Jennifer Ivanovich

6.1k total citations · 1 hit paper
34 papers, 1.8k citations indexed

About

Jennifer Ivanovich is a scholar working on Genetics, Cancer Research and Oncology. According to data from OpenAlex, Jennifer Ivanovich has authored 34 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Cancer Research and 10 papers in Oncology. Recurrent topics in Jennifer Ivanovich's work include BRCA gene mutations in cancer (11 papers), Cancer Genomics and Diagnostics (9 papers) and Genetic factors in colorectal cancer (8 papers). Jennifer Ivanovich is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Cancer Genomics and Diagnostics (9 papers) and Genetic factors in colorectal cancer (8 papers). Jennifer Ivanovich collaborates with scholars based in United States, France and Germany. Jennifer Ivanovich's co-authors include Paul J. Goodfellow, Alison J. Whelan, Louis P. Dehner, Yoav H. Messinger, D. Ashley Hill, Kathryn A. Wikenheiser‐Brokamp, Christina A. Gurnett, Gretchen M. Williams, Brian K. Suarez and John R. Priest and has published in prestigious journals such as Science, Blood and The Journal of Immunology.

In The Last Decade

Jennifer Ivanovich

33 papers receiving 1.8k 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.

DICER1 Mutations in Familial Pleuropulmonary Blastoma

2009 484 citations D. Ashley Hill, Jennifer Ivanovich et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer Ivanovich United States	17	622	419	377	348	311	34	1.8k
Eevi Kaasinen Finland	24	1.6k 2.6×	743 1.8×	303 0.8×	318 0.9×	314 1.0×	49	3.4k
C. Sue Richards United States	20	934 1.5×	180 0.4×	913 2.4×	386 1.1×	434 1.4×	41	2.3k
Sabine Bartnitzke Germany	30	680 1.1×	483 1.2×	540 1.4×	317 0.9×	524 1.7×	109	2.4k
Tauro Maria Neri Italy	21	591 1.0×	179 0.4×	332 0.9×	123 0.4×	609 2.0×	51	2.2k
Junne Kamihara United States	14	608 1.0×	341 0.8×	238 0.6×	310 0.9×	296 1.0×	40	1.5k
Ingrid Laurendeau France	22	467 0.8×	403 1.0×	112 0.3×	405 1.2×	122 0.4×	35	1.7k
Denis Bailey Canada	25	566 0.9×	665 1.6×	196 0.5×	178 0.5×	924 3.0×	59	2.1k
C.A. Griffin United States	21	795 1.3×	180 0.4×	267 0.7×	185 0.5×	419 1.3×	41	2.1k
Wolfram Henn Germany	23	1.5k 2.4×	292 0.7×	425 1.1×	405 1.2×	590 1.9×	78	2.7k
Filip Farnebo Sweden	34	1.4k 2.2×	485 1.2×	632 1.7×	377 1.1×	1.0k 3.3×	71	3.4k

Countries citing papers authored by Jennifer Ivanovich

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Ivanovich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Ivanovich

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

Wetherill, Leah, et al.. (2024). Exploring Genetic Counselors’ Experiences with Indigenous Patient Populations. Journal of Racial and Ethnic Health Disparities. 12(6). 3979–3990. 1 indexed citations

Wetherill, Leah, et al.. (2024). Exploring genetic counselors' interest and role in transitional care discussions for pediatric patients with neurodevelopmental conditions. Journal of Genetic Counseling. 34(3). e1992–e1992. 1 indexed citations

Marshall, Mark S., et al.. (2023). Pediatric precision oncology: “better three hours too soon than a minute too late”. Frontiers in Oncology. 13. 1279953–1279953.

