Jennifer Holle

413 total citations
6 papers, 113 citations indexed

About

Jennifer Holle is a scholar working on Genetics, Infectious Diseases and Cancer Research. According to data from OpenAlex, Jennifer Holle has authored 6 papers receiving a total of 113 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Infectious Diseases and 2 papers in Cancer Research. Recurrent topics in Jennifer Holle's work include BRCA gene mutations in cancer (3 papers), Cancer Genomics and Diagnostics (2 papers) and Genomics and Rare Diseases (2 papers). Jennifer Holle is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Cancer Genomics and Diagnostics (2 papers) and Genomics and Rare Diseases (2 papers). Jennifer Holle collaborates with scholars based in United States, Australia and India. Jennifer Holle's co-authors include Scott T. Michalski, Karen Ouyang, Erin O’Leary, Shan Yang, Edward D. Esplin, Xun Zhang, Kathleen Collins, Melanie F. Myers, C. Alexander Valencia and Kejian Zhang and has published in prestigious journals such as Journal of Clinical Oncology, Annals of Surgical Oncology and Pediatric Blood & Cancer.

In The Last Decade

Jennifer Holle

6 papers receiving 112 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer Holle United States	5	75	31	30	22	18	6	113
Shiho Nishimura Japan	7	31 0.4×	51 1.6×	52 1.7×	4 0.2×	9 0.5×	19	135
Anna Wakulińska Poland	7	29 0.4×	91 2.9×	58 1.9×	16 0.7×	32 1.8×	10	163
Björn Stade Germany	4	88 1.2×	34 1.1×	75 2.5×	8 0.4×	22 1.2×	5	158
Sushree Sangita Sahoo United States	6	40 0.5×	35 1.1×	37 1.2×	8 0.4×	10 0.6×	13	136
Sonoko Sakata Japan	7	36 0.5×	32 1.0×	44 1.5×	7 0.3×	8 0.4×	8	99
Анастасія Бондаренко Ukraine	5	51 0.7×	14 0.5×	109 3.6×	10 0.5×	9 0.5×	17	143
Sandra Fert‐Ferrer France	7	39 0.5×	46 1.5×	8 0.3×	17 0.8×	12 0.7×	10	117
Tzu‐Wen Yeh Japan	5	35 0.5×	16 0.5×	82 2.7×	5 0.2×	8 0.4×	5	108
Svetlana Vakkilainen Finland	7	32 0.4×	53 1.7×	70 2.3×	12 0.5×	18 1.0×	18	133
Marie V. Coignet United States	6	17 0.2×	21 0.7×	33 1.1×	17 0.8×	5 0.3×	8	123

Countries citing papers authored by Jennifer Holle

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Holle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Holle

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

All Works

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6 of 6 papers shown

1.

Quinn, Jessica, Vicki Modell, Jennifer Holle, et al.. (2020). Jeffrey’s insights: Jeffrey Modell Foundation’s global genetic sequencing pilot program to identify specific primary immunodeficiency defects to optimize disease management and treatment. Immunologic Research. 68(3). 126–134. 18 indexed citations

2.

Yohe, Sophia, Sivasankar Malaichamy, Anuprita Ghosh, et al.. (2019). Prevalence of mutations in inherited retinal diseases: A comparison between the United States and India. Molecular Genetics & Genomic Medicine. 8(2). e1081–e1081. 14 indexed citations

3.

O’Leary, Erin, Jennifer Holle, Scott T. Michalski, et al.. (2017). Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk. Annals of Surgical Oncology. 24(10). 3060–3066. 47 indexed citations

4.

Yang, Shan, Scott T. Michalski, Jennifer Holle, et al.. (2017). Unexpected germline mutations in a pan-cancer analysis including sarcoma, renal, and other cancers.. Journal of Clinical Oncology. 35(15_suppl). 1584–1584. 1 indexed citations

5.

Collins, Kathleen, et al.. (2016). Pediatric Whole Exome Sequencing: an Assessment of Parents’ Perceived and Actual Understanding.. Journal of Genetic Counseling. 26(4). 792–805. 17 indexed citations

6.

Holle, Jennifer, Rebecca Marsh, Stella M. Davies, et al.. (2015). Hemophagocytic lymphohistiocytosis in a female patient due to a heterozygous XIAP mutation and skewed X chromosome inactivation. Pediatric Blood & Cancer. 62(7). 1288–1290. 16 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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