World's Best Scientists 2026 revealed!
Maria Martinez

Maria Martinez

D-Index & Metrics

Genetics

D-Index
55
Citations
17938
World Ranking
3543
National Ranking
181

Maria Martinez 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 Maria Martinez 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: 156 publications — 33rd percentile

33% of scientists in this discipline score the same or lower.

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

Maria Martinez 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 Maria Martinez 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: 55 D-Index — 19th percentile

19% of scientists in this discipline score the same or lower.

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

Overview

Maria Martinez is affiliated with Inserm in France and has contributed extensively to the fields of medicine, biochemistry, genetics, and molecular biology. Their research spans core subfields including molecular biology, genetics, clinical psychology, psychiatry and mental health, and neurology.

The scientist's work addresses various topics such as genetic associations and epidemiology, RNA regulation and disease, bioinformatics and genomic networks, Parkinson's disease mechanisms and treatments, neurological diseases and metabolism, RNA research and splicing, and RNA modifications and cancer.

Prominent recent publications by Maria Martinez include:

  • Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome, 2021, Nature Communications
  • Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets, 2021, JAMA Neurology
  • Identification of sixteen novel candidate genes for late onset Parkinson's disease, 2021, Molecular Neurodegeneration
  • Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information, 2020, Nature Communications
  • A national programme to scale-up decentralised hepatitis C point-of-care testing and treatment in Australia, 2023, The Lancet. Gastroenterology & Hepatology

Maria Martinez frequently collaborates with several researchers, including:

  • Jean-Christophe Corvol
  • Demis A. Kia
  • Daniah Trabzuni
  • Patrick A. Lewis
  • Sebastian Guelfi

The publications of Maria Martinez appear in notable venues such as:

  • Nature Communications (3 publications)
  • European Psychiatry (3 publications)
  • Alzheimer's & Dementia (2 publications)
  • JAMA Neurology (1 publication)
  • Molecular Neurodegeneration (1 publication)

Best Publications

  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    Mike A Nalls;Cornelis Blauwendraat;Costanza L Vallerga;Karl Heilbron

  • Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

    Mike A Nalls;Nathan Pankratz;Christina M. Lill;Chuong B. Do

  • Analysis of shared heritability in common disorders of the brain

    Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters

  • Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum

    Dominique Campion;Cécile Dumanchin;Didier Hannequin;Bruno Dubois

  • Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.

    Michael A Nalls;Vincent Plagnol;Dena G Hernandez

  • Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

    Anne Philippe;Anne Philippe;Maria Martinez;Michel Guilloud-Bataille;Christopher Gillberg

  • New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study

    François Cornélis;Sabine Fauré;Maria Martinez;Jean-François Prud’homme

  • Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: the PDGene database.

    Christina M. Lill;Johannes T. Roehr;Johannes T. Roehr;Matthew B. McQueen;Fotini K. Kavvoura;Fotini K. Kavvoura;Fotini K. Kavvoura

  • No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: Implications for psychiatric genetics

    Alan R. Sanders;Jubao Duan;Douglas F. Levinson;Jianxin Shi

  • Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

    A. Beilina;I. N. Rudenko;A. Kaganovich;L. Civiero

  • Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.

    Dominique Campion;Dominique Campion;Jean-Michel Flaman;Alexis Brice;Didier Hannequin

  • Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

    Qiuhe Cao;Maria Martinez;Jing Zhang;Alan R. Sanders

  • Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.

    Yannick Allanore;Yannick Allanore;Mohamad Saad;Philippe Dieudé;Jérôme Avouac;Jérôme Avouac

  • A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32

    Mathilde Varret;Jean-Pierre Rabès;Bruno Saint-Jore;Ana Cenarro

  • Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease

    M.F. Keller;M. Saad;M. Saad;J. Bras;F. Bettella

  • Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

    Mike A Nalls;Cory Y McLean;Jacqueline Rick;Shirley Eberly

  • Genomewide Linkage Scan of 409 European-Ancestry and African American Families with Schizophrenia: Suggestive Evidence of Linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the Combined Sample

    Brian K. Suarez;Jubao Duan;Alan R. Sanders;Anthony L. Hinrichs

  • Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

    Mohamad Saad;Mohamad Saad;Suzanne Lesage;Suzanne Lesage;Suzanne Lesage;Aude Saint-Pierre;Aude Saint-Pierre;Jean-Christophe Corvol

  • Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex

    H Bickeböller;D Campion;A Brice;P Amouyel

  • Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.

    R.S. (R. S.) Desikan;A.J. (A. J.) Schork;Y. Wang;Y. Wang;Aree Witoelar

Frequent Co-Authors

Alexis Brice
Alexis Brice Institut du Cerveau
Thomas Gasser
Thomas Gasser University of Tübingen
Peter Heutink
Peter Heutink German Center for Neurodegenerative Diseases
Dena G. Hernandez
Dena G. Hernandez National Institutes of Health
Nicholas W. Wood
Nicholas W. Wood University College London
John Hardy
John Hardy University College London
Andrew B. Singleton
Andrew B. Singleton National Institutes of Health
Dominique Campion
Dominique Campion University of Rouen
Mike A. Nalls
Mike A. Nalls National Institutes of Health

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Related Online Degrees & Career Pathways

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