Catherine A. Stolle

3.4k total citations
60 papers, 2.2k citations indexed

About

Catherine A. Stolle is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Catherine A. Stolle has authored 60 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 23 papers in Genetics and 17 papers in Cancer Research. Recurrent topics in Catherine A. Stolle's work include Connective tissue disorders research (14 papers), Cancer, Hypoxia, and Metabolism (14 papers) and Craniofacial Disorders and Treatments (9 papers). Catherine A. Stolle is often cited by papers focused on Connective tissue disorders research (14 papers), Cancer, Hypoxia, and Metabolism (14 papers) and Craniofacial Disorders and Treatments (9 papers). Catherine A. Stolle collaborates with scholars based in United States, Canada and Japan. Catherine A. Stolle's co-authors include W. Marston Linehan, Berton Zbar, Elaine H. Zackai, Karen W. Gripp, G.M. Glenn, Peter L. Choyke, Darwin J. Prockop, Jeffrey S. Humphrey, Richard D. Klausner and Jeanne C. Myers and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Catherine A. Stolle

60 papers receiving 2.2k citations

Peers

Countries citing papers authored by Catherine A. Stolle

Since Specialization

Citations

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

Fields of papers citing papers by Catherine A. Stolle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine A. Stolle. 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 Catherine A. Stolle. The network helps show where Catherine A. Stolle may publish in the future.

