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Reference EntriesFull Text
Kucherlapati, Raju Suryanarayana
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: KNO-LIS, 2022, p.6316-6316
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Kucherlapati, Raju Suryanarayana
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: KNO-LIT, 2021, p.6294-6294
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ArticlesPeer ReviewedFull Text
Francis H. Ruddle (1929-2013): A Pioneer in Human Gene Mapping
Author / Creator:Kucherlapati, Raju
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (24), p.9619-9620
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ArticlesPeer ReviewedFull Text
Impaired lymphatic contraction associated with immunosuppression
Author / Creator:Liao, Shan ; Cheng, Gang ; Conner, David A. ; Huang, Yuhui ; Kucherlapati, Raju S. ; Munn, Lance L. ; Ruddle, Nancy H. ; Jain, Rakesh K. ; Fukumura, Dai ; Padera, Timothy P.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.18784-18789
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ArticlesPeer ReviewedFull Text
Landscape of Somatic Retrotransposition in Human Cancers
Author / Creator:Lee, Eunjung ; Iskow, Rebecca ; Yang, Lixing ; Gokcumen, Omer ; Haseley, Psalm ; Luquette, Lovelace J. ; Lohr, Jens G. ; Harris, Christopher C. ; Ding, Li ; Wilson, Richard K. ; Wheeler, David A. ; Gibbs, Richard A. ; Kucherlapati, Raju ; Lee, Charles ; Kharchenko, Peter V. ; Park, Peter J.
Publisher:Washington, DC: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2012-08, Vol.337 (6097), p.967-971
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ArticlesPeer ReviewedFull Text
Spectrum of somatic mitochondrial mutations in five cancers
Author / Creator:Larman, Tatianna C ; DePalma, Steven R ; Hadjipanayis, Angela G ; Protopopov, Alexei ; Zhang, Jianhua ; Gabriel, Stacey B ; Chin, Lynda ; Seidman, Christine E ; Kucherlapati, Raju ; Seidman, J. G
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (35), p.14087-14091
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ArticlesPeer ReviewedFull Text
Germline gain-of-function mutations in SOS1 cause Noonan syndrome
Author / Creator:Roberts, Amy E ; Araki, Toshiyuki ; Swanson, Kenneth D ; Montgomery, Kate T ; Schiripo, Taryn A ; Joshi, Victoria A ; Li, Li ; Yassin, Yosuf ; Tamburino, Alex M ; Neel, Benjamin G ; Kucherlapati, Raju S
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2007-01, Vol.39 (1), p.70-74
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ArticlesPeer ReviewedFull Text
A restricted spectrum of NRAS mutations causes Noonan syndrome
Author / Creator:Cirstea, Ion C ; Kutsche, Kerstin ; Dvorsky, Radovan ; Gremer, Lothar ; Carta, Claudio ; Horn, Denise ; Roberts, Amy E ; Lepri, Francesca ; Merbitz-Zahradnik, Torsten ; König, Rainer ; Kratz, Christian P ; Pantaleoni, Francesca ; Dentici, Maria L ; Joshi, Victoria A ; Kucherlapati, Raju S ; Mazzanti, Laura ; Mundlos, Stefan ; Patton, Michael A ; Silengo, Margherita Cirillo ; Rossi, Cesare ; Zampino, Giuseppe ; Digilio, Cristina ; Stuppia, Liborio ; Seemanova, Eva ; Pennacchio, Len A ; Gelb, Bruce D ; Dallapiccola, Bruno ; Wittinghofer, Alfred ; Ahmadian, Mohammad R ; Tartaglia, Marco ; Zenker, Martin
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2010-01, Vol.42 (1), p.27-29
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ArticlesPeer ReviewedFull Text
An enhanced genetic model of colorectal cancer progression history
Author / Creator:Yang, Lixing ; Wang, Su ; Lee, Jake June-Koo ; Lee, Semin ; Lee, Eunjung ; Shinbrot, Eve ; Wheeler, David A. ; Kucherlapati, Raju ; Park, Peter J.
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology, 2019-08, Vol.20 (1), p.168-168, Article 168
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ArticlesPeer ReviewedFull Text
Cardiovascular disease in Noonan syndrome
Author / Creator:Prendiville, Terence W ; Gauvreau, Kimberlee ; Tworog-Dube, Erica ; Patkin, Lynne ; Kucherlapati, Raju S ; Roberts, Amy E ; Lacro, Ronald V
Publisher:London: BMJ Publishing Group
Journal title:Archives of disease in childhood, 2014-07, Vol.99 (7), p.629-634
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ArticlesPeer ReviewedFull Text
Next-generation sequencing identifies rare variants associated with Noonan syndrome
Author / Creator:Chen, Peng-Chieh ; Yin, Jiani ; Yu, Hui-Wen ; Yuan, Tao ; Fernande, Minerva ; Yung, Christina K. ; Trinh, Quang M. ; Peltekova, Vanya D. ; Reid, Jeffrey G. ; Tworog-Dube, Erica ; Morgan, Margaret B. ; Muzny, Donna M. ; Stein, Lincoln ; McPherson, John D. ; Roberts, Amy E. ; Gibbs, Richard A. ; Neel, Benjamin G. ; Kucherlapati, Raju
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (31), p.11473-11478
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Newsletter articlesFull Text
Tal Medical, Inc.; Tal Medical Secures $14M Financing Round and Adds Industry Veterans to Team
Publisher:Atlanta: NewsRx
Journal title:Biotech Business Week, 2015, p.111
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ArticlesPeer ReviewedFull Text
Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion
Author / Creator:Xi, Ruibin ; Hadjipanayis, Angela G ; Luquette, Lovelace J ; Kim, Tae-Min ; Lee, Eunjung ; Zhang, Jianhua ; Johnson, Mark D ; Muzny, Donna M ; Wheeler, David A ; Gibbs, Richard A ; Kucherlapati, Raju ; Park, Peter J
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.E1128-E1136
