Concepedia

Author

Thashi Bharadwaj

Columbia University Irving Medical CenterORCID

Also Known As

T P Bharadwaj, T.P.R. Bharadwaj, Thashi Bharadwaj

37

Publications

255

Citations

9

H-Index

17

Concepts

All Affiliations

Columbia University Irving Medical CenterUniversity of Cape TownUniversity of GhanaQuaid-i-Azam University
TB

About

Thashi Bharadwaj is an author at Columbia University Irving Medical Center specializing in molecular diagnostics, medicine, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

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Medicine

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33

2

Arts

1

1

14

3

Molecular Biology

1

1

14

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Molecular Genetics

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14

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Molecular Medicine

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19

Thashi Bharadwaj

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9

Publications

181

Citations

9

H-Index

YearCitations

Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment

Isabelle Schrauwen, Khurram Liaqat, Isabelle Schatteman,

Genes

2020

40

Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise strategy in the genomic era

Zhiying Xie, Chengyue Sun, Yilin Liu,

Journal of Medical Genetics

2020

29

Analysis of karyotype, SCE, and point mutation of RAS oncogene in Indian MDS patients

Ahmed M. Mansoor, Thashi Bharadwaj, Shriram Sethuraman,

Cancer Genetics and Cytogenetics

1993

19

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

Ambroise Wonkam, Samuel Mawuli Adadey, Isabelle Schrauwen,

Communications Biology

2022

19

Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment

Edmond Wonkam‐Tingang, Isabelle Schrauwen, Kevin Esoh,

Genes

2020

18

ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment

Thashi Bharadwaj, Isabelle Schrauwen, Sakina Rehman,

European Journal of Human Genetics

2021

15

Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

Adebolajo A. Adeyemo, Rabia Faridi, Parna Chattaraj,

European Journal of Human Genetics

2021

15

Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

Samuel Mawuli Adadey, Isabelle Schrauwen, Elvis Twumasi Aboagye,

Journal of Human Genetics

2021

14

A novel variant in <i>DMXL2</i> gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family

Edmond Wonkam‐Tingang, Isabelle Schrauwen, Kevin Esoh,

Experimental Biology and Medicine

2021

12

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