Co-authorship network of co-authors of Catherine A. Stolle

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	An Expanded Role for HLA Genes: HLA-B Encodes a microRNA that Regulates IgA and Other Immune Response Transcripts 2017 ·Frontiers in Immunology ·Nilesh Chitnis, Peter Clark, Malek Kamoun, Catherine A. Stolle, F. Brad Johnson, Dimitri Monos	29
2	Mung Bean Nuclease Treatment Increases Capture Specificity of Microdroplet-PCR Based Targeted DNA Enrichment 2014 ·PLoS ONE ·Zhenming Yu, Kajia Cao, (unknown), Catherine A. Stolle, Avni Santani	1
3	A Hemoglobin Variant Associated with Neonatal Cyanosis and Anemia 2011 ·New England Journal of Medicine ·Moira Crowley, Todd L. Mollan, Osheiza Abdulmalik, (unknown), (unknown), Arindam Sarkar, Catherine A. Stolle, Andrew J. Gow, John S. Olson, Mitchell J. Weiss	19
4	Clinical and functional properties of novel VHL mutation (X214L) consistent with Type 2A phenotype and low risk of renal cell carcinoma 2010 ·Clinical Genetics ·(unknown), (unknown), Catherine A. Stolle, Joshua D.I. Ellenhorn, Arthur Grix, (unknown), Jeffrey N. Weitzel	9
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	Detection of germline deletions using real‐time quantitative polymerase chain reaction in Japanese patients with von Hippel–Lindau disease 2006 ·Cancer Science ·Kéiko Hattori, Jun‐ichi Teranishi, Catherine A. Stolle, Minoru Yoshida, Keiichi Kondo, Takeshi Kishida, Hiroshi Kanno, Masaya Baba, Yoshinobu Kubota, Masahiro Yao	20
7	EARLY ONSET HEREDITARY PAPILLARY RENAL CARCINOMA: GERMLINE MISSENSE MUTATIONS IN THE TYROSINE KINASE DOMAIN OF THE MET PROTO-ONCOGENE 2004 ·The Journal of Urology ·Laura S. Schmidt, Michael L. Nickerson, Debora Angeloni, G.M. Glenn, McClellan M. Walther, Paul S. Albert, Michelle B. Warren, Peter L. Choyke, Carlos A. Torres‐Cabala, Maria J. Merino, Joan Brunet, (unknown), Joan Borràs, (unknown), Lindsay Middelton, John L. Phillips, Catherine A. Stolle, Berton Zbar, Stephen E. Pautler, W. Marston Linehan	75
8	Molecular characterization of Pfeiffer syndrome: Implications for prognosis and genetic counseling. 2003 ·The American Journal of Human Genetics ·Donna M. McDonald‐McGinn, Ralph J. DeBerardinis, Sean Bartlett, Linda Whitaker, Ian Jacobs, Karen W. Gripp, Catherine A. Stolle, (unknown), Maximilian Muenke, E H Zackai	1
9	Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma 2002 ·Oncogene ·Christian A. Koch, Steve Huang, Zhengping Zhuang, Catherine A. Stolle, Norio Azumi, George P. Chrousos, Alexander O. Vortmeyer, Karel Pacák	29
10	Childhood cerebellar hemangioblastoma does not predict germline or somatic mutations in the von Hippel‐Lindau tumor suppressor gene 2002 ·Annals of Neurology ·Paul G. Fisher, (unknown), (unknown), Patricia K. Duffner, Douglas J. Hyder, Catherine A. Stolle, Alexander O. Vortmeyer, Zhengping Zhuang	10
11	A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: Fluorescence in situ hybridization and dosage-sensitive Southern blot analysis 2001 ·Genetics in Medicine ·Karen W. Gripp, Viera Kasparcova, Donna M. McDonald‐McGinn, Sucheta Bhatt, Scott P. Bartlett, Andrea L. Storm, Timothy Drumheller, Beverly S. Emanuel, Elaine H. Zackai, Catherine A. Stolle	13
12	Mosaicism in von Hippel–Lindau Disease: Lessons from Kindreds with Germline Mutations Identified in Offspring with Mosaic Parents 2000 ·The American Journal of Human Genetics ·Maria Sgambati, Catherine A. Stolle, Peter L. Choyke, (unknown), Berton Zbar, W. Marston Linehan, G.M. Glenn	122
13	Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization. 1999 ·PubMed ·Svetlana Pack, Berton Zbar, Evgenia Pak, (unknown), Jeffrey S. Humphrey, (unknown), (unknown), Robert J. Weil, (unknown), Igor Kuzmin, Catherine A. Stolle, G.M. Glenn, Luigi Liotta, Michael I. Lerman, Richard D. Klausner, W. Marston Linehan, Zhengping Zhuang	47
14	A New Twist: Some Patients with Saethre-Chotzen Syndrome Have a Microdeletion Syndrome 1998 ·The American Journal of Human Genetics ·Elaine H. Zackai, Catherine A. Stolle	15
15	Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene 1998 ·Human Mutation ·Catherine A. Stolle, G.M. Glenn, Berton Zbar, Jeffrey S. Humphrey, Peter L. Choyke, McClellan M. Walther, (unknown), Kathy Hurley, (unknown), Richard D. Klausner, W. Marston Linehan	346
16	Multiple Defects in Type III Collagen Synthesis Are Associated with the Pathogenesis of Abdominal Aortic Aneurysmsa 1996 ·Annals of the New York Academy of Sciences ·David W. Anderson, (unknown), Michael Ricketts, Helena Kuivaniemi, Gerard Tromp, Catherine A. Stolle, Susan B. Deak, Charles D. Boyd	34
17	Phenotypic Overlap between Familial Aneurysms and Ehlers‐Danlos Syndrome Type IV Resulting from a Type III Procollagen Gene Mutation 1996 ·Annals of the New York Academy of Sciences ·David W. Anderson, Smita Thakker‐Varia, Catherine A. Stolle	3
18	Aberrant splicing of the type III procollagen mRNA leads to intracellular degradation of the protein in a patient with ehlers-danlos type IV 1995 ·Human Mutation ·Smita Thakker‐Varia, David W. Anderson, Helena Kuivaniemi, Gerard Tromp, (unknown), Michel van der Rest, Francis H. Glorieux, Leena Ala-Kokko, Catherine A. Stolle	10
19	Alternative Splicing of Rat Tropoelastin mRNA is Tissue-Specific and Developmentally Regulated 1991 ·Matrix ·Ruth A. Heim, Richard A. Pierce, Susan B. Deak, D. Riley, Charles D. Boyd, Catherine A. Stolle	32
20	Heterogeneity of rat tropoelastin mRNA revealed by cDNA cloning 1990 ·Biochemistry ·Richard A. Pierce, Susan B. Deak, Catherine A. Stolle, Charles D. Boyd	64

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.

Explore authors with similar magnitude of impact