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Stuart Schwartz

D-Index & Metrics

Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Genetics 71 2174 2067 986 925 228 21335

Stuart Schwartz publications per year

The chart shows the history of publications by Stuart Schwartz between 1980 and 2026, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Stuart Schwartz published across 47 years, from 1980 to 2026, averaging 5.9 papers a year. Output peaked at 24 publications in 2023. 7 of the 277 publications appeared in the last two years.

No. of publications
5 10 15 20
Bar chart. Horizontal axis: year, 1980 to 2026. Vertical axis: number of publications, 0 to 24. Peak 24 publications in 2023. 1980: 1 publication 1981: 0 publications 1982: 0 publications 1983: 3 publications 1984: 2 publications 1985: 4 publications 1986: 5 publications 1987: 1 publication 1988: 1 publication 1989: 6 publications 1990: 5 publications 1991: 2 publications 1992: 7 publications 1993: 10 publications 1994: 8 publications 1995: 11 publications 1996: 11 publications 1997: 15 publications 1998: 11 publications 1999: 14 publications 2000: 13 publications 2001: 7 publications 2002: 11 publications 2003: 5 publications 2004: 12 publications 2005: 8 publications 2006: 5 publications 2007: 2 publications 2008: 8 publications 2009: 3 publications 2010: 2 publications 2011: 8 publications 2012: 3 publications 2013: 3 publications 2014: 2 publications 2015: 1 publication 2016: 9 publications 2017: 7 publications 2018: 6 publications 2019: 3 publications 2020: 3 publications 2021: 2 publications 2022: 1 publication 2023: 24 publications 2024: 5 publications 2025: 6 publications 2026: 1 publication
1980 2026

277 publications in total across all disciplines

View publications per year as a table
Stuart Schwartz: publications per year, 1980 to 2026
Year Publications
1980 1
1981 0
1982 0
1983 3
1984 2
1985 4
1986 5
1987 1
1988 1
1989 6
1990 5
1991 2
1992 7
1993 10
1994 8
1995 11
1996 11
1997 15
1998 11
1999 14
2000 13
2001 7
2002 11
2003 5
2004 12
2005 8
2006 5
2007 2
2008 8
2009 3
2010 2
2011 8
2012 3
2013 3
2014 2
2015 1
2016 9
2017 7
2018 6
2019 3
2020 3
2021 2
2022 1
2023 24
2024 5
2025 6
2026 1
Total 277
Download as CSV

Stuart Schwartz 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 Stuart Schwartz 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, 225–234 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: 228 publications — 60th percentile

60% 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
205–214 159
215–224 134
225–234 143 228
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
Download as CSV

Stuart Schwartz 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 Stuart Schwartz 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, 70–71 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: 71 D-Index — 51st percentile

51% 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
70–71 158 71
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
Download as CSV

Overview

Stuart Schwartz is affiliated with LabCorp in the United States and has contributed extensively to research in medicine, particularly in the areas of biochemistry, genetics, and molecular biology. Their work encompasses a broad range of topics including prenatal screening and diagnostics, genomic variations and chromosomal abnormalities, genetic syndromes and imprinting, biomedical ethics and regulation, CAR-T cell therapy research, cancer genomics and diagnostics, and chronic myeloid leukemia treatments.

The scientist's recent publications include:

  • Partnering with patients to get better outcomes with chimeric antigen receptor T-cell therapy: towards engagement of patients in early phase trials (2020) - Research Involvement and Engagement
  • Hematologists' barriers and enablers to screening and recruiting patients to a chimeric antigen receptor (CAR) T cell therapy trial: a theory-informed interview study (2021) - Trials
  • Navigating choice in the face of uncertainty: using a theory informed qualitative approach to identifying potential patient barriers and enablers to participating in an early phase chimeric antigen receptor T (CAR-T) cell therapy trial (2021) - BMJ Open
  • Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastoma (2020) - Neuro-Oncology Advances
  • Deletion rescue resulting in segmental homozygosity: A mechanism underlying discordant NIPT results (2020) - American Journal of Medical Genetics Part A

