Raju Kucherlapati

发表

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

Peter J. Park, Weil R. Lai, Mark D. Johnson, 2005, Bioinform..

Application of Technology: Internet-based Support for Bioscience Research: A Collaborative Genome center for Human Chromosome 12

Kenneth S. Krauter, Perry L. Miller, Prakash M. Nadkarni, 1995, J. Am. Medical Informatics Assoc..

Predictive Models in Personalized Medicine: Neural Information Processing Systems (NIPS), 2010 workshop report

Rómer Rosales, Shipeng Yu, Jude W. Shavlik, 2011, SIGH.

Initiating oncogenic event determines gene-expression patterns of human breast cancer models

Richard Simon, Nianqing Xiao, Raju Kucherlapati, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Cathepsin B Expression and Survival in Colon Cancer: Implications for Molecular Detection of Neoplasia

Shuji Ogino, Umar Mahmood, Raju Kucherlapati, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia

Todd Lencz, Anil K Malhotra, Raju Kucherlapati, 2007, Proceedings of the National Academy of Sciences.

A gender‐moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo‐cardio‐facial syndrome (22q11.2 deletion syndrome)

Birgit Funke, Wanda Fremont, Nuria Y. AbdulSabur, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood

Peter J. Park, Jennifer J. Lund, Richard L. Maas, 2009, Development.

Genetic variation in DTNBP1 influences general cognitive ability.

Birgit Funke, Todd Lencz, Anil K Malhotra, 2006, Human molecular genetics.

Colorectal Cancer in Mice Genetically Deficient in the Mucin Muc2

Kan Yang, Raju Kucherlapati, R. Kucherlapati, 2002, Science.

(CAG)n-hairpin DNA binds to Msh2–Msh3 and changes properties of mismatch recognition

Raju Kucherlapati, R. Kucherlapati, W. Edelmann, 2005, Nature Structural &Molecular Biology.

Association of the DTNBP1 locus with schizophrenia in a U.S. population.

Birgit Funke, Stephen Lake, Anil K Malhotra, 2004, American journal of human genetics.

Cardiac defects and renal failure in mice with targeted mutations in Pkd2

Lin Geng, Raju Kucherlapati, Li Li, 2000, Nature Genetics.

COMT genetic variation confers risk for psychotic and affective disorders: a case control study

Birgit Funke, Todd Lencz, Anil K Malhotra, 2005, Behavioral and Brain Functions.

Next-generation sequencing identifies rare variants associated with Noonan syndrome

John D McPherson, Richard A Gibbs, Lincoln D. Stein, 2014, Proceedings of the National Academy of Sciences.

TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome

Birgit Funke, James B. Kobler, Peter Scambler, 2001, Cell.

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

Euiheon Chung, Pilhan Kim, Dai Fukumura, 2010, Nature Methods.

A mouse plasma peptide atlas as a resource for disease proteomics

Ruedi Aebersold, Eric W Deutsch, Gilbert S Omenn, 2008, Genome Biology.

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

Sebastiaan Overeem, Emmanuel Mignot, Seiji Nishino, 2000, Nature Medicine.

Meiotic Pachytene Arrest in MLH1-Deficient Mice

Asad Umar, Jeffrey W Pollard, Raju Kucherlapati, 1996, Cell.

Gene Transfer

Raju Kucherlapati, R. Kucherlapati, V. Baichwal, 1986, Springer US.

Lung cancer signatures in plasma based on proteome profiling of mouse tumor models.

Kwon-Sik Park, Vitor M Faça, Christopher J Kemp, 2011, Cancer cell.

DTNBP1 is associated with imaging phenotypes in schizophrenia

Arthur W Toga, Liberty S. Hamilton, Delbert Robinson, 2009, Human brain mapping.

The finished DNA sequence of human chromosome 12

Paul Havlak, Christian J. Buhay, Donna M. Muzny, 2006, Nature.

Development of a mouse model for sporadic and metastatic colon tumors and its use in assessing drug treatment

Umar Mahmood, Raju Kucherlapati, Kenneth E. Hung, 2010, Proceedings of the National Academy of Sciences.

Shared genetic causes of cardiac hypertrophy in children and adults.

Heidi L Rehm, Raju Kucherlapati, Hiroyuki Morita, 2008, The New England journal of medicine.

Onset of abnormal blood and lymphatic vessel function and interstitial hypertension in early stages of carcinogenesis.

Lei Xu, Dai Fukumura, Ricky T. Tong, 2006, Cancer research.