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Francis H. Ruddle (1929-2013): A Pioneer in Human Gene Mapping

Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (24), p.9619-9620

Kucherlapati, Raju

2013

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Impaired lymphatic contraction associated with immunosuppression

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.18784-18789

2011

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Landscape of Somatic Retrotransposition in Human Cancers

Science (American Association for the Advancement of Science), 2012-08, Vol.337 (6097), p.967-971

2012

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Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes

Cell, 2013-05, Vol.153 (4), p.919-929

2013

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Clinical significance of CTNNB1 mutation and Wnt pathway activation in endometrioid endometrial carcinoma

JNCI : Journal of the National Cancer Institute, 2014-09, Vol.106 (9), p.1

2014

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Genetically Modified Mouse Models for Biomarker Discovery and Preclinical Drug Testing

Clinical cancer research, 2012-02, Vol.18 (3), p.625-630

KUCHERLAPATI, Raju

2012

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Germline gain-of-function mutations in SOS1 cause Noonan syndrome

Nature genetics, 2007-01, Vol.39 (1), p.70-74

2007

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Cardiovascular disease in Noonan syndrome

Archives of disease in childhood, 2014-07, Vol.99 (7), p.629-634

2014

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Spectrum of somatic mitochondrial mutations in five cancers

Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (35), p.14087-14091

2012

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Global impact of somatic structural variation on the DNA methylome of human cancers

Genome Biology, 2019-10, Vol.20 (1), p.209-209, Article 209

2019

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A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases

Cell reports (Cambridge), 2018-07, Vol.24 (2), p.515-527

2018

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An enhanced genetic model of colorectal cancer progression history

Genome Biology, 2019-08, Vol.20 (1), p.168-168, Article 168

2019

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Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13), p.3502-3512

2017

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Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model

Human molecular genetics, 2011-12, Vol.20 (24), p.4775-4785

2011

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Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Nature genetics, 2001-12, Vol.29 (4), p.465-468

2001

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Next-generation sequencing identifies rare variants associated with Noonan syndrome

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (31), p.11473-11478

2014

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In vivo wide-area cellular imaging by side-view endomicroscopy

Nature methods, 2010-04, Vol.7 (4), p.303

2010

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Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome

American journal of medical genetics. Part A, 2012-12, Vol.158A (12), p.3106-3111

2012

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Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia

Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (50), p.19942-19947

2007

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Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.E1128-E1136

2011

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Impact of Precision Medicine in Oncology

The cancer journal (Sudbury, Mass.), 2023-01, Vol.29 (1), p.1

Kucherlapati, Raju

2023

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Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

The New England journal of medicine, 2008-05, Vol.358 (18), p.1899-1908

2008

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Genotype directed therapy in murine mismatch repair deficient tumors

PloS one, 2013-07, Vol.8 (7), p.e68817

2013

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Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice

PloS one, 2012-09, Vol.7 (9), p.e44273

2012

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Francis H. Ruddle (1929-2013): A Pioneer in Human Gene Mapping

Impaired lymphatic contraction associated with immunosuppression

Landscape of Somatic Retrotransposition in Human Cancers

Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes

Clinical significance of CTNNB1 mutation and Wnt pathway activation in endometrioid endometrial carcinoma

Genetically Modified Mouse Models for Biomarker Discovery and Preclinical Drug Testing

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

Cardiovascular disease in Noonan syndrome

A restricted spectrum of NRAS mutations causes Noonan syndrome

Spectrum of somatic mitochondrial mutations in five cancers

Global impact of somatic structural variation on the DNA methylome of human cancers

A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases

An enhanced genetic model of colorectal cancer progression history

Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model

Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

Next-generation sequencing identifies rare variants associated with Noonan syndrome

In vivo wide-area cellular imaging by side-view endomicroscopy

Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome

Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Impact of Precision Medicine in Oncology

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

Genotype directed therapy in murine mismatch repair deficient tumors

Msh2 acts in medium-spiny striatal neurons as an enhancer of CAG instability and mutant huntingtin phenotypes in Huntington's disease knock-in mice

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