Frequent coauthors collaborating with Stuart Schwartz include:

  • Andrea Penton
  • Gloria Haskell
  • Inder Gadi
  • Alexandra Arreola
  • James Tepperberg

Schwartz has published numerous articles in various scientific journals, with a particular focus on:

  • Genetics in Medicine Open
  • American Journal of Medical Genetics Part A
  • Molecular Cytogenetics
  • Cancer Genetics
  • Research Involvement and Engagement

In terms of fields of study, their work spans across:

  • Medicine
  • Biochemistry, Genetics and Molecular Biology

More specifically, their research delves into subfields such as:

  • Genetics
  • Pediatrics, Perinatology and Child Health
  • Hematology
  • Molecular Biology
  • Physiology

Their research topics cover:

  • Prenatal Screening and Diagnostics
  • Genomic variations and chromosomal abnormalities
  • Genetic Syndromes and Imprinting
  • Biomedical Ethics and Regulation
  • CAR-T cell therapy research
  • Cancer Genomics and Diagnostics
  • Chronic Myeloid Leukemia Treatments

Best Publications

  • Recent Segmental Duplications in the Human Genome

    Jeffrey A. Bailey;Zhiping Gu;Royden A. Clark;Knut Reinert

  • Prader-Willi syndrome

    Suzanne B. Cassidy;Stuart Schwartz;Jennifer L. Miller;Daniel J. Driscoll

  • Segmental Duplications and Copy-Number Variation in the Human Genome

    Andrew J. Sharp;Devin P. Locke;Sean D. McGrath;Ze Cheng

  • Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

    Heather C Mefford;Andrew J Sharp;Carl Baker;Andy Itsara

  • A new human prostate carcinoma cell line, 22Rv1.

    R. Michael Sramkoski;Thomas G. Pretlow;Joseph M. Giaconia;Theresa P. Pretlow

  • Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

    Andrew J Sharp;Sierra Hansen;Rebecca R Selzer;Ze Cheng

  • Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

    Karin Buiting;Shinji Saitoh;Shinji Saitoh;Stephanie Gross;Bärbel Dittrich

  • Evaluation of mental retardation: Recommendations of a consensus conference

    Cynthia J. Curry;Roger E. Stevenson;David Aughton;Janice Byrne

  • The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.

    Meral Gunay-Aygun;Stuart Schwartz;Shauna Heeger;Mary Ann O'Riordan

  • Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome

    Devin P. Locke;Andrew J. Sharp;Steven A. McCarroll;Steven A. McCarroll;Sean D. McGrath

  • CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

    Jose Marcelino;John D. Carpten;Wafaa M. Suwairi;Orlando M. Gutierrez

  • CWR22: The First Human Prostate Cancer Xenograft with Strongly Androgen-dependent and Relapsed Strains Both in Vivo and in Soft Agar

    Moolky Nagabhushan;Casey M. Miller;Theresa P. Pretlow;Joseph M. Giaconia

  • CWR22: Androgen-dependent Xenograft Model Derived from a Primary Human Prostatic Carcinoma

    Mark A. Wainstein;Feng He;Daniel Robinson;Hsing-Jien Kung

  • Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

    Kumar N. Alagramam;Huijun Yuan;Markus H. Kuehn;Crystal L. Murcia

  • Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.

    James M. Amos-Landgraf;Yonggang Ji;Wayne Gottlieb;Theresa Depinet

  • Structure of Chromosomal Duplicons and their Role in Mediating Human Genomic Disorders

    Yonggang Ji;Evan E. Eichler;Stuart Schwartz;Robert D. Nicholls

  • Covariation of synaptonemal complex length and mammalian meiotic exchange rates.

