Patrick Concannon

29.4k total citations · 4 hit papers
228 papers, 15.8k citations indexed

About

Patrick Concannon is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Patrick Concannon has authored 228 papers receiving a total of 15.8k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Genetics, 100 papers in Molecular Biology and 66 papers in Immunology. Recurrent topics in Patrick Concannon's work include DNA Repair Mechanisms (64 papers), Diabetes and associated disorders (58 papers) and T-cell and B-cell Immunology (53 papers). Patrick Concannon is often cited by papers focused on DNA Repair Mechanisms (64 papers), Diabetes and associated disorders (58 papers) and T-cell and B-cell Immunology (53 papers). Patrick Concannon collaborates with scholars based in United States, United Kingdom and Denmark. Patrick Concannon's co-authors include Richard A. Gatti, Stephen S. Rich, Karen Cerosaletti, John A. Todd, Suna Önengüt-Gümüşcü, Eric Lai, Leroy Hood, L Hood, Cécile Julier and Flemming Pociot and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Patrick Concannon

227 papers receiving 15.4k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

2009 1.3k citations Patrick Concannon, John A. Todd et al. profile →
Gut Microbiomes of Malawian Twin Pairs Discordant for Kwashiorkor

2013 826 citations Michelle I. Smith, Tanya Yatsunenko et al. Science profile →
Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

1998 811 citations Raymonda Varon, Christine Vissinga et al. Cell profile →
HLA DR-DQ Haplotypes and Genotypes and Type 1 Diabetes Risk

2008 570 citations Patrick Concannon, Josyf C. Mychaleckyj et al. Diabetes profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Patrick Concannon	7.6k	6.0k	3.9k	2.7k	2.7k	228	15.8k
Steven P. Balk	7.2k 1.0×	3.2k 0.5×	7.7k 2.0×	737 0.3×	3.6k 1.4×	241	20.9k
Audrey D. Goddard	9.8k 1.3×	2.1k 0.4×	3.9k 1.0×	894 0.3×	3.2k 1.2×	70	15.8k
Flemming Pociot	4.6k 0.6×	7.2k 1.2×	4.5k 1.1×	5.2k 2.0×	839 0.3×	326	16.2k
Takehiko Sasazuki	5.8k 0.8×	2.5k 0.4×	8.2k 2.1×	1.1k 0.4×	2.9k 1.1×	351	18.7k
Lorenzo Piemonti	3.4k 0.5×	3.1k 0.5×	3.9k 1.0×	4.7k 1.8×	2.7k 1.0×	290	13.5k
Christopher G. Mathew	7.3k 1.0×	6.4k 1.1×	2.3k 0.6×	2.1k 0.8×	1.6k 0.6×	246	14.2k
Agnès Viale	12.1k 1.6×	1.8k 0.3×	2.0k 0.5×	1.4k 0.5×	5.4k 2.0×	139	20.7k
Giuseppe Novelli	8.1k 1.1×	2.2k 0.4×	2.1k 0.5×	1.5k 0.6×	765 0.3×	636	15.5k
Evan T. Keller	8.4k 1.1×	1.6k 0.3×	2.6k 0.7×	1.2k 0.5×	7.5k 2.8×	275	18.2k
Peter K. Gregersen	4.6k 0.6×	4.8k 0.8×	10.5k 2.7×	825 0.3×	2.4k 0.9×	283	22.5k

Countries citing papers authored by Patrick Concannon

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Concannon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Concannon

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

Reiner, Anne S., Gordon P. Watt, Kathleen E. Malone, et al.. (2024). Breast Cancer Susceptibility Gene Sequence Variations and Development of Contralateral Breast Cancer. JAMA Network Open. 7(12). e2452158–e2452158. 1 indexed citations

Dong, Xiaoru, Daniel J. Perry, Amanda L. Posgai, et al.. (2023). Human immune phenotyping reveals accelerated aging in type 1 diabetes. JCI Insight. 8(17). 21 indexed citations

Larionov, Alexey A., Eleanor Fewings, James Redman, et al.. (2023). The Contribution of Germline Pathogenic Variants in Breast Cancer Genes to Contralateral Breast Cancer Risk in BRCA1/BRCA2/PALB2-Negative Women. Cancers. 15(2). 415–415. 1 indexed citations

