World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
59
Citations
12701
World Ranking
3239
National Ranking
1407

Brett H. Graham 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 Brett H. Graham 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: 135 publications — 23rd percentile

23% of scientists in this discipline score the same or lower.

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

Brett H. Graham 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 Brett H. Graham 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: 59 D-Index — 27th percentile

27% of scientists in this discipline score the same or lower.

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

Overview

Brett H. Graham is affiliated with Baylor College of Medicine in the United States. Their research spans primarily the fields of Biochemistry, Genetics, and Molecular Biology, with a substantial focus in Medicine. The subfields of their studies include Molecular Biology, Genetics, Physiology, Clinical Biochemistry, and Epidemiology.

The main topics covered in their research encompass:

  • Metabolism and Genetic Disorders
  • Mitochondrial Function and Pathology
  • Genomics and Rare Diseases
  • Genomic Variations and Chromosomal Abnormalities
  • Diet and Metabolism Studies
  • Adipose Tissue and Metabolism
  • Liver Disease Diagnosis and Treatment

They have contributed to multiple frequent publication venues, including:

  • Genetics in Medicine Open
  • Molecular Genetics and Metabolism
  • Genetics in Medicine
  • American Journal of Medical Genetics Part A
  • Translational Psychiatry

Among the notable recent papers authored or coauthored by Brett H. Graham are:

  • Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male mice, 2020, Translational Psychiatry
  • Dietary Choline Supplements, but Not Eggs, Raise Fasting TMAO Levels in Participants with Normal Renal Function: A Randomized Clinical Trial, 2021, The American Journal of Medicine
  • UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism, 2020, The American Journal of Human Genetics
  • MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia, 2021, Annals of Neurology
  • Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit, 2023, International Journal of Molecular Sciences

Their frequent coauthors include Erin Conboy, Patrick J. Gillespie, Kayla Treat, Benjamin M. Helm, and Francesco Vetrini. The collaboration with these colleagues indicates active partnerships in their research projects.

Best Publications

  • Glial Lipid Droplets and ROS Induced by Mitochondrial Defects Promote Neurodegeneration

    Lucy Liu;Ke Zhang;Hector Sandoval;Shinya Yamamoto;Shinya Yamamoto

  • 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

  • A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

    Brett H. Graham;Katrina G. Waymire;Barbara Cottrell;Ian A. Trounce

  • Efficacy and safety of nerinetide for the treatment of acute ischaemic stroke (ESCAPE-NA1): a multicentre, double-blind, randomised controlled trial.

    Michael D Hill;Mayank Goyal;Bijoy K Menon;Raul G Nogueira

  • Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

    Marwan Shinawi;Pengfei Liu;Sung Hae L Kang;Joseph Shen

  • Sox9 and NFIA Coordinate a Transcriptional Regulatory Cascade during the Initiation of Gliogenesis

    Peng Kang;Hyun Kyoung Lee;Stacey M. Glasgow;Meggie Finley

  • Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management

    Linyan Meng;Linyan Meng;Mohan Pammi;Anirudh Saronwala;Pilar Magoulas;Pilar Magoulas

  • Marked changes in mitochondrial DNA deletion levels in Alzheimer brains

    M Corral-Debrinski;T Horton;M T Lott;J M Shoffner

  • Fatty Acid Oxidation-Driven Src Links Mitochondrial Energy Reprogramming and Oncogenic Properties in Triple-Negative Breast Cancer

    Jun Hyoung Park;Sajna Vithayathil;Santosh Kumar;Pi Lin Sung;Pi Lin Sung

  • The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

    Claire Redin;Claire Redin;Harrison Brand;Harrison Brand;Ryan L Collins;Ryan L Collins;Tammy Kammin

  • Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathway

    Gregory M. Enns;Vandana Shashi;Matthew Bainbridge;Michael J. Gambello

  • Lessons learned from additional research analyses of unsolved clinical exome cases

    Mohammad K. Eldomery;Mohammad K. Eldomery;Zeynep Coban-Akdemir;Tamar Harel;Jill A. Rosenfeld

  • Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans

    Vafa Bayat;Isabelle Thiffault;Isabelle Thiffault;Manish Jaiswal;Martine Tétreault

  • MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.

    Julia Wang;Rami Al-Ouran;Yanhui Hu;Seon-Young Kim

  • Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance

    Penelope E. Bonnen;John W. Yarham;Arnaud Besse;Ping Wu

  • Clinical course of sly syndrome (mucopolysaccharidosis type VII)

    Adriana M Montaño;Ngu Lock-Hock;Robert D Steiner;Brett H Graham

  • De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome

    Matthew N Bainbridge;Hao Hu;Donna M Muzny;Luciana Musante

  • Recurrent De Novo and Biallelic Variation of ATAD3A, Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes.

    Tamar Harel;Wan Hee Yoon;Caterina Garone;Shen Gu

  • Mitochondrial biology, degenerative diseases and aging

    Douglas C. Wallace;Michael D. Brown;Simon Melov;Brett Graham

  • The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease

    Rachel B. Ramoni;Rachel B. Ramoni;John J. Mulvihill;David R. Adams;Patrick Allard

Frequent Co-Authors

William J. Craigen
William J. Craigen Baylor College of Medicine
Hugo J. Bellen
Hugo J. Bellen Baylor College of Medicine
Seema R. Lalani
Seema R. Lalani Baylor College of Medicine
Lee-Jun C. Wong
Lee-Jun C. Wong Baylor College of Medicine
Jill A. Rosenfeld
Jill A. Rosenfeld Baylor College of Medicine
Brendan Lee
Brendan Lee Baylor College of Medicine
Christine M. Eng
Christine M. Eng Baylor College of Medicine
James R. Lupski
James R. Lupski Baylor College of Medicine
Donna M. Muzny
Donna M. Muzny Baylor College of Medicine
Richard A. Gibbs
Richard A. Gibbs Baylor College of Medicine

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