    Audrey Lynn;Kara E. Koehler;LuAnn Judis;Ernest R. Chan

  • Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

    Rachel D. Burnside;Romela Pasion;Fady M. Mikhail;Andrew J. Carroll

  • Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.

    S. B. Cassidy;M. Forsythe;S. Heeger;R. D. Nicholls

  • Identification of centromeric antigens in dicentric Robertsonian translocations: CENP-C and CENP-E are necessary components of functional centromeres

    Beth A. Sullivan;Stuart Schwartz

Frequent Co-Authors

Evan E. Eichler
Evan E. Eichler University of Washington
Robert D. Nicholls
Robert D. Nicholls University of Pittsburgh
Daniel L. Van Dyke
Daniel L. Van Dyke Mayo Clinic
Cynthia C. Morton
Cynthia C. Morton Brigham and Women's Hospital
Urvashi Surti
Urvashi Surti University of Pittsburgh
Terry J. Hassold
Terry J. Hassold Washington State University
Yiping Shen
Yiping Shen Boston Children's Hospital
Andrew J. Sharp
Andrew J. Sharp Icahn School of Medicine at Mount Sinai
Susanne M. Gollin
Susanne M. Gollin University of Pittsburgh
James F. Gusella
James F. Gusella Harvard University

External Links

Personal website of Stuart Schwartz

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Related Online Degrees & Career Pathways

For students passionate about Genetics, numerous online degrees and career pathways in healthcare are available beyond traditional laboratory research. These options can lead to impactful roles in the growing health sector, and many offer flexible, accessible formats for remote learning.

One popular route is pursuing a medical billing and coding course. This field combines knowledge of healthcare systems with expertise in data management and healthcare regulations, making it an excellent fit for those interested in the administrative side of genetics and healthcare.

Aspiring nurses can explore what is the easiest nursing program to get into to find accessible options for starting a clinical career. Nursing skills often complement a background in Genetics, especially in areas like genetic counseling or patient care.

For leadership or organizational roles, consider a health administration degree. These programs prepare students for managing healthcare facilities, programs, or research initiatives and can be earned efficiently through online or accelerated tracks.

Cost is often crucial, and students can explore the cheapest mha programs online for affordable pathways to a master's in healthcare administration. These advanced programs can open doors to executive opportunities in the ever-evolving field of healthcare.

Best Scientists Citing Stuart Schwartz

Evan E. Eichler

Evan E. Eichler

University of Washington

Publications: 242

James R. Lupski

James R. Lupski

Baylor College of Medicine

Publications: 119

Stephen W. Scherer

Stephen W. Scherer

University of Toronto

Publications: 96

Merlin G. Butler

Merlin G. Butler

University of Kansas

Publications: 67

Pawel Stankiewicz

Pawel Stankiewicz

Baylor College of Medicine

Publications: 65

Mariano Rocchi

Mariano Rocchi

University of Bari Aldo Moro

Publications: 54

Karin Buiting

Karin Buiting

University of Duisburg-Essen

Publications: 52

Mario Ventura

Mario Ventura

University of Bari Aldo Moro

Publications: 51

Thomas Liehr

Thomas Liehr

Friedrich Schiller University Jena

Publications: 50

Elaine H. Zackai

Elaine H. Zackai

Children's Hospital of Philadelphia

Publications: 50

Jill A. Rosenfeld

Jill A. Rosenfeld

Baylor College of Medicine

Publications: 50

Charles Lee

Charles Lee

The Jackson Laboratory

Publications: 49

Bernhard Horsthemke

Bernhard Horsthemke

University of Duisburg-Essen

Publications: 48

Lisa G. Shaffer

Lisa G. Shaffer

Paw Print Genetics

Publications: 46

Arthur L. Beaudet

Arthur L. Beaudet

Baylor College of Medicine

Publications: 46

Joris Vermeesch

Joris Vermeesch

KU Leuven

Publications: 41

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Hyuk Lim

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Tim A. Ahles

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Jorma Jokiniemi

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