World's Best Scientists 2026 revealed!
Michael A. Walter

Michael A. Walter

D-Index & Metrics

Genetics

D-Index
52
Citations
9383
World Ranking
3795
National Ranking
145

Michael A. Walter 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 Michael A. Walter 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: 182 publications — 43rd percentile

43% of scientists in this discipline score the same or lower.

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

Michael A. Walter 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 Michael A. Walter 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

Michael A. Walter is affiliated with the University of Alberta in Canada. Their research spans fields primarily in Biochemistry, Genetics and Molecular Biology, with significant work also in Medicine. The scientist's subfields of study include Molecular Biology, Radiology, Nuclear Medicine and Imaging, Cell Biology, Ophthalmology, and Genetics.

Their research covers topics such as Retinal Development and Disorders, FOXO transcription factor regulation, Retinopathy of Prematurity Studies, Genomics and Chromatin Dynamics, DNA Repair Mechanisms, Genomics and Phylogenetic Studies, and Cellular transport and secretion.

Michael A. Walter has contributed to several scholarly publications including:

  • "FOXQ1 is Differentially Expressed Across Breast Cancer Subtypes with Low Expression Associated with Poor Overall Survival" (2021), published in Breast Cancer Targets and Therapy
  • "Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins" (2021), published in Molecules
  • "Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma" (2023), published in International Journal of Molecular Sciences
  • "Ocular genetics in the genomics age" (2020), published in American Journal of Medical Genetics Part C Seminars in Medical Genetics
  • "The Explorer's Guide to Biology: A Free Multimedia Educational Resource to Promote Deep Learning and Understanding of the Scientific Process" (2022), published in Journal of Microbiology and Biology Education

Frequent publication venues for Michael A. Walter include:

  • American Journal of Medical Genetics Part C Seminars in Medical Genetics
  • Breast Cancer Targets and Therapy
  • Molecules
  • International Journal of Molecular Sciences
  • Journal of Microbiology and Biology Education

Repeated collaborations appear with coauthors including:

  • Tim Footz
  • Fahed Elian
  • Ubah Are
  • Paulo S Nuin
  • Todd McMullen

Through their work, Walter engages with both experimental and genomic aspects of molecular biology and medicine, contributing to the understanding of ocular genetics, pigment-related disorders, and broader molecular evolutionary studies. Their detailed study of proteins relevant to pigmentation and associated disorders intersects with ophthalmology and biochemistry fields, addressing complex genetic and cellular mechanisms.

Best Publications

  • Circular transcripts of the testis-determining gene Sry in adult mouse testis

    Blanche Capel;Amanda Swain;Silvia Nicolis;Adam Hacker

  • A method for constructing radiation hybrid maps of whole genomes

    Michael A. Walter;Dominique J. Spillett;Philip Thomas;Jean Weissenbach

  • The Forkhead/Winged Helix Gene Mf1 Is Disrupted in the Pleiotropic Mouse Mutation congenital hydrocephalus

    Tsutomu Kume;Ke Yu Deng;Virginia Winfrey;Douglas B. Gould

  • Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

    Alan J. Mears;Tim Jordan;Farideh Mirzayans;Stéphane Dubois

  • FOXC1 is a potential prognostic biomarker with functional significance in basal-like breast cancer

    Partha S. Ray;Jinhua Wang;Ying Qu;Myung Shin Sim

  • ROLES FOR THE WINGED HELIX TRANSCRIPTION FACTORS MF1 AND MFH1 IN CARDIOVASCULAR DEVELOPMENT REVEALED BY NONALLELIC NONCOMPLEMENTATION OF NULL ALLELES

    Glenn E. Winnier;Tsutomu Kume;Keyu Deng;Rhonda Rogers

  • Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors

    Suzana Gispert;Dajana Parganlija;Michael Klinkenberg;Stefan Dröse

  • Molecular genetics of Axenfeld–Rieger malformations

    Matthew A. Lines;Kathy Kozlowski;Michael A. Walter

  • Mutation of the PAX6 gene in patients with autosomal dominant keratitis.

    F Mirzayans;W G Pearce;I M MacDonald;M A Walter

  • Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.

    M. Hermina Strungaru;Irina Dinu;Michael A. Walter

  • Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies

    Ming Ye;Karyn M. Berry-Wynne;Mika Asai-Coakwell;Periasamy Sundaresan

  • Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis

    Fred B. Berry;Matthew A. Lines;J. Martin Oas;Tim Footz

  • Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome

    Stephen C. Kulak;Kathy Kozlowski;Elena V. Semina;William G. Pearce

  • SOX Genes: Architects of Development

    Heather M. Prior;Michael A. Walter

  • Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders

    Kathy Kozlowski;Michael A. Walter

  • Axenfeld-Rieger syndrome.

    Morteza Seifi;Michael A Walter

  • Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25

    Farideh Mirzayans;Douglas B Gould;E Héon;Gail D Billingsley

  • Analyses of the Effects That Disease-Causing Missense Mutations Have on the Structure and Function of the Winged-Helix Protein FOXC1

    Ramsey A. Saleem;Sharmila Banerjee-Basu;Fred B. Berry;Andreas D. Baxevanis

  • Complete physical map of the human immunoglobulin heavy chain constant region gene complex

    Marten H. Hofker;Michael A. Walter;Diane W. Cox

  • Genotype–Phenotype Correlation in Axenfeld–Rieger Malformation (ARM) and Glaucoma Patients With FOXC1 and PITX2 Mutations

    M.H. Strungaru;M.A. Walter

Frequent Co-Authors

Jane C. Sowden
Jane C. Sowden University College London
Robert Ritch
Robert Ritch New York Eye and Ear Infirmary
Shomi S. Bhattacharya
Shomi S. Bhattacharya University College London
Peng T. Khaw
Peng T. Khaw University College London
Elise Héon
Elise Héon University of Toronto
Elena V. Semina
Elena V. Semina Medical College of Wisconsin
Andreas D. Baxevanis
Andreas D. Baxevanis National Institutes of Health
Sue Povey
Sue Povey University College London
Janey L. Wiggs
Janey L. Wiggs Massachusetts Eye and Ear Infirmary

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