World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
51
Citations
10378
World Ranking
3862
National Ranking
2

Wasim Ahmad 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 Wasim Ahmad 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: 307 publications — 77th percentile

77% of scientists in this discipline score the same or lower.

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

Wasim Ahmad 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 Wasim Ahmad 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: 51 D-Index — 12th percentile

12% of scientists in this discipline score the same or lower.

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

Research.com Recognitions

  • 2015 - Fellow, The World Academy of Sciences
  • 2010 - Fellow of Pakistan Academy of Sciences

Overview

Wasim Ahmad is affiliated with Quaid-i-Azam University in Pakistan and has contributed extensively to the fields of Biochemistry, Genetics and Molecular Biology as well as Medicine. Their research work spans several subfields including Molecular Biology, Genetics, Cell Biology, Developmental Biology, and Artificial Intelligence.

Their recent publications cover a variety of topics and were published in several scientific venues. Notable papers include:

  • Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice (2021) published in Frontiers in Cell and Developmental Biology
  • Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment (2020) in Genes
  • Biallelic variants in four genes underlying recessive osteogenesis imperfecta (2020) in European Journal of Medical Genetics
  • Comparative analysis of deep neural network architectures for renewable energy forecasting: enhancing accuracy with meteorological and time-based features (2024) in Discover Sustainability
  • Clinical and genetic characterization of congenital lipoid adrenal hyperplasia (2020) in Clinical Dysmorphology

Their research focuses on diverse topics, including:

  • Congenital limb and hand anomalies
  • Hedgehog Signaling Pathway Studies
  • Genomic variations and chromosomal abnormalities
  • Hearing, Cochlea, Tinnitus, Genetics
  • Congenital heart defects research
  • Genetics and Neurodevelopmental Disorders
  • Wnt/β-catenin signaling in development and cancer

Wasim Ahmad has frequently published in these venues:

  • Journal of Human Genetics
  • Clinical Genetics
  • Molecular Syndromology
  • arXiv (Cornell University)
  • Genes

Their collaborative network includes frequent co-authors such as Asmat Ullah, Shabir Hussain, Shoaib Nawaz, Hammal Khan, and Khurram Liaqat.

They have been recognized with awards including:

  • Fellow, The World Academy of Sciences (2015)
  • Fellow of Pakistan Academy of Sciences (2010)

Best Publications

  • Alopecia Universalis Associated with a Mutation in the Human hairless Gene

    Wasim Ahmad;Muhammad Faiyaz ul Haque;Valeria Brancolini;Hui C. Tsou

  • Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion: Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris

    Ana Kljuic;Hisham Bazzi;John P Sundberg;Amalia Martinez-Mir

  • WDR62 is associated with the spindle pole and is mutated in human microcephaly

    Adeline K. Nicholas;Maryam Khurshid;Julie Désir;Ofélia P. Carvalho

  • Exposing the human nude phenotype

    Jorge Frank;Claudio Pignata;Andrei A. Panteleyev;David M. Prowse

  • Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

    Saima Riazuddin;Inna A Belyantseva;Arnaud P J Giese;Kwanghyuk Lee

  • Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

    Emma M. Jenkinson;Atteeq U. Rehman;Tom Walsh;Jill Clayton-Smith

  • Autosomal recessive primary microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum

    Saqib Mahmood;Wasim Ahmad;Muhammad J Hassan

  • Mutations in Orthologous Genes in Human Spondyloepimetaphyseal Dysplasia and the Brachymorphic Mouse

    Faiyaz ul Haque M;King Lm;Krakow D;Krakow D;Cantor Rm

  • Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.

    A. A. Panteleyev;R. Paus;W. Ahmad;J. P. Sundberg

  • Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

    Rob W.J. Collin;Ersan Kalay;Ersan Kalay;Muhammad Tariq;Theo Peters

  • Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

    Guntram Borck;Atteeq Ur Rehman;Atteeq Ur Rehman;Kwanghyuk Lee;Hans Martin Pogoda

  • Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

    Zubair M. Ahmed;Rizwan Yousaf;Rizwan Yousaf;Byung Cheon Lee;Shaheen N. Khan

  • Mutations in KARS, Encoding Lysyl-tRNA Synthetase, Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB89

    Regie Lyn P. Santos-Cortez;Kwanghyuk Lee;Zahid Azeem;Patrick J. Antonellis

  • Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family.

    Wasim Ahmad;Abraham Zlotogorski;Andrei A. Panteleyev;HaMut Lam

  • Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

    Julie M. Schultz;Shaheen N. Khan;Zubair M. Ahmed;Saima Riazuddin

  • Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome).

    M Faiyaz-Ul-Haque;W Ahmad;S H E Zaidi;S Haque

  • A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers

    W Ahmad;Alan D Irvine;H Lam;C Buckley

  • Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene

    Abraham Zlotogorski;Wasim Ahmad;Angela M. Christiano

  • Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.

    Regie Santos;Regie Santos;M. Wajid;Thanh Pham;J. Hussan

  • A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1.

    Wasim Ahmad;Valeria Brancolini;Muhammad Faiyaz ul Haque;HaMut Lam

Frequent Co-Authors

Suzanne M. Leal
Suzanne M. Leal Columbia University Medical Center
Angela M. Christiano
Angela M. Christiano Columbia University
Deborah A. Nickerson
Deborah A. Nickerson University of Washington
Michael J. Bamshad
Michael J. Bamshad University of Washington
Saima Riazuddin
Saima Riazuddin University of Maryland, Baltimore
Zubair M. Ahmed
Zubair M. Ahmed University of Maryland, Baltimore
Sheikh Riazuddin
Sheikh Riazuddin University of Health Sciences Lahore
Joshua D. Smith
Joshua D. Smith University of Washington
Jay Shendure
Jay Shendure University of Washington
Robert J. Morell
Robert J. Morell National Institutes of Health

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Each of these pathways can complement studies in Genetics and broaden your career opportunities in the fast-evolving healthcare sector.

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