World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
56
Citations
11487
World Ranking
3503
National Ranking
137

Fadi F. Hamdan 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 Fadi F. Hamdan 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: 115 publications — 13th percentile

13% of scientists in this discipline score the same or lower.

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

Fadi F. Hamdan 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 Fadi F. Hamdan 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: 56 D-Index — 21st percentile

21% of scientists in this discipline score the same or lower.

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

Overview

Fadi F. Hamdan is affiliated with the University of Montreal in Canada. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, with particular focus on Genetics and Molecular Biology. Additional areas of study include Pediatrics, Perinatology and Child Health, Emergency Medicine, and Epidemiology.

The main research topics covered by Hamdan include:

  • Genomics and Rare Diseases
  • Genetics and Neurodevelopmental Disorders
  • Genomic variations and chromosomal abnormalities
  • Renal and related cancers
  • Pluripotent Stem Cells Research
  • Ethics and Legal Issues in Pediatric Healthcare
  • Trauma and Emergency Care Studies

Hamdan has contributed to several peer-reviewed papers, with research published in notable venues such as the Journal of Medical Genetics, bioRxiv (Cold Spring Harbor Laboratory), Epilepsia, Molecular Genetics and Metabolism, and Genetics in Medicine.

Some key publications include:

  • De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability, 2021, Journal of Medical Genetics
  • FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability, 2020, Epilepsia
  • Bi-allelic variants in WNT7B disrupt the development of multiple organs in humans, 2022, Journal of Medical Genetics
  • De novocoding variants in theAGO1gene cause a neurodevelopmental disorder with intellectual disability, 2020, bioRxiv (Cold Spring Harbor Laboratory)
  • First tier rapid whole genome sequencing increases diagnostic yield and changes management in children admitted in intensive care, 2021, Molecular Genetics and Metabolism

Frequent co-authors in Hamdan's work include:

  • Jacques L. Michaud
  • Nino Spataro
  • William B. Dobyns
  • Audrey Schalk
  • Margot A. Cousin

Best Publications

  • High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

    Fadi F. Hamdan;Candace T. Myers;Patrick Cossette;Philippe Lemay

  • De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

    Julie Gauthier;Nathalie Champagne;Ronald G. Lafrenière;Lan Xiong

  • De Novo Mutations in Moderate or Severe Intellectual Disability

    Fadi F. Hamdan;Myriam Srour;Jose-Mario Capo-Chichi;Hussein Daoud

  • Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.

    Fadi F. Hamdan;Julie Gauthier;Dan Spiegelman;Anne Noreau

  • Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

    Fadi F. Hamdan;Julie Gauthier;Yoichi Araki;Da-Ting Lin

  • Novel de novo SHANK3 mutation in autistic patients.

    Julie Gauthier;Dan Spiegelman;Amélie Piton;Ronald G. Lafrenière

  • SHANK1 Deletions in Males with Autism Spectrum Disorder

    Daisuke Sato;Anath C. Lionel;Anath C. Lionel;Claire S. Leblond;Claire S. Leblond;Claire S. Leblond;Aparna Prasad

  • Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

    Piton A;Gauthier J;Hamdan Ff;Lafrenière Rg

  • A critical role for β cell M3 muscarinic acetylcholine receptors in regulating insulin release and blood glucose homeostasis in vivo

    Dinesh Gautam;Sung-Jun Han;Fadi F. Hamdan;Jongrye Jeon

  • Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

    Julie Gauthier;Tabrez J. Siddiqui;Peng Huashan;Daisaku Yokomaku

  • Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts

    Philip Awadalla;Julie Gauthier;Rachel A. Myers;Rachel A. Myers;Ferran Casals

  • Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency

    Martin H. Berryer;Fadi F. Hamdan;Laura L. Klitten;Rikke S. Møller

  • De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

    Fadi F. Hamdan;Hussein Daoud;Daniel Rochefort;Amélie Piton

  • Rare Mutations in N-methyl-D-aspartate Glutamate Receptors in Autism Spectrum Disorders and Schizophrenia

    Tarabeux J;Tarabeux J;Tarabeux J;Kebir O;Kebir O;Gauthier J;Hamdan Ff

  • Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

    Silvia Cappello;Mary J Gray;Caroline Badouel;Caroline Badouel;Simona Lange

  • De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism.

    Fadi F. Hamdan;Hussein Daoud;Amélie Piton;Julie Gauthier

  • High-throughput screening of G protein-coupled receptor antagonists using a bioluminescence resonance energy transfer 1-based beta-arrestin2 recruitment assay.

    Fadi F. Hamdan;Martin Audet;Philippe Garneau;Jerry Pelletier

  • Mutations in the calcium-related gene IL1RAPL1 are associated with autism

    Amélie Piton;Jacques L. Michaud;Huashan Peng;Swaroop Aradhya

  • The genetic landscape of infantile spasms

    Jacques L. Michaud;Mathieu Lachance;Fadi F. Hamdan;Lionel Carmant

  • De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.

    Fadi F. Hamdan;Amélie Piton;Julie Gauthier;Anne Lortie

Frequent Co-Authors

Jacques L. Michaud
Jacques L. Michaud University of Montreal
Guy A. Rouleau
Guy A. Rouleau Montreal Neurological Institute and Hospital
Jürgen Wess
Jürgen Wess National Institutes of Health
Berge A. Minassian
Berge A. Minassian The University of Texas Southwestern Medical Center
Laurent Mottron
Laurent Mottron University of Montreal
Pierre Drapeau
Pierre Drapeau University of Montreal
Ridha Joober
Ridha Joober Douglas Mental Health University Institute
Amélie Piton
Amélie Piton University of Strasbourg
Marie-Odile Krebs
Marie-Odile Krebs Université Paris Cité
Eric Fombonne
Eric Fombonne Oregon Health & Science University

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