Karynne Patterson

5.5k total citations
10 papers, 223 citations indexed

About

Karynne Patterson is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Karynne Patterson has authored 10 papers receiving a total of 223 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Karynne Patterson's work include Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Karynne Patterson is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Karynne Patterson collaborates with scholars based in United States, Australia and Estonia. Karynne Patterson's co-authors include Deborah A. Nickerson, Sean McGee, Seung‐been Lee, Andrea Gaedigk, Erica L. Woodahl, Michael J. Bamshad, Rachel Dalton, Kenneth E. Thummel, Marsha M. Wheeler and Margarita Sáenz and has published in prestigious journals such as Genetics in Medicine, Genome Medicine and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Karynne Patterson

8 papers receiving 221 citations

Peers

Countries citing papers authored by Karynne Patterson

Since Specialization

Citations

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

Fields of papers citing papers by Karynne Patterson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karynne Patterson

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities 2024 ·Communications Biology ·Eric Venner, Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla, Bo Yuan, Jason H. Karnes, Kimberly Walker, Joshua D. Smith, Sean McGee, Aparna Radhakrishnan, (unknown), Philip E. Empey, Qiaoyan Wang, Lee Lichtenstein, Diana Toledo, Gail P. Jarvik, Anjene Musick, Richard A. Gibbs, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	25
2	Using multiplexed functional data to reduce variant classification inequities in underrepresented populations 2024 ·Genome Medicine ·Moez Dawood, Shawn Fayer, Sriram Pendyala, (unknown), Divya Kalra, Karynne Patterson, Eric Venner, Lara A. Muffley, Douglas M. Fowler, Alan F. Rubin, Jennifer E. Posey, Sharon E. Plon, James R. Lupski, Richard A. Gibbs, Lea M. Starita, Carla Daniela Robles‐Espinoza, Willow Coyote‐Maestas, Irene Gallego Romero	7
3	Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome 2024 ·Genetics in Medicine ·Clémence Vanlerberghe, (unknown), Frédéric Frénois, Emilie Ait‐Yahya, (unknown), Anne Dieux, (unknown), (unknown), Sylvie Manouvrier‐Hanu, Karynne Patterson, Jamal Ghoumid, Fabienne Escande, Thomas Smol, Perrine Brunelle, Florence Petit	0
4	Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score 2024 ·Genetic Epidemiology ·Elisabeth A. Rosenthal, Li Hsu, Minta Thomas, Ulrike Peters, Christopher Kachulis, Karynne Patterson, Gail P. Jarvik	0
5	CFAP47 is Implicated in X-Linked Polycystic Kidney Disease 2024 ·Kidney International Reports ·Takayasu Mori, Takuya Fujimaru, Chunyu Liu, Karynne Patterson, Kouhei Yamamoto, Takefumi Suzuki, Motoko Chiga, Akinari Sekine, Yoshifumi Ubara, Danny E. Miller, (unknown), Shintaro Mandai, Fumiaki Ando, Yutaro Mori, Hiroaki Kikuchi, Koichiro Susa, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
6	Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome 2023 ·GeroScience ·Fuki M. Hisama, (unknown), Julia M. Sidorova, Karynne Patterson, (unknown), (unknown), Junko Oshima	2
7	Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model 2018 ·Genetics in Medicine ·Seung‐been Lee, Marsha M. Wheeler, Karynne Patterson, Sean McGee, Rachel Dalton, Erica L. Woodahl, Andrea Gaedigk, Kenneth E. Thummel, Deborah A. Nickerson	81
8	Sequencing of sporadic Attention‐Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder 2017 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Daniel Seung Kim, Amber Burt, Jane Ranchalis, Beth Wilmot, Joshua D. Smith, Karynne Patterson, Bradley P. Coe, (unknown), Michael J. Bamshad, (unknown), Evan E. Eichler, James M. Swanson, Joel T. Nigg, Deborah A. Nickerson, Gail P. Jarvik	27
9	Copy Number Changes Identified Using Whole Exome Sequencing in Nonsyndromic Cleft Lip and Palate in a Honduran Population 2017 ·Birth Defects Research ·Yi Cai, Karynne Patterson, Frédéric Reinier, (unknown), Elizabeth Blue, Michael J. Bamshad, Joseph Haddad	11
10	Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features 2015 ·Genetics in Medicine ·Jessica X. Chong, Joon‐Ho Yu, Peter Lorentzen, Karen M. Park, Seema M. Jamal, Holly K. Tabor, Anita Rauch, Margarita Sáenz, Eugen Boltshauser, Karynne Patterson, Deborah A. Nickerson, Michael J. Bamshad	69

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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