Catherine Phelan

4.8k total citations
28 papers, 1.0k citations indexed

About

Catherine Phelan is a scholar working on Molecular Biology, Genetics and Materials Chemistry. According to data from OpenAlex, Catherine Phelan has authored 28 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Materials Chemistry. Recurrent topics in Catherine Phelan's work include BRCA gene mutations in cancer (7 papers), Advanced biosensing and bioanalysis techniques (7 papers) and Quantum Dots Synthesis And Properties (5 papers). Catherine Phelan is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Advanced biosensing and bioanalysis techniques (7 papers) and Quantum Dots Synthesis And Properties (5 papers). Catherine Phelan collaborates with scholars based in United States, Canada and Sweden. Catherine Phelan's co-authors include Steven A. Narod, Norman P. Gerry, Joseph Day, Francis Barany, Reyna Favis, Catharina Larsson, Thomas A. Sellers, Ganna Chornokur, Susan T. Vadaparampil and Victoria Sopik and has published in prestigious journals such as Applied Physics Letters, Nature Biotechnology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Catherine Phelan

28 papers receiving 1.0k citations

Peers

Countries citing papers authored by Catherine Phelan

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Phelan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Phelan

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

#	Work	Indexed citations
1	miRNAs associated with prostate cancer risk and progression 2017 ·BMC Urology ·Hung N. Luu, Hui‐Yi Lin, Karina D. Sørensen, Olorunseun O. Ogunwobi, Nagi B. Kumar, Ganna Chornokur, Catherine Phelan, (unknown), LaCreis R. Kidd, Jyotsna Batra, Kosj Yamoah, Anders Berglund, Robert J. Rounbehler, Mihi Yang, Sang Haak Lee, Nahyeon Kang, Seung Joon Kim, Jong Y. Park, Giuliano Di Pietro	91
2	Abstract 2293: Oligomenorrhea, polycystic ovary syndrome, and risk of ovarian cancer histotypes, evidence from the Ovarian Cancer Association Consortium 2017 ·Cancer Research ·Holly R. Harris, Susan J. Jordan, Harvey A. Risch, Mary Anne Rossing, Marc T. Goodman, Francesmary Modugno, Susanne K. Kjær, Joellen M. Schildkraut, Elisa V. Bandera, Nicolas Wentzensen, Catherine Phelan, Hoda Anton‐Culver, Anna H. Wu, Kathryn L. Terry	1
3	Abstract 4635: Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility 2015 ·Cancer Research ·Jennifer Permuth‐Wey, Brett M. Reid, Y. Ann Chen, Hui‐Yi Lin, Álvaro N.A. Monteiro, Zhihua Chen, Andrew Berchuck, Georgia Chenevix‐Trench, Jennifer A. Doherty, Simon A. Gayther, Ellen L. Goode, Edwin S. Iversen, Leigh Pearce, Paul D.P. Pharoah, Catherine Phelan, Susan J. Ramus, (unknown), Joellen M. Schildkraut, Thomas A. Sellers	1
4	Differences in BRCA counseling and testing practices based on ordering provider type 2014 ·Genetics in Medicine ·Deborah Cragun, (unknown), Emily K. Robinson, (unknown), Jongphil Kim, Catherine Phelan, Álvaro N.A. Monteiro, Susan T. Vadaparampil, Thomas A. Sellers, Tuya Pal	42
5	BRCA1 and BRCA2 mutations and the risk for colorectal cancer 2014 ·Clinical Genetics ·Victoria Sopik, Catherine Phelan, Cezary Cybulski, Steven A. Narod	63
6	Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers 2013 ·Clinical Genetics ·Tuya Pal, Ji‐Hyun Lee, Aris Raad Besharat, Zachary Thompson, Álvaro N.A. Monteiro, Catherine Phelan, (unknown), Kelly Metcalfe, T. A. Sellers, Susan T. Vadaparampil, (unknown)	27
7	Impedance-Based Miniaturized Biosensor for Ultrasensitive and Fast Prostate-Specific Antigen Detection 2011 ·Journal of Sensors ·Ganna Chornokur, Sunil K. Arya, Catherine Phelan, (unknown), Shekhar Bhansali	27
