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D-Index & Metrics

Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Genetics 68 2414 2294 1086 1021 199 20979

Nathan Pankratz publications per year

The chart shows the history of publications by Nathan Pankratz between 2001 and 2026, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Nathan Pankratz published across 26 years, from 2001 to 2026, averaging 16.5 papers a year. Output peaked at 108 publications in 2023. 49 of the 430 publications appeared in the last two years.

No. of publications
25 50 75 100
Bar chart. Horizontal axis: year, 2001 to 2026. Vertical axis: number of publications, 0 to 108. Peak 108 publications in 2023. 2001: 2 publications 2002: 2 publications 2003: 4 publications 2004: 3 publications 2005: 4 publications 2006: 5 publications 2007: 5 publications 2008: 2 publications 2009: 8 publications 2010: 8 publications 2011: 10 publications 2012: 6 publications 2013: 6 publications 2014: 9 publications 2015: 7 publications 2016: 13 publications 2017: 16 publications 2018: 13 publications 2019: 24 publications 2020: 24 publications 2021: 19 publications 2022: 27 publications 2023: 108 publications 2024: 56 publications 2025: 48 publications 2026: 1 publication
2001 2026

430 publications in total across all disciplines

View publications per year as a table
Nathan Pankratz: publications per year, 2001 to 2026
Year Publications
2001 2
2002 2
2003 4
2004 3
2005 4
2006 5
2007 5
2008 2
2009 8
2010 8
2011 10
2012 6
2013 6
2014 9
2015 7
2016 13
2017 16
2018 13
2019 24
2020 24
2021 19
2022 27
2023 108
2024 56
2025 48
2026 1
Total 430
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Nathan Pankratz 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 Nathan Pankratz sits on this spectrum.

No. of scientists
50 100 150 200
Bar chart with 67 bars. Horizontal axis: publications, 45–54 to 703+. Vertical axis: number of scientists, 0 to 217. Most scientists, 217, have 125–134 publications. The last bar groups every scientist with 703 publications or more. The highlighted bar, 195–204 publications, is where this scientist sits. 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
45–54 publications 703+

This scientist: 199 publications — 50th percentile

50% of scientists in this discipline score the same or lower.

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

View publications distribution as a table
Number of Genetics scientists by publication count, Research.com 2026 ranking edition. Based on 4,342 ranked scientists.
Publications Scientists This scientist
45–54 6
55–64 10
65–74 35
75–84 84
85–94 102
95–104 151
105–114 175
115–124 203
125–134 217
135–144 205
145–154 193
155–164 188
165–174 170
175–184 178
185–194 164
195–204 173 199
205–214 159
215–224 134
225–234 143
235–244 105
245–254 114
255–264 92
265–274 88
275–284 87
285–294 80
295–304 62
305–314 75
315–324 67
325–334 60
335–344 52
345–354 40
355–364 48
365–374 47
375–384 46
385–394 31
395–404 27
405–414 40
415–424 30
425–434 43
435–444 29
445–454 14
455–464 28
465–474 21
475–484 21
485–494 22
495–504 17
505–514 12
515–524 11
525–534 8
535–544 8
545–554 14
555–564 4
565–574 11
575–584 5
585–594 11
595–604 12
605–614 7
615–624 6
625–634 10
635–644 9
645–654 10
655–664 6
665–674 6
675–684 6
685–694 4
695–702 6
703+ 100
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Nathan Pankratz 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 Nathan Pankratz sits on this spectrum.

No. of scientists
50 100 150
Bar chart with 61 bars. Horizontal axis: D-Index, 40–41 to 160+. Vertical axis: number of scientists, 0 to 191. Most scientists, 191, have 62–63 D-Index. The last bar groups every scientist with 160 D-Index or more. The highlighted bar, 68–69 D-Index, is where this scientist sits. 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
40–41 D-Index 160+

This scientist: 68 D-Index — 45th percentile

45% of scientists in this discipline score the same or lower.

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

View D-Index distribution as a table
Number of Genetics scientists by D-index, Research.com 2026 ranking edition. Based on 4,342 ranked scientists.
D-Index Scientists This scientist
40–41 24
42–43 52
44–45 84
46–47 112
48–49 118
50–51 141
52–53 143
54–55 145
56–57 179
58–59 162
60–61 175
62–63 191
64–65 172
66–67 184
68–69 164 68
70–71 158
72–73 150
74–75 136
76–77 127
78–79 127
80–81 111
82–83 110
84–85 110
86–87 84
88–89 102
90–91 66
92–93 72
94–95 70
96–97 54
98–99 60
100–101 49
102–103 55
104–105 45
106–107 42
108–109 28
110–111 39
112–113 25
114–115 31
116–117 29
118–119 34
120–121 29
122–123 29
124–125 18
126–127 27
128–129 22
130–131 16
132–133 11
134–135 17
136–137 12
138–139 21
140–141 4
142–143 9
144–145 14
146–147 6
148–149 10
150–151 7
152–153 9
154–155 8
156–157 8
158–159 9
160+ 96
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Overview

Nathan Pankratz is affiliated with the University of Minnesota in the United States. Their research spans multiple fields within biomedical science, with a particular emphasis on Medicine and Biochemistry, Genetics, and Molecular Biology. The focus of their work includes several specialized subfields such as Genetics, Molecular Biology, Hematology, Surgery, and Pulmonary and Respiratory Medicine.

