Jillene Kogan

569 total citations
13 papers, 217 citations indexed

About

Jillene Kogan is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jillene Kogan has authored 13 papers receiving a total of 217 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jillene Kogan's work include Renal and related cancers (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Renal cell carcinoma treatment (3 papers). Jillene Kogan is often cited by papers focused on Renal and related cancers (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Renal cell carcinoma treatment (3 papers). Jillene Kogan collaborates with scholars based in United States, Germany and Bosnia and Herzegovina. Jillene Kogan's co-authors include René G. VanDeVoorde, Elizabeth K. Schorry, David P. Witte, Jens Goebel, Jeffrey A. Whitsett, Kathy E. Wedig, John C. Egelhoff, Howard M. Saal, Robert J. Hopkin and A. James Barkovich and has published in prestigious journals such as PEDIATRICS, Clinical Genetics and Journal of Perinatology.

In The Last Decade

Jillene Kogan

12 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jillene Kogan United States 9 105 94 55 34 29 13 217
Kimiaki Uetake Japan 7 61 0.6× 88 0.9× 25 0.5× 40 1.2× 24 0.8× 16 175
Frédérique Tihy Canada 11 120 1.1× 215 2.3× 41 0.7× 146 4.3× 23 0.8× 18 384
K Lillquist Denmark 8 381 3.6× 212 2.3× 35 0.6× 36 1.1× 33 1.1× 14 523
Gabriela Stangoni Italy 9 122 1.2× 166 1.8× 14 0.3× 35 1.0× 7 0.2× 24 257
B.N. Chodirker Canada 10 113 1.1× 130 1.4× 7 0.1× 71 2.1× 36 1.2× 17 355
Sandesh C. Sreenath Nagamani United States 6 194 1.8× 218 2.3× 7 0.1× 70 2.1× 12 0.4× 8 349
Melanie Chan United Kingdom 9 96 0.9× 72 0.8× 57 1.0× 12 0.4× 10 0.3× 17 290
Julie Kaylor United States 9 103 1.0× 104 1.1× 21 0.4× 35 1.0× 11 0.4× 11 206
Lily Hoffman‐Andrews United States 5 99 0.9× 119 1.3× 4 0.1× 24 0.7× 21 0.7× 11 240
Caroline Bénech France 8 132 1.3× 196 2.1× 13 0.2× 41 1.2× 16 0.6× 14 278

Countries citing papers authored by Jillene Kogan

Since Specialization
Citations

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

Fields of papers citing papers by Jillene Kogan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jillene Kogan

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

All Works

13 of 13 papers shown
1.
Roth, Christian, et al.. (2021). Congenital cervical spine malformation due to bi‐allelic RIPPLY2 variants in spondylocostal dysostosis type 6. Clinical Genetics. 99(4). 565–571. 3 indexed citations
2.
Kurtović-Kozarić, Amina, Faruk Skenderi, Ondřej Hes, et al.. (2020). KANK1-NTRK3 fusions define a subset of BRAF mutation negative renal metanephric adenomas. BMC Medical Genetics. 21(1). 202–202. 6 indexed citations
3.
4.
Kurtović-Kozarić, Amina, Faruk Skenderi, Ondřej Hes, et al.. (2018). 23. Prevalence of KANK1-NTRK3 fusion in renal metanephric adenomas that lack BRAF mutations. Cancer Genetics. 224-225. 59–59. 1 indexed citations
5.
6.
Ticho, Benjamin H., et al.. (2015). A familial pericentric inversion of chromosome 11 associated with a microdeletion of 163kb and microduplication of 288kb at 11p13 and 11q22.3 without aniridia or eye anomalies. American Journal of Medical Genetics Part A. 170(1). 202–209. 8 indexed citations
7.
Aldinger, Kimberly A., Jillene Kogan, Virginia Kimonis, et al.. (2012). Cerebellar and posterior fossa malformations in patients with autism‐associated chromosome 22q13 terminal deletion. American Journal of Medical Genetics Part A. 161(1). 131–136. 51 indexed citations
8.
Kogan, Jillene, Erin Miller, & Stephanie M. Ware. (2009). High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: Delineating novel loci for apraxia. American Journal of Medical Genetics Part A. 149A(5). 887–893. 9 indexed citations
9.
Kogan, Jillene, John C. Egelhoff, & Howard M. Saal. (2008). Interstitial deletion of 13q associated with polymicrogyria. American Journal of Medical Genetics Part A. 146A(7). 910–916. 15 indexed citations
10.
Zárate, Yuri A., Jillene Kogan, Elizabeth K. Schorry, Teresa A. Smolarek, & Robert J. Hopkin. (2007). A new case of de novo 11q duplication in a patient with normal development and intelligence and review of the literature. American Journal of Medical Genetics Part A. 143A(3). 265–270. 18 indexed citations
11.
Wühl, Elke, Jillene Kogan, Aleksandra Żurowska, et al.. (2007). Neurodevelopmental deficits in Pierson (microcoria‐congenital nephrosis) syndrome. American Journal of Medical Genetics Part A. 143A(4). 311–319. 39 indexed citations
12.
Wedig, Kathy E., Jillene Kogan, Elizabeth K. Schorry, & Jeffrey A. Whitsett. (2006). Skeletal demineralization and fractures caused by fetal magnesium toxicity. Journal of Perinatology. 26(6). 371–374. 26 indexed citations
13.
VanDeVoorde, René G., David P. Witte, Jillene Kogan, & Jens Goebel. (2006). Pierson Syndrome: A Novel Cause of Congenital Nephrotic Syndrome. PEDIATRICS. 118(2). e501–e505. 31 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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