Newman, Jeremy R. B., S. Alice Long, Cate Speake, et al.. (2023). Shifts in isoform usage underlie transcriptional differences in regulatory T cells in type 1 diabetes. Communications Biology. 6(1). 988–988. 2 indexed citations

Balzano‐Nogueira, Leandro, Alexandria N. Ardissone, Srikar Chamala, et al.. (2021). Integrative analyses of TEDDY Omics data reveal lipid metabolism abnormalities, increased intracellular ROS and heightened inflammation prior to autoimmunity for type 1 diabetes. Genome biology. 22(1). 39–39. 22 indexed citations

Newman, Jeremy R. B., et al.. (2021). Genetic Control of Splicing at SIRPG Modulates Risk of Type 1 Diabetes. Diabetes. 71(2). 350–358. 2 indexed citations

Wojcik, Genevieve L., Poonum Korpe, Chelsea Marie, et al.. (2020). Genome-Wide Association Study of Cryptosporidiosis in Infants Implicates PRKCA. mBio. 11(1). 16 indexed citations

Smith, Michelle I., Tanya Yatsunenko, Mark Manary, et al.. (2013). Gut Microbiomes of Malawian Twin Pairs Discordant for Kwashiorkor. Science. 339(6119). 548–554. 826 indexed citations breakdown →

Jia, Xiaoming, Buhm Han, Suna Önengüt-Gümüşcü, et al.. (2013). Imputing Amino Acid Polymorphisms in Human Leukocyte Antigens. PLoS ONE. 8(6). e64683–e64683. 352 indexed citations

10.

Demuth, Ilja, Paul S. Bradshaw, Julia Kallenbach, et al.. (2008). Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation. DNA repair. 7(8). 1192–1201. 28 indexed citations

11.

Rieck, Mary, Adrian F. Arechiga, Suna Önengüt-Gümüşcü, et al.. (2007). Genetic Variation in PTPN22 Corresponds to Altered Function of T and B Lymphocytes. The Journal of Immunology. 179(7). 4704–4710. 266 indexed citations

12.

Demuth, Ilja, Martin Digweed, & Patrick Concannon. (2004). Human SNM1B is required for normal cellular response to both DNA interstrand crosslink-inducing agents and ionizing radiation. Oncogene. 23(53). 8611–8618. 62 indexed citations

13.

O’Driscoll, Mark, Andrew R. Gennery, J. Seidel, Patrick Concannon, & Penelope A. Jeggo. (2004). An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome. DNA repair. 3(8-9). 1227–1235. 145 indexed citations

14.

Concannon, Patrick, et al.. (2002). Complementarity-Determining Region 1 Sequence Requirements Drive Limited Vα Usage in Response to Influenza Hemagglutinin 307–319 Peptide. The Journal of Immunology. 168(8). 3894–3901. 3 indexed citations

15.

Desai‐Mehta, Ami, Karen Cerosaletti, & Patrick Concannon. (2001). Distinct Functional Domains of Nibrin Mediate Mre11 Binding, Focus Formation, and Nuclear Localization. Molecular and Cellular Biology. 21(6). 2184–2191. 159 indexed citations

16.

Cox, Nancy J., Beth Wapelhorst, Victoria Morrison, et al.. (2001). Seven Regions of the Genome Show Evidence of Linkage to Type 1 Diabetes in a Consensus Analysis of 767 Multiplex Families. The American Journal of Human Genetics. 69(4). 820–830. 203 indexed citations

17.

Teraoka, Sharon N., Milhan Telatar, Sara Becker-Catania, et al.. (1999). Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences. The American Journal of Human Genetics. 64(6). 1617–1631. 239 indexed citations

18.

Varon, Raymonda, Christine Vissinga, Matthias Platzer, et al.. (1998). Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome. Cell. 93(3). 467–476. 811 indexed citations breakdown →

19.

Posnett, David N., Christine Vissinga, Wei Shan, et al.. (1994). Level of human TCRBV3S1 (V beta 3) expression correlates with allelic polymorphism in the spacer region of the recombination signal sequence.. The Journal of Experimental Medicine. 179(5). 1707–1711. 69 indexed citations

20.

Concannon, Patrick, Richard A. Gatti, & Leroy Hood. (1987). Human T cell receptor V beta gene polymorphism.. The Journal of Experimental Medicine. 165(4). 1130–1140. 89 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.

Explore authors with similar magnitude of impact