Wetherill, Leah, et al.. (2022). Diversity training experiences and factors associated with implicit racial bias among recent genetic counselor graduates of accredited programs in the United States and Canada. Journal of Genetic Counseling. 31(3). 792–802. 8 indexed citations

Marshall, Mark S., et al.. (2020). Sustained Complete Response to Palbociclib in a Refractory Pediatric Sarcoma With BCOR-CCNB3 Fusion and Germline CDKN2B Variant. PMC. 3 indexed citations

Ivanovich, Jennifer, Marc R. Radke, Marcy E. Richardson, et al.. (2019). Rare BRIP1 Missense Alleles Confer Risk for Ovarian and Breast Cancer. Cancer Research. 80(4). 857–867. 33 indexed citations

Hong, Soo Jung, Barbara B. Biesecker, Jennifer Ivanovich, Melody S. Goodman, & Kimberly A. Kaphingst. (2019). Factors affecting breast cancer patients' need for genetic risk information: From information insufficiency to information need. Journal of Genetic Counseling. 28(3). 543–557. 9 indexed citations

Walker, Christopher J., James S. Blachly, Jennifer Ivanovich, et al.. (2016). MonoSeq Variant Caller Reveals Novel Mononucleotide Run Indel Mutations in Tumors with Defective DNA Mismatch Repair. Human Mutation. 37(10). 1004–1012. 5 indexed citations

Ademuyiwa, Foluso O., Amy Cyr, Jennifer Ivanovich, & Maria Thomas. (2015). Managing breast cancer in younger women: challenges and solutions. Breast Cancer Targets and Therapy. 8. 1–1. 31 indexed citations

10.

Hill, D. Ashley, Jennifer Ivanovich, John R. Priest, et al.. (2009). DICER1 Mutations in Familial Pleuropulmonary Blastoma. Science. 325(5943). 965–965. 484 indexed citations breakdown →

11.

Du, Hongyan, Rachel A. Idol, Sara M. Robledo, et al.. (2007). Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p– syndrome. Aging Cell. 6(5). 689–697. 24 indexed citations

12.

Pham, Christine T. N., Jennifer Ivanovich, Sofia Z. Raptis, Barbara A. Zehnbauer, & Timothy J. Ley. (2004). Papillon-Lefevre Syndrome: Correlating the Molecular, Cellular, and Clinical Consequences of Cathepsin C/Dipeptidyl Peptidase I Deficiency in Humans. The Journal of Immunology. 173(12). 7277–7281. 162 indexed citations

13.

Zhou, Xiao-Ping, Kristin Waite, Robert Pilarski, et al.. (2003). Germline PTEN Promoter Mutations and Deletions in Cowden/Bannayan-Riley-Ruvalcaba Syndrome Result in Aberrant PTEN Protein and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pathway. The American Journal of Human Genetics. 73(2). 404–411. 199 indexed citations

14.

Whelan, Alison J., David G. Mutch, Janet S. Rader, et al.. (2002). MSI in endometrial carcinoma: Absence of MLH1 promoter methylation is associated with increased familial risk for cancers. International Journal of Cancer. 99(5). 697–704. 35 indexed citations

15.

Ivanovich, Jennifer, et al.. (2001). 12-year-old male with Elejalde syndrome (neuroectodermal melanolysosomal disease). American Journal of Medical Genetics. 98(4). 313–316. 15 indexed citations

16.

Skinner, Celette Sugg, et al.. (2001). Perceptions of genetic risk assessment and education among first-degree relatives of colorectal cancer patients and implications for physicians. Family Practice. 18(4). 367–372. 5 indexed citations

17.

Ivanovich, Jennifer, Michael S. Watson, & Alison J. Whelan. (2001). An 11-year-old boy with mosaic ring chromosome 6 and dilated aortic root. American Journal of Medical Genetics. 98(2). 182–184. 7 indexed citations

18.

Ivanovich, Jennifer, et al.. (1999). A practical approach to familial and hereditary colorectal cancer. The American Journal of Medicine. 107(1). 68–77. 31 indexed citations

19.

Whelan, Alison J., et al.. (1997). Mutations inMLH1 are more frequent than inMSH2 in sporadic colorectal cancers with microsatellite instability. Genes Chromosomes and Cancer. 18(1). 42–49. 50 indexed citations

20.

Wells, Samuel A., Doina David, Koji Toshima, et al.. (1994). Predictive DNA Testing and Prophylactic Thyroidectomy in Patients at Risk for Multiple Endocrine Neoplasia Type 2A. Annals of Surgery. 220(3). 237–250. 303 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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