Marybeth Hummel

2.5k total citations
23 papers, 482 citations indexed

About

Marybeth Hummel is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marybeth Hummel has authored 23 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marybeth Hummel's work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers) and Prenatal Screening and Diagnostics (5 papers). Marybeth Hummel is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers) and Prenatal Screening and Diagnostics (5 papers). Marybeth Hummel collaborates with scholars based in United States, United Kingdom and Germany. Marybeth Hummel's co-authors include Sharon L. Wenger, John Powell, Sarah Curran, Frances Elmslie, Ajay Sharma, Aaron R. Jeffries, V. Reid Sutton, Ankita Patel, Jonathan S. Berg and Seema R. Lalani and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Investigative Ophthalmology & Visual Science.

In The Last Decade

Marybeth Hummel

23 papers receiving 467 citations

Peers

Marybeth Hummel

GENET

SURGE

PPCH

EPIDE

Fortunato Lonardo Italy

Shihui Yu China

Constance K. Stein United States

Elisa Tassano Italy

Anita Wischmeijer Italy

Anne Destrèe Belgium

Karen J. Harrison Canada

Axel Bohring Germany

Nicolas Gruchy France

Frank X. Donovan United States

Fortunato Lonardo Italy

Marybeth Hummel

350 ×1.2

GENET

258 ×0.9

73 ×1.0

SURGE

99 ×1.8

PPCH

36 ×0.7

EPIDE

Citations per year, relative to Marybeth Hummel Marybeth Hummel (= 1×) peers Fortunato Lonardo

Countries citing papers authored by Marybeth Hummel

Since Specialization

Citations

This map shows the geographic impact of Marybeth Hummel'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 Marybeth Hummel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marybeth Hummel more than expected).

Fields of papers citing papers by Marybeth Hummel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marybeth Hummel. 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 Marybeth Hummel. The network helps show where Marybeth Hummel may publish in the future.

Co-authorship network of co-authors of Marybeth Hummel

This figure shows the co-authorship network connecting the top 25 collaborators of Marybeth Hummel. A scholar is included among the top collaborators of Marybeth Hummel 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 Marybeth Hummel. Marybeth Hummel 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

Küstner, E, Marybeth Hummel, Thomas Kubiak, et al.. (2018). Ältere Menschen mit Diabetes mellitus Typ 1 und CSII Gibt es Unterschiede im Vergleich zur ICT? Analyse des DPV-Registers. Diabetologie und Stoffwechsel. 1 indexed citations

Ba‐Abbad, Rola, Monique Leys, Xinjing Wang, et al.. (2018). Clinical Features of a Retinopathy Associated With a Dominant Allele of the RGR Gene. Investigative Ophthalmology & Visual Science. 59(12). 4812–4812. 10 indexed citations

Leys, Monique, Marybeth Hummel, Alexandra V. Garafalo, et al.. (2014). RGR gene mutation causative of peripapillary choroidal atrophy. Investigative Ophthalmology & Visual Science. 55(13). 1242–1242. 2 indexed citations

Hummel, Marybeth, et al.. (2011). Fahrerassistenzsysteme. Ermittlung des Sicherheitspotenzials auf Basis des Schadengeschehens der Deutschen Versicherer. 6 indexed citations

Karnsakul, Wikrom, et al.. (2010). Obesity and Reversed Growth Retardation in a Child with Type Ia Glycogen Storage Disease. Journal of Pediatric Endocrinology and Metabolism. 23(5). 507–12. 4 indexed citations

Bailey, Nathanael G., Sarah T. South, Marybeth Hummel, & Sharon L. Wenger. (2010). Case report: cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with wolf-hirschhorn syndrome.. PubMed. 36(1). 5–10. 6 indexed citations

Dod, Harvinder S., et al.. (2009). Left ventricular noncompaction: A rare disorder in adults and its association with 1p36 chromosomal anomaly. American Journal of Medical Genetics Part A. 152A(1). 191–195. 6 indexed citations

Ben‐Shachar, Shay, Zhishuo Ou, Chad A. Shaw, et al.. (2008). 22q11.2 Distal Deletion: A Recurrent Genomic Disorder Distinct from DiGeorge Syndrome and Velocardiofacial Syndrome. The American Journal of Human Genetics. 82(1). 214–221. 142 indexed citations

Schneider, Adele, Tanya Bardakjian, Jie Zhou, et al.. (2008). Familial recurrence of SOX2 anophthalmia syndrome: Phenotypically normal mother with two affected daughters. American Journal of Medical Genetics Part A. 146A(21). 2794–2798. 24 indexed citations

10.

Hummel, Marybeth, et al.. (2007). Novel CDH3 mutations in hypotrichosis with juvenile macular dystrophy. Clinical and Experimental Dermatology. 32(2). 191–196. 26 indexed citations

11.

Wenger, Sharon L., Paul Grossfeld, Benjamin L. Siu, et al.. (2006). Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome. American Journal of Medical Genetics Part A. 140A(7). 704–708. 22 indexed citations

12.

Yu, Min, et al.. (2005). Prenatal detection of deletion 6q13q15 in a complex karyotype. Prenatal Diagnosis. 25(12). 1084–1087. 7 indexed citations

13.

Jeffries, Aaron R., Sarah Curran, Frances Elmslie, et al.. (2005). Molecular and phenotypic characterization of ring chromosome 22. American Journal of Medical Genetics Part A. 137A(2). 139–147. 85 indexed citations

14.

Siu, Benjamin L., et al.. (2004). Mosaic ring 12p and total anomalous pulmonary venous return. American Journal of Medical Genetics Part A. 131A(1). 91–93. 7 indexed citations

15.

Wenger, Sharon L., et al.. (2004). Cleft Palate in a Newborn with Duplication 2(q13q23). The Cleft Palate-Craniofacial Journal. 41(5). 568–570. 3 indexed citations

16.

Hummel, Marybeth, David Cunningham, Charles J. Mullett, Richard I. Kelley, & Gail E. Herman. (2003). Left‐sided CHILD syndrome caused by a nonsense mutation in the NSDHL gene. American Journal of Medical Genetics Part A. 122A(3). 246–251. 32 indexed citations

17.

Hummel, Marybeth, et al.. (2002). Trisomy 8 mosaicism: Selective growth advantage of normal cells vs. growth disadvantage of trisomy 8 cells. American Journal of Medical Genetics Part A. 116A(2). 144–146. 11 indexed citations

18.

Wenger, Sharon L., et al.. (2000). Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s. American Journal of Medical Genetics. 91(5). 351–354. 9 indexed citations

19.

Hummel, Marybeth, et al.. (1999). Hypoplastic external genitalia in association with X;autosome chromosome translocation. Journal of Pediatric and Adolescent Gynecology. 12(3). 161–164. 7 indexed citations

20.

Hummel, Marybeth, et al.. (1995). Association of kyphomelic dysplasia with severe combined immunodeficiency. American Journal of Medical Genetics. 57(4). 626–629. 18 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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