The scientist's research covers a broad range of topics, which include:

  • Genetic Associations and Epidemiology
  • Mitochondrial Function and Pathology
  • Blood groups and transfusion
  • Genomics and Rare Diseases
  • Metabolism and Genetic Disorders
  • Epigenetics and DNA Methylation
  • RNA modifications and cancer

Nathan Pankratz has contributed to peer-reviewed journals with papers in high-impact publication venues. Some of the frequent venues for their work are:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Nature Communications
  • Journal of the Endocrine Society
  • Cancer Research

Recent notable papers authored or co-authored by Nathan Pankratz include:

  • The Polygenic and Monogenic Basis of Blood Traits and Diseases, 2020, Cell
  • Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations, 2020, Cell
  • Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma, 2020, JAMA Oncology
  • Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes, 2020, Circulation Genomic and Precision Medicine
  • Evaluation of mitochondrial DNA copy number estimation techniques, 2020, PLoS ONE

Collaboration is a significant aspect of Nathan Pankratz's research career. The scientist has worked frequently with several co-authors, including:

  • Bruce M. Psaty
  • Jerome I. Rotter
  • Laura M. Raffield
  • Stephen S. Rich
  • Eric Boerwinkle

Best Publications

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.

    Daniel Taliun;Daniel N. Harris;Michael D. Kessler;Jedidiah Carlson;Jedidiah Carlson

  • 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

  • The polygenic and monogenic basis of blood traits and diseases

    Dragana Vuckovic;Erik L. Bao;Parsa Akbari;Caleb A. Lareau

  • Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.

    Ming-Huei Chen;Laura M Raffield;Abdou Mousas;Saori Sakaue

  • 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

  • Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.

    William C. Nichols;Nathan D Pankratz;Dena Hernandez;Coro Paisán-Ruíz;Coro Paisán-Ruíz

  • Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

    Nathan Pankratz;Jemma B. Wilk;Jeanne C. Latourelle;Anita L. DeStefano

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

    Daniel Taliun;Daniel N. Harris;Michael D. Kessler;Jedidiah Carlson;Jedidiah Carlson

  • A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    Michael A. Nalls;Raquel Duran;Grisel Lopez;Marzena Kurzawa-Akanbi

  • Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

    Li Shen;Sungeun Kim;Shannon L. Risacher;Kwangsik Nho

  • Translation initiator EIF4G1 mutations in familial Parkinson disease

    Marie Christine Chartier-Harlin;Marie Christine Chartier-Harlin;Justus C. Dachsel;Carles Vilariño-Güell;Sarah J. Lincoln

  • Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease.

    Ken Y. Hui;Heriberto Fernandez-Hernandez;Jianzhong Hu;Adam Schaffner

  • Meta-analysis of Parkinson's Disease: Identification of a Novel Locus, RIT2

    Nathan Pankratz;Gary W. Beecham;Anita L. Destefano;Ted M. Dawson

  • Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci

    Folkert W. Asselbergs;Yiran Guo;Yiran Guo;Erik P A Van Iperen;Suthesh Sivapalaratnam

  • Voxelwise genome-wide association study (vGWAS)

    Jason L. Stein;Xue Hua;Suh Lee;April J. Ho

  • A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

    April J. Ho;Jason L. Stein;Xue Hua;Suh Lee

  • Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

    Tatiana Foroud;S. K. Uniacke;L. Liu;Nathan D Pankratz

  • Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

    W. C. Nichols;W. C. Nichols;N. Pankratz;D. K. Marek;M. W. Pauciulo

  • Genetics of Parkinson disease.

    Nathan D Pankratz;Tatiana Foroud

  • The Polygenic and Monogenic Basis of Blood Traits and Diseases

    Dragana Vuckovic;Dragana Vuckovic;Erik L. Bao;Erik L. Bao;Parsa Akbari;Caleb A. Lareau;Caleb A. Lareau

Frequent Co-Authors

Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Tatiana Foroud
Tatiana Foroud Indiana University
Alexander P. Reiner
Alexander P. Reiner University of Washington
Nicholas L. Smith
Nicholas L. Smith University of Washington
Bruce M. Psaty
Bruce M. Psaty University of Washington
Kent D. Taylor
Kent D. Taylor David Geffen School of Medicine at UCLA
Jennifer A. Brody
Jennifer A. Brody University of Washington
Myriam Fornage
Myriam Fornage The University of Texas Health Science Center at Houston
James S. Pankow
James S. Pankow University of Minnesota
Jerome I. Rotter
Jerome I. Rotter UCLA Medical Center

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