Concepedia

Author

Waibhav Tembe

Translational Genomics Research Institute

Also Known As

Isaacs, Sarah D., Shripad A. Sinari, W Tembe, W. Tembe, Waibhav D Tembe, Waibhav D. Tembe, Waibhav Tembe, Waibhav Tembe (117037)

61

Publications

6.1K

Citations

26

H-Index

66

Concepts

All Affiliations

Translational Genomics Research InstituteMayo Clinic in ArizonaIllumina (United States)Texas A&M UniversityArizona State University
WT

About

Waibhav Tembe is an author at Translational Genomics Research Institute specializing in medicine, pathology, and engineering.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

10

1.9K

2

Engineering

6

6

638

3

Health Sciences

2

2

146

4

Public Health

2

2

1.4K

5

Management

1

1

379

Waibhav Tembe

×

29

Publications

5.2K

Citations

25

H-Index

YearCitations

Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays

Nils Homer, Szabolcs Szelinger, Margot Redman,

PLoS Genetics

2008

1.2K

Germline Mutations in <i>HOXB13</i> and Prostate-Cancer Risk

Charles M. Ewing, Anna M. Ray, Ethan M. Lange,

New England Journal of Medicine

2012

656

A map of human genome variation from population-scale sequencing

Richard Durbin, David L. Altshuler, Gonçalo R. Abecasis,

HAL (Le Centre pour la Communication Scientifique Directe)

2010

542

Whole-genome sequencing of multiple myeloma from diagnosis to plasma cell leukemia reveals genomic initiating events, evolution, and clonal tides

Jan B. Egan, Chang-Xin Shi, Waibhav Tembe,

Blood

2012

402

Profiles of Extracellular miRNA in Cerebrospinal Fluid and Serum from Patients with Alzheimer's and Parkinson's Diseases Correlate with Disease Status and Features of Pathology

Kasandra Burgos, Ivana Malenica, Raghu Metpally,

PLoS ONE

2014

387

Performance of feature-selection methods in the classification of high-dimension data

Jianping Hua, Waibhav Tembe, Edward R. Dougherty

Pattern Recognition

2008

379

GRM7 variants confer susceptibility to age-related hearing impairment

Rick A. Friedman, Lut Van Laer, Matthew J. Huentelman,

Human Molecular Genetics

2008

208

Identification of extracellular miRNA in human cerebrospinal fluid by next-generation sequencing

Kasandra Burgos, Ashkan Javaherian, Roberto Bomprezzi,

RNA

2013

187

Identification of the Genetic Basis for Complex Disorders by Use of Pooling-Based Genomewide Single-Nucleotide–Polymorphism Association Studies

John V. Pearson, Matthew J. Huentelman, Rebecca F. Halperin,

The American Journal of Human Genetics

2006

155

Personalized treatment of Sézary syndrome by targeting a novel <i><scp>CTLA</scp>4</i>:<i><scp>CD</scp>28</i> fusion

Aleksandar Sekulić, Winnie S. Liang, Waibhav Tembe,

Molecular Genetics & Genomic Medicine

2014

83

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