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Overview

Trilochan Sahoo is affiliated with Baylor College of Medicine in the United States. Their research spans multiple areas within medicine and biochemistry, genetics, and molecular biology, focusing particularly on genetics, pediatrics, perinatology, child health, public health, immunology, and neurology.

Their primary research topics include prenatal screening and diagnostics, gestational trophoblastic disease studies, reproductive system and pregnancy, Parkinson's disease mechanisms and treatments, Alzheimer's disease research and treatments, neurological disorders and treatments, and craniofacial disorders and treatments.

The scientist's recent publications include:

  • "The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriages," 2022, Reproductive BioMedicine Online
  • "Unravelling the Proteinopathic Engagement of α-Synuclein, Tau, and Amyloid Beta in Parkinson's Disease: Mitochondrial Collapse as a Pivotal Driver of Neurodegeneration," 2025, Neurochemical Research
  • "Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly," 2020, Clinical Dysmorphology
  • "Correction: Comprehensive analysis of 204 sporadic hydatidiform moles: revisiting risk factors and their correlations with the molar genotypes," 2020, Modern Pathology
  • "P-553 Women with molar pregnancies have a genetic susceptibility to aneuploid miscarriages," 2021, Human Reproduction

Frequent co-authors who have collaborated with Trilochan Sahoo include:

  • Karine Hovanes
  • Rima Slim
  • Yassemine Khawajkie
  • Lori Hoffner
  • L. Tan

Their publications have appeared in multiple scientific venues like:

  • Reproductive BioMedicine Online
  • Neurochemical Research
  • Clinical Dysmorphology
  • Modern Pathology
  • Human Reproduction

Trilochan Sahoo's body of work integrates clinical subjects and molecular approaches related to prenatal and reproductive health as well as neurological disease mechanisms. Their research contributes to understanding conditions such as miscarriage, molar pregnancies, neurodegeneration in Parkinson's disease, and craniofacial disorders through genetic and biochemical perspectives.

Best Publications

  • 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;Marwan Shinawi

  • 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;John Belmont

  • 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;Peter M. Kuehl

  • 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;Richard E Person

  • Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

    Jonathan S. Berg;Nicola Brunetti-Pierri;Sarika U. Peters;Sung Hae L. Kang

  • Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases

    Xinyan Lu;Chad A. Shaw;Ankita Patel;Jiangzhen Li

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

    S. Ben-Shachar;B. Lanpher;J. R. German;M. Qasaymeh

  • Increased LIS1 expression affects human and mouse brain development

    Weimin Bi;Tamar Sapir;Oleg A. Shchelochkov;Feng Zhang

  • Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

    Sau W. Cheung;Chad A. Shaw;Daryl A. Scott;Ankita Patel

  • Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching

    Claudia M.B. Carvalho;Feng Zhang;Pengfei Liu;Ankita Patel

  • Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.

    Trilochan Sahoo;Sau Wai Cheung;Patricia Ward;Sandra Darilek

  • A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.

    Yong Hui Jiang;Trilochan Sahoo;Ron C. Michaelis;Dani Bercovich

  • Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis

    Xin Yan Lu;Mai T. Phung;Chad A. Shaw;Kim Pham

  • Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

    Lina Shao;Chad A. Shaw;Xin Yan Lu;Trilochan Sahoo

  • A neurodevelopmental survey of Angelman syndrome with genotype-phenotype correlations.

    Jennifer K. Gentile;Wen-Hann Tan;Lucia T. Horowitz;Carlos A. Bacino

  • Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12

    Sandesh Chakravarthy Sreenath Nagamani;Ayelet Erez;Joseph Shen;Chumei Li

  • Cerebral folate deficiency with developmental delay, autism, and response to folinic acid

    P. Moretti;T. Sahoo;K. Hyland;T. Bottiglieri

  • 22q13.3 deletion syndrome: Clinical and molecular analysis using array CGH†

    S. U. Dhar;D. Del Gaudio;J. R. German;S. U. Peters

  • Microdeletions including YWHAE in the Miller–Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment

    S C Sreenath Nagamani;F Zhang;O A Shchelochkov;W Bi

  • Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders.

    Jill A Rosenfeld;Blake C Ballif;Beth S Torchia;Trilochan Sahoo

Frequent Co-Authors

Arthur L. Beaudet
Arthur L. Beaudet Baylor College of Medicine
Ankita Patel
Ankita Patel Baylor College of Medicine
Carlos A. Bacino
Carlos A. Bacino Baylor College of Medicine
Pawel Stankiewicz
Pawel Stankiewicz Baylor College of Medicine
James R. Lupski
James R. Lupski Baylor College of Medicine
Sau Wai Cheung
Sau Wai Cheung Baylor College of Medicine
A. Craig Chinault
A. Craig Chinault Baylor College of Medicine
Chad A. Shaw
Chad A. Shaw Baylor College of Medicine
Seema R. Lalani
Seema R. Lalani Baylor College of Medicine
Marwan Shinawi
Marwan Shinawi Washington University in St. Louis

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