John J. Connolly

6.4k total citations
72 papers, 1.8k citations indexed

About

John J. Connolly is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, John J. Connolly has authored 72 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 11 papers in Molecular Biology and 11 papers in Public Health, Environmental and Occupational Health. Recurrent topics in John J. Connolly's work include Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (8 papers) and Ethics in Clinical Research (8 papers). John J. Connolly is often cited by papers focused on Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (8 papers) and Ethics in Clinical Research (8 papers). John J. Connolly collaborates with scholars based in United States, Iceland and China. John J. Connolly's co-authors include Håkon Håkonarson, Frank Mentch, Rosetta Chiavacci, Monica E. Calkins, Haijun Qiu, Raquel E. Gur, Ruben C. Gur, Joseph Glessner, Warren B. Bilker and John F. Moorhead and has published in prestigious journals such as The Journal of Chemical Physics, SHILAP Revista de lepidopterología and The Journal of Immunology.

In The Last Decade

John J. Connolly

63 papers receiving 1.7k citations

Peers

John J. Connolly
Frank Mentch United States
Haijun Qiu United States
Shin‐Ichi Niwa Japan
Michael Johnson United States
Smita N. Deshpande India
Yi Lu Sweden
Patricia Kozuch United States
Esther Gómez‐Gil Spain
Yushiro Yamashita Japan
Katharine Smith United Kingdom
Frank Mentch United States
John J. Connolly
Citations per year, relative to John J. Connolly John J. Connolly (= 1×) peers Frank Mentch

Countries citing papers authored by John J. Connolly

Since Specialization
Citations

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

Fields of papers citing papers by John J. Connolly

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John J. Connolly. 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 John J. Connolly. The network helps show where John J. Connolly may publish in the future.

Co-authorship network of co-authors of John J. Connolly

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

All Works

20 of 20 papers shown
1.
2.
3.
Qu, Hui‐Qi, Joseph Glessner, Yichuan Liu, et al.. (2023). High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations. Translational research. 266. 49–56.
4.
Qu, Hui‐Qi, John J. Connolly, Peter Kraft, et al.. (2023). Trans‐ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium study. Clinical and Translational Medicine. 13(6). e1291–e1291. 3 indexed citations
5.
Bakken, Suzanne, John Lynch, Wendy K. Chung, et al.. (2023). Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study. Journal of the American Medical Informatics Association. 31(2). 306–316. 2 indexed citations
6.
Glessner, Joseph, Xiao Chang, Yichuan Liu, et al.. (2023). Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 15(1). 14–14. 5 indexed citations
7.
Clayton, Ellen Wright, Maureen E. Smith, Wendy K. Chung, et al.. (2023). Studying the impact of translational genomic research: Lessons from eMERGE. The American Journal of Human Genetics. 110(7). 1021–1033. 7 indexed citations
8.
Lee, Jung‐Eun, John J. Connolly, Wen Yang, et al.. (2022). Fibrous anisotropy and mineral gradients within the radula stylus of chiton: Controlled stiffness and damage tolerance in a flexible biological composite. Journal of Composite Materials. 57(4). 565–574. 2 indexed citations
9.
Feng, Yen‐Chen Anne, Ian B. Stanaway, John J. Connolly, et al.. (2022). Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach. BMC Genomics. 23(1). 385–385. 4 indexed citations
10.
Qu, Hui‐Qi, Joseph Glessner, Frank Mentch, et al.. (2022). Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans. iScience. 25(7). 104650–104650. 8 indexed citations
11.
Qu, Hui‐Qi, Joseph Glessner, Frank Mentch, et al.. (2022). Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium. Metabolomics. 18(12). 101–101. 4 indexed citations
12.
Hoell, Christin, Julia Wynn, Luke V. Rasmussen, et al.. (2020). Participant choices for return of genomic results in the eMERGE Network. Genetics in Medicine. 22(11). 1821–1829. 24 indexed citations
13.
Almoguera, Berta, Lyam Vazquez, Frank Mentch, et al.. (2018). Novel locus for atopic dermatitis in African Americans and replication in European Americans. Journal of Allergy and Clinical Immunology. 143(3). 1229–1231. 8 indexed citations
14.
Overby, Casey Lynnette, John J. Connolly, Christopher G. Chute, et al.. (2016). Practical considerations for implementing genomic information resources. Applied Clinical Informatics. 7(3). 870–882. 22 indexed citations
15.
Kullo, Iftikhar J., Raad A. Haddad, Cynthia A. Prows, et al.. (2014). Return of results in the genomic medicine projects of the eMERGE network. Frontiers in Genetics. 5. 50–50. 36 indexed citations
16.
Almoguera, Berta, Lyam Vazquez, John J. Connolly, et al.. (2014). Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes. Frontiers in Genetics. 5. 96–96. 12 indexed citations
17.
Sleiman, Patrick, Jonathan P. Bradfield, Frank Mentch, et al.. (2014). Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts. Frontiers in Genetics. 5. 105–105. 3 indexed citations
18.
Kho, Abel, Luke V. Rasmussen, John J. Connolly, et al.. (2013). Practical challenges in integrating genomic data into the electronic health record. Genetics in Medicine. 15(10). 772–778. 69 indexed citations
19.
Gur, Ruben C., Jan Richard, Monica E. Calkins, et al.. (2012). Age group and sex differences in performance on a computerized neurocognitive battery in children age 8−21.. Neuropsychology. 26(2). 251–265. 377 indexed citations
20.
Connolly, John J.. (1990). "Reasonable Particularity" in Indictments Against Child Abusers. Maryland law review. 49(4). 1008. 2 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

Breakdown of academic impact, for papers by Frank Mentch Breakdown of academic impact, for papers by Haijun Qiu Breakdown of academic impact, for papers by Shin‐Ichi Niwa Breakdown of academic impact, for papers by Michael Johnson Breakdown of academic impact, for papers by Smita N. Deshpande Breakdown of academic impact, for papers by Yi Lu Breakdown of academic impact, for papers by Patricia Kozuch Breakdown of academic impact, for papers by Esther Gómez‐Gil Breakdown of academic impact, for papers by Yushiro Yamashita Breakdown of academic impact, for papers by Katharine Smith
Rankless by CCL
2026