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A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease

Human molecular genetics, 2011-01, Vol.20 (2), p.211-222

2011

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Impact of Precision Medicine in Oncology

The cancer journal (Sudbury, Mass.), 2023-01, Vol.29 (1), p.1-2

Kucherlapati, Raju

2023

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Examining transcriptional changes to DNA replication and repair factors over uveal melanoma subtypes

BMC cancer, 2018-08, Vol.18 (1), p.818-818, Article 818

Kucherlapati, Melanie

2018

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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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Co-expression patterns explain how a basic transcriptional role for MYC modulates Wnt and MAPK pathways in colon and lung adenocarcinomas

Cell cycle (Georgetown, Tex.), 2022-08, Vol.21 (15), p.1619-1638

Kucherlapati, Melanie Haas

2022

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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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Oliver Smithies (1925–2017)

Nature (London), 2017-02, Vol.542 (7640), p.166-166

Kucherlapati, Raju

2017

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A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

Nature medicine, 2000-09, Vol.6 (9), p.991-997

2000

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An Msh2 Conditional Knockout Mouse for Studying Intestinal Cancer and Testing Anticancer Agents

Gastroenterology (New York, N.Y. 1943), 2010-03, Vol.138 (3), p.993-1002.e1

2010

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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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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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Mouse models in colon cancer, inferences, and implications

iScience, 2023-06, Vol.26 (6), p.106958-106958, Article 106958

Kucherlapati, Melanie Haas

2023

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Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

Bioinformatics, 2005-10, Vol.21 (19), p.3763-3770

2005

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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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Cardiovascular disease in Noonan syndrome

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

2014

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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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Modulation of proliferation factors in lung adenocarcinoma with an analysis of the transcriptional consequences of genomic EGFR activation

Oncotarget, 2019-12, Vol.10 (65), p.6913-6933

Kucherlapati, Melanie Haas

2019

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Haploinsufficiency of Flap Endonuclease (Fen1) Leads to Rapid Tumor Progression

Proceedings of the National Academy of Sciences - PNAS, 2002-07, Vol.99 (15), p.9924-9929

2002

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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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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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An EGFR targeted PET imaging probe for the detection of colonic adenocarcinomas in the setting of colitis

Theranostics, 2014-01, Vol.4 (9), p.893-903

2014

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Adenomatous polyposis coli (APC) is required for normal development of skin and thymus

PLoS genetics, 2006-09, Vol.2 (9), p.e146-e146

2006

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A novel mouse model of cerebral cavernous malformations based on the two-hit mutation hypothesis recapitulates the human disease

Impact of Precision Medicine in Oncology

Examining transcriptional changes to DNA replication and repair factors over uveal melanoma subtypes

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

Co-expression patterns explain how a basic transcriptional role for MYC modulates Wnt and MAPK pathways in colon and lung adenocarcinomas

Genotype directed therapy in murine mismatch repair deficient tumors

Oliver Smithies (1925–2017)

A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains

An Msh2 Conditional Knockout Mouse for Studying Intestinal Cancer and Testing Anticancer Agents

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

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

Mouse models in colon cancer, inferences, and implications

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

Impaired lymphatic contraction associated with immunosuppression

Cardiovascular disease in Noonan syndrome

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

Modulation of proliferation factors in lung adenocarcinoma with an analysis of the transcriptional consequences of genomic EGFR activation

Haploinsufficiency of Flap Endonuclease (Fen1) Leads to Rapid Tumor Progression

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

Landscape of Somatic Retrotransposition in Human Cancers

A restricted spectrum of NRAS mutations causes Noonan syndrome

Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes

An EGFR targeted PET imaging probe for the detection of colonic adenocarcinomas in the setting of colitis

Adenomatous polyposis coli (APC) is required for normal development of skin and thymus

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