Robert W. Marion

2.3k total citations
47 papers, 1.2k citations indexed

About

Robert W. Marion is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Robert W. Marion has authored 47 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Robert W. Marion's work include Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (8 papers) and Connective tissue disorders research (6 papers). Robert W. Marion is often cited by papers focused on Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (8 papers) and Connective tissue disorders research (6 papers). Robert W. Marion collaborates with scholars based in United States, Canada and Netherlands. Robert W. Marion's co-authors include Alan Shanske, John M. Opitz, Susann Schweiger, Grazia Andolfi, George Feldman, Nandita Quaderi, Brunella Franco, Hilger H. Ropers, Andrea Ballabio and Raoul C. M. Hennekam and has published in prestigious journals such as JAMA, Nature Genetics and PLoS ONE.

In The Last Decade

Robert W. Marion

43 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Robert W. Marion United States 19 520 460 138 120 111 47 1.2k
Usha Kini India 21 485 0.9× 382 0.8× 195 1.4× 90 0.8× 472 4.3× 99 1.5k
Marie Legendre France 23 741 1.4× 583 1.3× 143 1.0× 104 0.9× 97 0.9× 82 1.6k
Carlo Marcelis Netherlands 25 757 1.5× 433 0.9× 327 2.4× 121 1.0× 93 0.8× 67 1.6k
Jasper J. van der Smagt Netherlands 22 623 1.2× 483 1.1× 113 0.8× 59 0.5× 130 1.2× 48 1.5k
David George United States 20 697 1.3× 119 0.3× 94 0.7× 166 1.4× 50 0.5× 28 1.2k
G. Shashidhar Pai United States 25 796 1.5× 981 2.1× 232 1.7× 61 0.5× 450 4.1× 55 1.9k
Daniel Pietryga United States 14 817 1.6× 178 0.4× 109 0.8× 306 2.5× 195 1.8× 22 2.1k
Meinhard Robinow United States 21 781 1.5× 599 1.3× 243 1.8× 118 1.0× 229 2.1× 70 1.7k
Dagan A. Loisel United States 11 392 0.8× 304 0.7× 47 0.3× 45 0.4× 53 0.5× 14 1.2k
Sabine Sigaudy France 21 629 1.2× 535 1.2× 205 1.5× 62 0.5× 220 2.0× 70 1.3k

Countries citing papers authored by Robert W. Marion

Since Specialization
Citations

This map shows the geographic impact of Robert W. 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 W. 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 W. Marion more than expected).

Fields of papers citing papers by Robert W. Marion

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert W. 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 W. Marion. The network helps show where Robert W. Marion may publish in the future.

Co-authorship network of co-authors of Robert W. Marion

This figure shows the co-authorship network connecting the top 25 collaborators of Robert W. Marion. A scholar is included among the top collaborators of Robert W. 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 W. Marion. Robert W. Marion is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Marion, Robert W., et al.. (2021). Caregiver‐reported characteristics of children diagnosed with pathogenic variants in KDM5C . American Journal of Medical Genetics Part A. 185(10). 2951–2958. 6 indexed citations
2.
Silverstein, Louise B., Thomas V. McDonald, Christine A. Walsh, et al.. (2014). Psychological Stress Associated with Cardiogenetic Conditions. Personalized Medicine. 11(7). 631–640. 11 indexed citations
3.
Wang, Tao, Joy Samanich, Chad Haldeman‐Englert, et al.. (2013). Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams–Beuren syndrome. American Journal of Medical Genetics Part A. 161(3). 527–533. 19 indexed citations
4.
Shanske, Alan, et al.. (2005). Prenatal Diagnosis of Marshall Syndrome by Targeted Sonography. Journal of Ultrasound in Medicine. 24(12). 1735–1737.
5.
Dolan, Siobhan M., Alan Shanske, Robert W. Marion, & Susan J. Gross. (2003). First‐trimester diagnosis of Bartsocas–Papas syndrome (BPS) by transvaginal ultrasound: case report and review of the literature. Prenatal Diagnosis. 23(2). 138–142. 11 indexed citations
6.
Goodrich, James T., et al.. (2000). Fronto-Ocular syndrome: Newly recognized trigonocephaly syndrome. American Journal of Medical Genetics. 93(2). 89–93. 5 indexed citations
7.
Ferreira, José Carlos, Peter S. Bernstein, Ethylin Wang Jabs, et al.. (1999). Second‐trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findings. Ultrasound in Obstetrics and Gynecology. 14(6). 426–430. 34 indexed citations
8.
Huie, Maryann L., Alan Shanske, Jocelyn S. Kasper, Robert W. Marion, & Rochelle Hirschhorn. (1999). A large Alu -mediated deletion, identified by PCR, as the molecular basis for glycogen storage disease Type II (GSDII). Human Genetics. 104(1). 94–98. 20 indexed citations
9.
Robin, Nathaniel H., Jennifer A. Scott, James E. Arnold, et al.. (1998). Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: Implications for classification. American Journal of Medical Genetics. 75(3). 240–244. 1 indexed citations
10.
Shanske, Alan, et al.. (1997). The Marshall syndrome: Report of a new family and review of the literature. American Journal of Medical Genetics. 70(1). 52–57. 21 indexed citations
11.
Marion, Robert W., et al.. (1997). Hemimaxillofacial dysplasia. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 83(4). 484–488. 22 indexed citations
12.
Quaderi, Nandita, Susann Schweiger, Karin Gaudenz, et al.. (1997). Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nature Genetics. 17(3). 285–291. 283 indexed citations
13.
Marion, Robert W.. (1996). The Christmas present. American Journal of Medical Genetics. 66(3). 247–249.
14.
Glickstein, Julie S., et al.. (1995). “C” Trigonocephaly syndrome: Report of a child with agenesis of the corpus callosum and tetralogy of Fallot, and review. American Journal of Medical Genetics. 56(2). 215–218. 10 indexed citations
15.
Marion, Robert W., et al.. (1993). Apparent dominant transmission of the Rubinstein‐Taybi syndrome. American Journal of Medical Genetics. 46(3). 284–287. 25 indexed citations
16.
Marion, Robert W.. (1991). The Genetic Anatomy of Hearing. Annals of the New York Academy of Sciences. 630(1). 32–37. 4 indexed citations
17.
Conway, Edward E., Jacqueline A. Noonan, Robert W. Marion, & Carl N. Steeg. (1990). Myocardial infarction leading to sudden death in the Williams syndrome: Report of three cases. The Journal of Pediatrics. 117(4). 593–595. 54 indexed citations
18.
19.
Singer, Lewis P., et al.. (1989). Limb deficiency in an infant with Smith‐Lemli‐Opitz syndrome. American Journal of Medical Genetics. 32(3). 380–383. 12 indexed citations
20.
Chitayat, David, Sachiko Nakagawa, Robert W. Marion, et al.. (1988). Aspartylglucosaminuria in a Puerto Rican family: Additional features of a panethnic disorder. American Journal of Medical Genetics. 31(3). 527–532. 11 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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