Concepedia

Trilochan Sahoo

TS

Statistics

Publications

70

Citations

8K

H-Index

45

Active since

1994

Affiliations

Baylor College of Medicine(Current)

Texas Children's Hospital

Quest Diagnostics (United States)

Greenwood Genetic Center

Baylor Genetics

Trilochan Sahoo is an author at Baylor College of Medicine specializing in medicine, genetics, and pathology.

ORCID

Top concepts

Publications per year

1994–2022

70

Publications

70

Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

Trilochan Sahoo, Daniela del Gaudio, Jennifer R. German et al. · Nature Genetics · 2008 · 658 citations · Full text

, , +12

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

Nicola Brunetti‐Pierri, Jonathan S. Berg, Fernando Scaglia et al. · Nature Genetics · 2008 · 627 citations · Full text

, , +7

Mutations in the Gene Encoding KRIT1, a Krev-1/rap1a Binding Protein, Cause Cerebral Cavernous Malformations (CCM1)

Trilochan Sahoo, Eric W. Johnson, James W. Thomas et al. · Human Molecular Genetics · 1999 · 387 citations · Full text

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker, Blake C. Ballif, Erawati V. Bawle et al. · European Journal of Human Genetics · 2010 · 316 citations · Full text

, , +9

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders

Shay Ben‐Shachar, Brendan C. Lanpher, Jennifer R. German et al. · Journal of Medical Genetics · 2009 · 265 citations · Full text

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