simple sequence length polymorphisms

A radiation hybrid map of mouse genes

A YAC-based physical map of the mouse genome

Genomic analysis of primary tumors does not address the prevalence of metastatic cells in the population

Characterization of single-nucleotide polymorphisms in coding regions of human genes

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

A genetic map of the mouse with 4,006 simple sequence length polymorphisms

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