Peter J. Hulick

7.1k total citations
46 papers, 852 citations indexed

About

Peter J. Hulick is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Peter J. Hulick has authored 46 papers receiving a total of 852 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 10 papers in Pulmonary and Respiratory Medicine and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Peter J. Hulick's work include BRCA gene mutations in cancer (17 papers), Genetic Associations and Epidemiology (10 papers) and Pharmacogenetics and Drug Metabolism (7 papers). Peter J. Hulick is often cited by papers focused on BRCA gene mutations in cancer (17 papers), Genetic Associations and Epidemiology (10 papers) and Pharmacogenetics and Drug Metabolism (7 papers). Peter J. Hulick collaborates with scholars based in United States, Australia and Singapore. Peter J. Hulick's co-authors include Henry M. Dunnenberger, Christina G. Selkirk, Scott M. Weissman, Andy Anderson, Amy A. Lemke, Dyson T. Wake, Katharine Yao, David J. Winchester, Nicole Glaser and Michael A. Howard and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Peter J. Hulick

44 papers receiving 828 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Peter J. Hulick United States	16	375	227	181	143	139	46	852
Christopher Sanders United States	11	201 0.5×	228 1.0×	151 0.8×	123 0.9×	81 0.6×	18	833
Katherine Johansen Taber United States	14	481 1.3×	314 1.4×	328 1.8×	102 0.7×	26 0.2×	31	1.1k
Julie A. Cakici United States	9	505 1.3×	76 0.3×	108 0.6×	79 0.6×	35 0.3×	12	722
Tessel Rigter Netherlands	14	276 0.7×	57 0.3×	184 1.0×	24 0.2×	68 0.5×	34	646
Katherine Kolor United States	16	508 1.4×	43 0.2×	91 0.5×	132 0.9×	98 0.7×	28	957
Alka Malhotra United States	14	185 0.5×	114 0.5×	62 0.3×	44 0.3×	253 1.8×	30	1.1k
Teresa Kruisselbrink United States	11	214 0.6×	52 0.2×	35 0.2×	47 0.3×	71 0.5×	23	744
Monica Fujii United States	10	99 0.3×	37 0.2×	42 0.2×	106 0.7×	59 0.4×	28	561
Christina Mitropoulou Greece	15	208 0.6×	237 1.0×	86 0.5×	57 0.4×	14 0.1×	42	562
Johanie Lépine Canada	13	258 0.7×	271 1.2×	179 1.0×	56 0.4×	27 0.2×	21	843

Countries citing papers authored by Peter J. Hulick

Since Specialization

Citations

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

Fields of papers citing papers by Peter J. Hulick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter J. Hulick

This figure shows the co-authorship network connecting the top 25 collaborators of Peter J. Hulick. A scholar is included among the top collaborators of Peter J. Hulick 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 Peter J. Hulick. Peter J. Hulick 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

Billings, Liana K., Zhuqing Shi, Jun Wei, et al.. (2023). Utility of Polygenic Scores for Differentiating Diabetes Diagnosis Among Patients With Atypical Phenotypes of Diabetes. The Journal of Clinical Endocrinology & Metabolism. 109(1). 107–113. 4 indexed citations

Xu, Jianfeng, Zhuqing Shi, Jun Wei, et al.. (2022). Inherited risk assessment and its clinical utility for predicting prostate cancer from diagnostic prostate biopsies. Prostate Cancer and Prostatic Diseases. 25(3). 422–430. 14 indexed citations

Shi, Zhuqing, Jun Wei, Brian T. Helfand, et al.. (2022). Reclassification of coronary artery disease risk using genetic risk score among subjects with borderline or intermediate clinical risk. IJC Heart & Vasculature. 43. 101136–101136. 3 indexed citations

Shi, Zhuqing, Jianan Zhan, Jun Wei, et al.. (2022). Reliability of Ancestry-specific Prostate Cancer Genetic Risk Score in Four Racial and Ethnic Populations. European Urology Open Science. 45. 23–30. 6 indexed citations

