Robert Marion

979 total citations
25 papers, 611 citations indexed

About

Robert Marion is a scholar working on Molecular Biology, Surgery and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Robert Marion has authored 25 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Surgery and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Robert Marion's work include Congenital heart defects research (6 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Prenatal Screening and Diagnostics (3 papers). Robert Marion is often cited by papers focused on Congenital heart defects research (6 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Prenatal Screening and Diagnostics (3 papers). Robert Marion collaborates with scholars based in United States and United Kingdom. Robert Marion's co-authors include Rosalie Goldberg, Peter Scambler, Paul Saenger, Robert J. Shprintzen, Elaine M. Pereira, K.H. Ramesh, Alan Shanske, Ravelo V. Argamaso, Jane S. Kim and Thomas V. McDonald and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, The Journal of Pediatrics and International Journal of Pharmaceutics.

In The Last Decade

Robert Marion

23 papers receiving 574 citations

Peers

Robert Marion

GENET

PRM

EPIDE

SURGE

D.A. Driscoll United States

Heino Hügel Germany

Amanda L. Bergner United States

Gabrielle J. Halpern Israel

Aline Tamalet France

Margaret Barrow United Kingdom

Heather G. Mack Australia

Mark N. Cruickshank Australia

Christina Zaleski United States

Patricia Robbins‐Furman United States

D.A. Driscoll United States

Robert Marion

338 ×0.9

158 ×0.6

GENET

161 ×0.9

PRM

157 ×0.9

EPIDE

94 ×0.9

SURGE

Citations per year, relative to Robert Marion Robert Marion (= 1×) peers D.A. Driscoll

Countries citing papers authored by Robert Marion

Since Specialization

Citations

This map shows the geographic impact of Robert Marion's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Robert Marion with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Marion more than expected).

Fields of papers citing papers by Robert Marion

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert Marion. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Robert Marion. The network helps show where Robert Marion may publish in the future.

Co-authorship network of co-authors of Robert Marion

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Marion. A scholar is included among the top collaborators of Robert Marion based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Robert Marion. Robert Marion is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Marion, Robert, Thomas V. McDonald, Christine A. Walsh, et al.. (2022). Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner’s office referrals to a multi-disciplinary cardiogenetics program. Journal of Community Genetics. 13(6). 629–639. 8 indexed citations

Marion, Robert, Thomas V. McDonald, Dawei Wang, et al.. (2018). Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case series. Cardiovascular Pathology. 37. 30–33. 7 indexed citations

Massera, Daniele, et al.. (2018). Hyperlipidemia secondary to acitretin therapy for lamellar ichthyosis associated with a NIPAL4 mutation improves on a plant-based diet and relapses on a standard Western diet. Clinical Nutrition ESPEN. 24. 54–57.

McDonald, Thomas V., et al.. (2016). Perceptions of an Implantable Cardioverter-Defibrillator: A Qualitative Study of Families with a History of Sudden, Life-Threatening Cardiac Events, and Recommendations to Improve Care. PubMed. 29(1). 3–3. 4 indexed citations

Gittler, Julia & Robert Marion. (2016). More Than Skin Deep: Genetics, Clinical Manifestations, and Diagnosis of Albinism. 30(1&2). 41–41.

Pereira, Elaine M. & Robert Marion. (2015). Chromosome 22q11.2 Deletion Syndrome. Pediatrics in Review. 36(6). 270–272. 6 indexed citations

Pereira, Elaine M. & Robert Marion. (2015). Chromosome 22q11.2 Deletion Syndrome. Pediatrics in Review. 36(6). 270–272. 1 indexed citations

Ma, Deqiong, Robert Marion, Elaine M. Pereira, et al.. (2014). A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: a novel case report and literature review. Molecular Cytogenetics. 7(1). 85–85. 21 indexed citations

Pereira, Elaine M., et al.. (2012). Hepatoblastoma in a Mosaic Trisomy 18 Patient. Journal of Pediatric Hematology/Oncology. 34(4). e145–e148. 19 indexed citations

10.

Samanich, Joy, et al.. (2012). 17q12 Deletion in a patient with Williams syndrome: Case report and review of the literature.. PubMed. 1(2). 135–41. 2 indexed citations

11.

Marion, Robert, et al.. (2012). Judicial Spectrum Primer: What Judges Need to Know About Children with Autism Spectrum Disorders. Juvenile and Family Court Journal. 63(2). 1–19. 2 indexed citations

12.

Shur, Natasha, Robert Marion, & Susan J. Gross. (2006). A Surprising Postnatal Diagnosis. Obstetrics and Gynecology. 108(1). 189–195. 4 indexed citations

13.

Marion, Robert, et al.. (2005). Sorption of unoprostone isopropyl to packaging materials. International Journal of Pharmaceutics. 307(2). 163–167. 9 indexed citations

14.

Marion, Robert, et al.. (1994). Nasal pyriform aperture stenosis and the holoprosencephaly spectrum. International Journal of Pediatric Otorhinolaryngology. 28(2-3). 199–204. 60 indexed citations

15.

Barone, Constance M., et al.. (1993). Craniofacial, limb, and abdominal anomalies in a distinct syndrome: Relation to the spectrum of Pfeiffer syndrome type 3. American Journal of Medical Genetics. 45(6). 745–750. 13 indexed citations

16.

Marion, Robert, et al.. (1993). Variable phenotypes in velocardiofacial syndrome with chromosomal deletion. The Journal of Pediatrics. 123(3). 406–410. 76 indexed citations

17.

Goldberg, Rosalie, et al.. (1993). Velo‐cardio‐facial syndrome: A review of 120 patients. American Journal of Medical Genetics. 45(3). 313–319. 321 indexed citations

18.

Marion, Robert. (1989). The Intern Blues: The Timeless Classic About the Making of a Doctor. Medical Entomology and Zoology. 1 indexed citations

19.

Marion, Robert. (1980). Communicating with parents of culturally diverse exceptional children.. PubMed. 46(8). 616–23. 39 indexed citations

20.

Chandra, P., et al.. (1979). Experience with sonography as an adjunct to amniocentesis for prenatal diagnosis of fetal genetic disorders. American Journal of Obstetrics and Gynecology. 133(5). 519–524. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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