World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
71
Citations
21335
World Ranking
2174
National Ranking
986

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
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

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