8	Spectroscopic behavior of bioconjugated quantum dots 2008 ·Semiconductor Science and Technology ·Ganna Chornokur, S. Ostapenko, Yu. N. Émirov, N. Korsunska, Thomas A. Sellers, Catherine Phelan	9
9	Perfomance of WGA DNA in an Illumina GoldenGate BeadArray assay 2007 ·Julie M. Cunningham, Thomas A. Sellers, Joellen Schildkraut, Catherine Phelan, (unknown), Lynn C. Hartmann, Yifan Huang, Linda E. Kelemen, Janet E. Olson, Mark Liebow, Robert A. Vierkant, Zachary Fredericksen, Brian Calingaert, (unknown), (unknown), Ellen L. Goode	1
10	Raman scattering and SEM study of bio‐conjugated core‐shell CdSe/ZnS quantum dots 2007 ·Physica status solidi. C, Conferences and critical reviews/Physica status solidi. C, Current topics in solid state physics ·T.V. Torchynska, A. Cano, (unknown), S. Ostapenko, (unknown), S. Jiménez‐Sandoval, Yu. V. Vorobiev, Catherine Phelan, (unknown), Tatyana Zhukov, Thomas A. Sellers	21
11	Infliximab and serious hematologic events 2004 ·Canadian Medical Association Journal ·Catherine Phelan	7
12	Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2 2000 ·Nature Biotechnology ·Reyna Favis, Joseph Day, Norman P. Gerry, Catherine Phelan, Steven A. Narod, Francis Barany	172
13	An unaffected individual from a breast/ovarian cancer family with germline mutations in both BRCA1 and BRCA2 2000 ·Clinical Genetics ·Roxana Moslehi, Donna Russo, Catherine Phelan, Elaine Jack, Karen H. Antman, (unknown)	19
14	Identification of two distinct deleted regions on chromosome 13 in prostate cancer 1998 ·Oncogene ·Chunde Li, Catharina Larsson, P. Andrew Futreal, Jonathan Lancaster, Catherine Phelan, Ulla Aspenblad, Birgitta Sundelin, Yie Liu, Peter Ekman, Gert Auer, Ulf S.R. Bergerheim	74
15	Alterations of theMEN1Gene in Sporadic Parathyroid Tumors1 1998 ·The Journal of Clinical Endocrinology & Metabolism ·Filip Farnebo, Bin Tean Teh, Soili Kytölä, Ann Svensson, Catherine Phelan, Kerstin Sandelin, Norman W. Thompson, Anders Höög, Günther Weber, Lars‐Ove Farnebo, Catharina Larsson	132
16	Exclusion of the phosphoinositide-specific phospholipase C?3 ( PLCB3 ) gene as a candidate for multiple endocrine neoplasia type 1 1996 ·Human Genetics ·(unknown), Sean M. Grimmond, Jacob Lagercrantz, Eitan Friedman, Catherine Phelan, Emma Carson, Nicholas K. Hayward, (unknown), Magnus Nordenskj�ld, Catharina Larsson	6
17	Candidate genes for multiple endocrine neoplasia type 1 1995 ·Journal of Internal Medicine ·Jacob Lagercrantz, Catharina Larsson, Sean M. Grimmond, Britt Skogseid, A Gobl, Eitan Friedman, Emma Carson, Catherine Phelan, Kjell Öberg, Magnus Nordenskjöld, Nicholas K. Hayward, Griffin M. Weber	9
18	Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C β3 gene (PLCB3) 1995 ·Genomics ·Jacob Lagercrantz, Emma Carson, Catherine Phelan, Sean M. Grimmond, Anne Rosén, Elisabetta Daré, Magnus Nordenskjöld, Nicholas K. Hayward, Catharina Larsson, Günther Weber	16
19	Analysis of microsatellite repeats in pediatric brain tumors 1995 ·Cancer Genetics and Cytogenetics ·Ninette Amariglio, Eitan Friedman, Orna Mor, Hadas Stiebel‐Kalish, Catherine Phelan, (unknown), Magnus Nordenskjöld, F. Brok‐Simoni, Gidi Rechavi	15
20	The phospholipase C β3 gene located in the MEN1 region shows loss of expression in endocrine tumours 1994 ·Human Molecular Genetics ·Günther Weber, Eitan Friedman, Sean M. Grimmond, Nicholas K. Hayward, Catherine Phelan, Britt Skogseid, Anders Gobl, Jan Zedenius, Kerstin Sandelin, Bin Tean Teh, Emma Carson, I. White, Kjell Öberg, J. J. Shepherd, Magnus Nordenskjöld, Catharina Larsson	46

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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