World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
52
Citations
9052
World Ranking
3801
National Ranking
1638

Trilochan Sahoo publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Trilochan Sahoo sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 84 publications — 3rd percentile

3% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Trilochan Sahoo D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Trilochan Sahoo sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 52 D-Index — 14th percentile

14% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

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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