Kelly Gonzalez

1.5k total citations
18 papers, 943 citations indexed

About

Kelly Gonzalez is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Kelly Gonzalez has authored 18 papers receiving a total of 943 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Kelly Gonzalez's work include Cancer Genomics and Diagnostics (5 papers), Genomics and Rare Diseases (4 papers) and Genomics and Chromatin Dynamics (4 papers). Kelly Gonzalez is often cited by papers focused on Cancer Genomics and Diagnostics (5 papers), Genomics and Rare Diseases (4 papers) and Genomics and Chromatin Dynamics (4 papers). Kelly Gonzalez collaborates with scholars based in United States, Canada and China. Kelly Gonzalez's co-authors include Steve S. Sommer, Dongqing Gu, Katrina Lowstuter, Jeffrey N. Weitzel, Jeff Longmate, Vũ Quốc Huy Nguyễn, Carolyn H. Buzin, Jennifer Han, Sha Tang and Layla Shahmirzadi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Neurology.

In The Last Decade

Kelly Gonzalez

18 papers receiving 921 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kelly Gonzalez United States	13	423	413	267	248	110	18	943
Ana Novokmet Canada	11	355 0.8×	582 1.4×	472 1.8×	444 1.8×	161 1.5×	15	1.3k
Nayanta Sodha United Kingdom	13	341 0.8×	692 1.7×	521 2.0×	257 1.0×	175 1.6×	21	1.1k
Pamela J. Reitnauer United States	11	395 0.9×	539 1.3×	249 0.9×	224 0.9×	123 1.1×	20	1.1k
A M van den Ouweland Netherlands	13	286 0.7×	312 0.8×	122 0.5×	186 0.8×	52 0.5×	19	737
Bernard Peissel Italy	21	948 2.2×	942 2.3×	253 0.9×	208 0.8×	265 2.4×	63	1.7k
David Malkin Canada	20	214 0.5×	481 1.2×	370 1.4×	208 0.8×	189 1.7×	48	1.3k
Robert Huether United States	14	597 1.4×	423 1.0×	187 0.7×	295 1.2×	219 2.0×	30	1.0k
Seval Türkmen Germany	17	474 1.1×	752 1.8×	147 0.6×	98 0.4×	44 0.4×	36	1.3k
Jenny Lester United States	15	140 0.3×	335 0.8×	239 0.9×	234 0.9×	65 0.6×	26	868
Cheryl L. Soderberg United States	8	568 1.3×	262 0.6×	196 0.7×	348 1.4×	187 1.7×	9	873

Countries citing papers authored by Kelly Gonzalez

Since Specialization

Citations

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

Fields of papers citing papers by Kelly Gonzalez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kelly Gonzalez

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

All Works

Sort: Min cites: Since: Top N: Style:

18 of 18 papers shown

Way, Charles W. Van, et al.. (2019). Metabolic Support for 40 years at a University Hospital. Nutrition in Clinical Practice. 34(6). 802–805. 1 indexed citations

Tang, Sha, Russell S. Miller, Luis Rohena, et al.. (2015). New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome). Fetal Diagnosis and Therapy. 38(4). 296–306. 40 indexed citations

Basel‐Vanagaite, Lina, Rüstem Yilmaz, Sha Tang, et al.. (2014). Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations. Human Genetics. 133(7). 939–949. 28 indexed citations

Butterfield, Russell J., Tamara J. Stevenson, Lingyan Xing, et al.. (2014). Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis. Neurology. 82(15). 1322–1330. 43 indexed citations

Gonzalez, Kelly, Hsiao‐Mei Lu, Hong Lu, et al.. (2014). Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 Genes. JIMD Reports. 15. 29–37. 9 indexed citations

Yu, Lan, Wenqi Zeng, Xiang Li, et al.. (2013). A human de novo mutation inMYH10phenocopies the loss of function mutation in mice. PubMed. 1(1). e26144–e26144. 32 indexed citations

Rohena, Luis, Julie Neidich, Kelly Gonzalez, et al.. (2013). Mutation inSNAP25as a novel genetic cause of epilepsy and intellectual disability. PubMed. 1(1). e26314–e26314. 53 indexed citations

Shahmirzadi, Layla, et al.. (2013). Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing. Genetics in Medicine. 16(5). 395–399. 89 indexed citations

Gandomi, Stephanie, Kelly Gonzalez, Layla Shahmirzadi, et al.. (2013). Diagnostic Exome Sequencing Identifies Two Novel IQSEC2 Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis. Journal of Genetic Counseling. 23(3). 289–298. 35 indexed citations

10.

Gonzalez, Kelly, Carolyn H. Buzin, Dongqing Gu, et al.. (2009). Beyond Li Fraumeni Syndrome: Clinical Characteristics of Families With p53 Germline Mutations. Journal of Clinical Oncology. 27(8). 1250–1256. 391 indexed citations

11.

Scaringe, William A., Kai Li, Dongqing Gu, et al.. (2008). Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates. Human Molecular Genetics. 17(18). 2910–2918. 10 indexed citations

12.

Gonzalez, Kelly, Cindy Fong, Carolyn H. Buzin, Steve S. Sommer, & Juan‐Sebastian Saldivar. (2008). p53 Testing for Li‐Fraumeni and Li‐Fraumeni‐Like Syndromes. Current Protocols in Human Genetics. 57(1). Unit 10.10–Unit 10.10. 3 indexed citations

13.

Wang, Jicheng, Kelly Gonzalez, William A. Scaringe, et al.. (2007). Evidence for mutation showers. Proceedings of the National Academy of Sciences. 104(20). 8403–8408. 56 indexed citations

14.

Gu, Dongqing, William A. Scaringe, Kai Li, et al.. (2007). Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature. Human Mutation. 28(8). 760–770. 46 indexed citations

15.

Gonzalez, Kelly, Kathleen A. Hill, Kai Li, et al.. (2006). Somatic microindels: analysis in mouse soma and comparison with the human germline. Human Mutation. 28(1). 69–80. 15 indexed citations

16.

Ricker, Charité, Veronica I. Lagos, Nancy Feldman, et al.. (2006). If We Build It … Will They Come? – Establishing a Cancer Genetics Services Clinic for an Underserved Predominantly Latina Cohort. Journal of Genetic Counseling. 15(6). 505–514. 56 indexed citations

17.

Hill, Kathleen A., Kelly Gonzalez, Jeff Longmate, et al.. (2005). Tissue-specific time courses of spontaneous mutation frequency and deviations in mutation pattern are observed in middle to late adulthood in Big Blue mice. Environmental and Molecular Mutagenesis. 45(5). 442–454. 29 indexed citations

18.

Hill, Kathleen A., Kelly Gonzalez, William A. Scaringe, Jicheng Wang, & Steve S. Sommer. (2005). Preferential occurrence of 1-2 microindels. Human Mutation. 27(1). 55–61. 7 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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