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ArticlesPeer ReviewedFull Text
Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia
Author / Creator:Lencz, Todd ; Lambert, Christophe ; DeRosse, Pamela ; Burdick, Katherine E ; Morgan, T. Vance ; Kane, John M ; Kucherlapati, Raju ; Malhotra, Anil K
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (50), p.19942-19947
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ArticlesPeer ReviewedFull Text
In vivo wide-area cellular imaging by side-view endomicroscopy
Author / Creator:Kim, Pilhan ; Chung, Euiheon ; Yamashita, Hiroshi ; Hung, Kenneth E ; Mizoguchi, Atsushi ; Kucherlapati, Raju ; Fukumura, Dai ; Jain, Rakesh K ; Yun, Seok H
Publisher:New York: Nature Publishing Group US
Journal title:Nature methods, 2010-04, Vol.7 (4), p.303-305
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ArticlesPeer ReviewedFull Text
Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults
Author / Creator:Morita, Hiroyuki ; Rehm, Heidi L ; Menesses, Andres ; McDonough, Barbara ; Roberts, Amy E ; Kucherlapati, Raju ; Towbin, Jeffrey A ; Seidman, J.G ; Seidman, Christine E
Publisher:Boston, MA: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2008-05, Vol.358 (18), p.1899-1908
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ArticlesPeer ReviewedFull Text
Global impact of somatic structural variation on the DNA methylome of human cancers
Author / Creator:Zhang, Yiqun ; Yang, Lixing ; Kucherlapati, Melanie ; Hadjipanayis, Angela ; Pantazi, Angeliki ; Bristow, Christopher A. ; Lee, Eunjung Alice ; Mahadeshwar, Harshad S. ; Tang, Jiabin ; Zhang, Jianhua ; Seth, Sahil ; Lee, Semin ; Ren, Xiaojia ; Song, Xingzhi ; Sun, Huandong ; Seidman, Jonathan ; Luquette, Lovelace J. ; Xi, Ruibin ; Chin, Lynda ; Protopopov, Alexei ; Park, Peter J. ; Kucherlapati, Raju ; Creighton, Chad J.
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology, 2019-10, Vol.20 (1), p.209-209, Article 209
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ArticlesPeer ReviewedFull Text
Development of a Mouse Model for Sporadic and Metastatic Colon Tumors and Its Use in Assessing Drug Treatment
Author / Creator:Hung, Kenneth E. ; Maricevich, Marco A. ; Richard, Larissa Georgeon ; Chen, Wei Y. ; Richardson, Michael P. ; Kunin, Alexandra ; Bronson, Roderick T. ; Mahmood, Umar ; Kucherlapati, Raju ; Kolodner, Richard D.
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2010-01, Vol.107 (4), p.1565-1570
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ArticlesPeer ReviewedFull Text
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
Author / Creator:Tartaglia, Marco ; Mehler, Ernest L. ; Goldberg, Rosalie ; Zampino, Giuseppe ; Brunner, Han G. ; Kremer, Hannie ; van der Burgt, Ineke ; Crosby, Andrew H. ; Ion, Andra ; Jeffery, Steve ; Kalidas, Kamini ; Patton, Michael A. ; Kucherlapati, Raju S. ; Gelb, Bruce D.
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2001-12, Vol.29 (4), p.465-468
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ArticlesPeer ReviewedFull Text
Colorectal Cancer in Mice Genetically Deficient in the Mucin Muc2
Author / Creator:Velcich, Anna ; Yang, WanCai ; Heyer, Joerg ; Fragale, Alessandra ; Nicholas, Courtney ; Viani, Stephanie ; Kucherlapati, Raju ; Lipkin, Martin ; Yang, Kan ; Augenlicht, Leonard
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2002-03, Vol.295 (5560), p.1726-1729
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Kucherlapati, Raju Suryanarayana

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Kucherlapati, Raju Suryanarayana

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

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Impaired lymphatic contraction associated with immunosuppression

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Landscape of Somatic Retrotransposition in Human Cancers

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Spectrum of somatic mitochondrial mutations in five cancers

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

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A restricted spectrum of NRAS mutations causes Noonan syndrome

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An enhanced genetic model of colorectal cancer progression history

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Cardiovascular disease in Noonan syndrome

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Next-generation sequencing identifies rare variants associated with Noonan syndrome

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Tal Medical, Inc.; Tal Medical Secures $14M Financing Round and Adds Industry Veterans to Team

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

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Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia

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

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Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

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

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Development of a Mouse Model for Sporadic and Metastatic Colon Tumors and Its Use in Assessing Drug Treatment

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

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Colorectal Cancer in Mice Genetically Deficient in the Mucin Muc2

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