Wei, Jun, Wancai Yang, Zhuqing Shi, et al.. (2021). Observed evidence for guideline‐recommended genes in predicting prostate cancer risk from a large population‐based cohort. The Prostate. 81(13). 1002–1008. 10 indexed citations

Lemke, Amy A., Laura M. Amendola, Jennifer Thompson, et al.. (2021). Patient-Reported Outcomes and Experiences with Population Genetic Testing Offered Through a Primary Care Network. Genetic Testing and Molecular Biomarkers. 25(2). 152–160. 20 indexed citations

David, Sean P., et al.. (2021). Implementing Primary Care Mediated Population Genetic Screening Within an Integrated Health System. The Journal of the American Board of Family Medicine. 34(4). 861–865. 20 indexed citations

Lemke, Amy A., Laura M. Amendola, Kristine Kuchta, et al.. (2020). Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment. Journal of Personalized Medicine. 10(4). 165–165. 26 indexed citations

Lemke, Amy A., Jennifer Thompson, Peter J. Hulick, et al.. (2020). Primary care physician experiences utilizing a family health history tool with electronic health record–integrated clinical decision support: an implementation process assessment. Journal of Community Genetics. 11(3). 339–350. 16 indexed citations

10.

Wei, Jun, Zhuqing Shi, Rong Na, et al.. (2020). Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank. British Journal of Cancer. 123(9). 1356–1359. 13 indexed citations

11.

Shi, Zhuqing, Elizabeth A. Platz, Jun Wei, et al.. (2020). Performance of Three Inherited Risk Measures for Predicting Prostate Cancer Incidence and Mortality: A Population-based Prospective Analysis. European Urology. 79(3). 419–426. 36 indexed citations

12.

Hedeker, Donald, Sarah M. Nielsen, Mary B. Daly, et al.. (2019). Hematologic toxicity in BRCA1 and BRCA2 mutation carriers during chemotherapy: A retrospective matched cohort study. Cancer Medicine. 8(12). 5609–5618. 7 indexed citations

13.

Wake, Dyson T., et al.. (2019). Pharmacogenomics. Medical Clinics of North America. 103(6). 977–990. 35 indexed citations

14.

Selkirk, Christina G., Kristen J. Vogel, Anna Newlin, et al.. (2014). Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice. Familial Cancer. 13(4). 527–536. 29 indexed citations

15.

Yao, Katharine, Erik Liederbach, Rong Tang, et al.. (2014). Nipple-Sparing Mastectomy in BRCA1/2 Mutation Carriers: An Interim Analysis and Review of the Literature. Annals of Surgical Oncology. 22(2). 370–376. 88 indexed citations

16.

Selkirk, Christina G., Scott M. Weissman, Andy Anderson, & Peter J. Hulick. (2013). Physicians' Preparedness for Integration of Genomic and Pharmacogenetic Testing into Practice Within a Major Healthcare System. Genetic Testing and Molecular Biomarkers. 17(3). 219–225. 104 indexed citations

17.

Neil, Christopher R., Peter J. Hulick, Tomáš Rejtar, et al.. (2013). Human Folliculin Delays Cell Cycle Progression through Late S and G2/M-Phases: Effect of Phosphorylation and Tumor Associated Mutations. PLoS ONE. 8(7). e66775–e66775. 15 indexed citations

18.

Hulick, Peter J.. (2011). Personal Genome Analysis. Internal Medicine News. 44(18). 36–37. 1 indexed citations

19.

Hulick, Peter J., Kristin Noonan, Diana Donovan, et al.. (2009). Cytogenetic and Array-CGH Characterization of a Complex de novo Rearrangement Involving Duplication and Deletion of 9p and Clinical Findings in a 4-Month-Old Female. Cytogenetic and Genome Research. 126(3). 305–312. 20 indexed citations

20.

Martin, Eric S., et al.. (2000). Bernard-Soulier syndrome: Common ancestry in two African American families with the GP Ib? Leu129Pro mutation. American Journal of Hematology. 65(2). 141–148. 9 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.

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