• 2274 Citations
  • 22 h-Index
1979 …2019
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Fingerprint Dive into the research topics where Robert W. Marion is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
DiGeorge Syndrome Medicine & Life Sciences
Prenatal Diagnosis Medicine & Life Sciences
Genetic Drift Medicine & Life Sciences
Acrocephalosyndactylia Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genetic Counseling Medicine & Life Sciences
Williams Syndrome Medicine & Life Sciences
Physician-Patient Relations Medicine & Life Sciences

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Publications 1979 2019

  • 2274 Citations
  • 22 h-Index
  • 100 Article
  • 2 Chapter
  • 1 Comment/debate
  • 1 Letter

Corrigendum to: An Interdomain KCNH2 Mutation Produces an Intermediate Long QT Syndrome (Human Mutation, (2015), 36, 8, (764-773), 10.1002/humu.22805)

Osterbur, M. L., Zheng, R., Marion, R., Walsh, C. & McDonald, T. V., Mar 1 2019, In : Human Mutation. 40, 3, 1 p.

Research output: Contribution to journalComment/debate

Open Access
Long QT Syndrome

Contiguous gene syndromes

Pereira, E. & Marion, R. W., Jan 1 2018, In : Pediatrics in Review. 39, 1, p. 46-48 3 p.

Research output: Contribution to journalArticle

Lamellar Ichthyosis
3 Citations (Scopus)

Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case series

Williams, N., Marion, R. W., McDonald, T. V., Wang, D., Zhou, B., Eng, L. S., Um, S. Y., Lin, Y., Ruiter, K., Rojas, L., Sampson, B. A. & Tang, Y., Nov 1 2018, In : Cardiovascular Pathology. 37, p. 30-33 4 p.

Research output: Contribution to journalArticle

Carrier Proteins
Protein C
Hypertrophic Cardiomyopathy


Levy, P. A. & Marion, R. W., Feb 1 2018, In : Pediatrics in Review. 39, 2, p. 104-106 3 p.

Research output: Contribution to journalArticle