Debra L. Collins

1.5k total citations
17 papers, 487 citations indexed

About

Debra L. Collins is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Debra L. Collins has authored 17 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Debra L. Collins's work include Cancer, Hypoxia, and Metabolism (4 papers), Epigenetics and DNA Methylation (2 papers) and Genetic factors in colorectal cancer (2 papers). Debra L. Collins is often cited by papers focused on Cancer, Hypoxia, and Metabolism (4 papers), Epigenetics and DNA Methylation (2 papers) and Genetic factors in colorectal cancer (2 papers). Debra L. Collins collaborates with scholars based in United States, Germany and Canada. Debra L. Collins's co-authors include R. Neil Schimke, Lawrence M. Gelbert, James M. Lamiell, Jean M. Whaley, Hartmut P.H. Neumann, Y. Edward Hsia, Catherine A. Stolle, Joseph G. Naglich, William A. Horton and John M. Opitz and has published in prestigious journals such as The American Journal of Gastroenterology, Clinical Gastroenterology and Hepatology and Urology.

In The Last Decade

Debra L. Collins

17 papers receiving 476 citations

Peers

Countries citing papers authored by Debra L. Collins

Since Specialization

Citations

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

Fields of papers citing papers by Debra L. Collins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Debra L. Collins. 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 Debra L. Collins. The network helps show where Debra L. Collins may publish in the future.

Co-authorship network of co-authors of Debra L. Collins

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Colorectal Neoplasia in CDH1 Pathogenic Variant Carriers: A Multicenter Analysis 2022 ·The American Journal of Gastroenterology ·Peter P. Stanich, (unknown), Elena M. Stoffel, Erika Koeppe, Ajay Bansal, (unknown), Debra L. Collins, Dana Clark, (unknown), Beth Dudley, Randall E. Brand, Michael J. Hall, (unknown), Brian A. Sullivan, Charles Muller, Alice Hinton, Bryson W. Katona, Sonia S. Kupfer	2
2	Schimke XLID syndrome results from a deletion in BCAP31 2020 ·American Journal of Medical Genetics Part A ·Raymond J. Louie, Debra L. Collins, Michael J. Friez, Cindy Skinner, Charles E. Schwartz, Roger E. Stevenson	7
3	Preoperative Screening of Colorectal Cancers Is As Accurate As Postoperative Screening for Detection of Lynch Syndrome 2020 ·Clinical Gastroenterology and Hepatology ·(unknown), (unknown), (unknown), Daniel Buckles, Anwaar Saeed, Kevin Kennedy, Debra L. Collins, Mojtaba Olyaee, Rashna Madan, Ajay Bansal	2
4	Hereditary cancer screening: Case reports and review of literature on ten Ashkenazi Jewish founder mutations 2018 ·Molecular Genetics & Genomic Medicine ·Devin M. Cox, Katherine Nelson, (unknown), Debra L. Collins	10
5	Paraganglioma, neuroblastoma, and a SDHB mutation: Resolution of a 30‐year‐old mystery 2010 ·American Journal of Medical Genetics Part A ·R. Neil Schimke, Debra L. Collins, Catherine A. Stolle	58
6	The Hunter–MacDonald syndrome with expanded phenotype including risk of meningioma: An update and review 2007 ·American Journal of Medical Genetics Part A ·Linlea Armstrong, Gail E. Graham, R. Neil Schimke, Debra L. Collins, Daniel J. Kirse, Fiona Costello, Holly H Ardinger	2
7	Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene 1999 ·American Journal of Medical Genetics ·J. F. N. Bradley, Debra L. Collins, R. Neil Schimke, (unknown), Paul G. Rothberg	24
8	Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma. 1994 ·PubMed ·Jean M. Whaley, Joseph G. Naglich, Lawrence M. Gelbert, Y. Edward Hsia, James M. Lamiell, (unknown), Debra L. Collins, Hartmut P.H. Neumann, (unknown), (unknown)	192
9	Congenital nonprogressive myopathy with Möbius and Robin sequence—the Carey‐Fineman‐Ziter syndrome: A confirmatory report 1993 ·American Journal of Medical Genetics ·R. Neil Schimke, Debra L. Collins, John M. Hiebert	14
10	Proximal 3p deletion in renal cell carcinoma cells from a patient with von Hippel-Lindau disease 1987 ·Cancer Genetics and Cytogenetics ·Charles R. King, R. Neil Schimke, (unknown), (unknown), Debra L. Collins	46
11	Nasopharyngeal carcinoma, aplastic anemia, and various malignancies in a family: Possible role of Epstein‐Barr virus 1987 ·American Journal of Medical Genetics ·R. Neil Schimke, Debra L. Collins, (unknown), John M. Opitz, James F. Reynolds	11
12	A new X‐linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness 1984 ·American Journal of Medical Genetics ·R. Neil Schimke, William A. Horton, Debra L. Collins, (unknown), John M. Opitz	25
13	Diagnosis and management of asymptomatic renal cell carcinomas in von Hippel-Lindau syndrome 1983 ·Urology ·Errol Levine, John W. Weigel, Debra L. Collins	25
14	Brachyolmia, recessive type (Hobaek): A clinical, radiographic, and histochemical study 1983 ·American Journal of Medical Genetics ·William A. Horton, Leonard O. Langer, Debra L. Collins, (unknown)	19
15	Discordance for the Kleeblattschädel anomaly in monozygotic twins with thanatophoric dysplasia 1983 ·American Journal of Medical Genetics ·William A. Horton, David J. Harris, Debra L. Collins, John M. Opitz	17
16	Moebius syndrome in a child and extremity defect in her father 1982 ·Clinical Genetics ·Debra L. Collins, R. Neil Schimke	15
17	Familial joint instability syndrome 1980 ·American Journal of Medical Genetics ·William A. Horton, Debra L. Collins, Arthur A. DeSmet, James A. Kennedy, R. Neil Schimke, John M. Opitz	18

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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