World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
86
Citations
24539
World Ranking
2999
National Ranking
1530

Medicine

D-Index
89
Citations
28167
World Ranking
12723
National Ranking
6505

Research.com Recognitions

  • 1955 - Fellow of the American Association for the Advancement of Science (AAAS)

Overview

John M. Graham is affiliated with Cedars-Sinai Medical Center in the United States. Their research spans multiple disciplines within medicine and biochemistry, genetics, and molecular biology. The primary fields of study include Medicine with 129 publications and Biochemistry, Genetics and Molecular Biology with 123 publications. Their work extends to several subfields: Genetics, Surgery, Molecular Biology, Pediatrics, Perinatology and Child Health, and Epidemiology.

Key research topics covered by John M. Graham include:

  • Craniofacial Disorders and Treatments
  • Cleft Lip and Palate Research
  • Genomics and Rare Diseases
  • Genetics and Neurodevelopmental Disorders
  • Genomic Variations and Chromosomal Abnormalities
  • Neurogenetic and Muscular Disorders Research
  • Congenital Heart Defects Research

The scientist has authored and co-authored multiple papers reflecting their involvement in diverse topics. Notable recent publications are:

  • "Update on the gestational effects of maternal hyperthermia," 2020, Birth Defects Research
  • "A dyadic approach to the delineation of diagnostic entities in clinical genomics," 2021, The American Journal of Human Genetics
  • "Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome," 2021, American Journal of Medical Genetics Part A
  • "A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statement," 2021, Clinical Genetics
  • "Canadian Spontaneous Coronary Artery Dissection Cohort Study," 2022, Journal of the American College of Cardiology

Frequent co-authors who have collaborated on numerous publications with John M. Graham include:

  • Pedro A. Sanchez-Lara
  • Katheryn Grand
  • Fowzan S. Alkuraya
  • Cynthia J. Curry
  • Margaret P Adam

The scientist has contributed to book publications with Garland Science eBooks, including "Biological Centrifugation" (2020) and "Membrane Analysis" (2020).

John M. Graham's work has appeared frequently in several publication venues, notably:

  • American Journal of Medical Genetics Part A
  • UNC Libraries
  • American Journal of Medical Genetics Part C Seminars in Medical Genetics
  • The American Journal of Human Genetics
  • arXiv (Cornell University)

Throughout their career, John M. Graham received recognition including being named a Fellow of the American Association for the Advancement of Science (AAAS) in 1955.

Best Publications

  • Incidence of fetal alcohol syndrome and prevalence of alcohol-related neurodevelopmental disorder

    Paul D. Sampson;Ann P. Streissguth;Fred L. Bookstein;Ruth E. Little

  • Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association.

    Roberta A. Pagon;John M. Graham;Jonathan Zonana;Siu Li Yong

  • De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

    Jean Baptiste Rivière;Ghayda M. Mirzaa;Brian J. O'Roak;Margaret Beddaoui

  • GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.

    Seongman Kang;John M. Graham;Ann Haskins Olney;Leslie G. Biesecker

  • Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.

    J. H. M. Knoll;J. H. M. Knoll;R. D. Nicholls;R. D. Nicholls;R. E. Magenis;J. M. Graham

  • PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome

    Debbie J. Marsh;Debbie J. Marsh;Jennifer B. Kum;Jennifer B. Kum;Kathryn L. Lunetta;Michael J. Bennett

  • Evaluation of mental retardation: Recommendations of a consensus conference

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

  • CHARGE Association: An Update and Review for the Primary Pediatrician

    Kim D. Blake;Sandra L. H. Davenport;Bryan D. Hall;Margaret A. Hefner

  • Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation.

    Leslie G. Biesecker;Rudolf Happle;John B. Mulliken;Rosanna Weksberg

  • Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation

    Seema R. Lalani;Arsalan M. Safiullah;Susan D. Fernbach;Karine C. Harutyunyan

  • Klinefelter syndrome and other sex chromosomal aneuploidies

    Jeannie Visootsak;John M Graham

  • An epidemiological analysis of CHARGE syndrome: preliminary results from a Canadian study.

    Karina A. Issekutz;John M. Graham;Chitra Prasad;Isabel M. Smith

  • Molar Tooth Sign of the Midbrain-Hindbrain Junction: Occurrence in Multiple Distinct Syndromes

    Joseph G. Gleeson;Lesley C. Keeler;Melissa A. Parisi;Sarah E. Marsh

  • Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis

    Deborah Krakow;Deborah Krakow;Stephen P Robertson;Lily M King;Timothy Morgan

  • Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

    Jennifer J. Johnston;Isabelle Olivos-Glander;Christina Killoran;Emma Elson

  • Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum.

    Kim M Keppler-Noreuil;Julie C Sapp;Marjorie J Lindhurst;Victoria Er Parker

  • Teratogen update: gestational effects of maternal hyperthermia due to febrile illnesses and resultant patterns of defects in humans.

    John M. Graham;Matthew J. Edwards;Marshall J. Edwards

  • Management of deformational plagiocephaly: Repositioning versus orthotic therapy

    John M. Graham;Mayela Gomez;Andy Halberg;Dawn L. Earl

  • Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis.

    Ghayda M. Mirzaa;Robert L. Conway;Karen W. Gripp;Tally Lerman-Sagie

  • Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

    Irene A Aligianis;Colin A Johnson;Paul Gissen;Dongrong Chen

Frequent Co-Authors

David L. Rimoin
David L. Rimoin Cedars-Sinai Medical Center
Ralph S. Lachman
Ralph S. Lachman University of California, Los Angeles
William B. Dobyns
William B. Dobyns University of Minnesota
Leslie G. Biesecker
Leslie G. Biesecker National Institutes of Health
Elaine H. Zackai
Elaine H. Zackai Children's Hospital of Philadelphia
Roger E. Stevenson
Roger E. Stevenson Clemson University
Peter Brugger
Peter Brugger University of Zurich
Charles E. Schwartz
Charles E. Schwartz Greenwood Genetic Center
William R. Wilcox
William R. Wilcox Emory University
Deborah Krakow
Deborah Krakow University of California, Los Angeles

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