Andrew D. Skol

19.0k total citations · 1 hit paper
56 papers, 2.3k citations indexed

About

Andrew D. Skol is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Andrew D. Skol has authored 56 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 16 papers in Molecular Biology and 9 papers in Cancer Research. Recurrent topics in Andrew D. Skol's work include Genetic Associations and Epidemiology (15 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers) and Genetic and phenotypic traits in livestock (6 papers). Andrew D. Skol is often cited by papers focused on Genetic Associations and Epidemiology (15 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers) and Genetic and phenotypic traits in livestock (6 papers). Andrew D. Skol collaborates with scholars based in United States, United Kingdom and Spain. Andrew D. Skol's co-authors include Michael Boehnke, Gonçalo R. Abecasis, Laura J. Scott, Abraham A. Palmer, Kenan Onel, Julie A. Douglas, Mark Abney, Riyan Cheng, Mark M. Sasaki and Ajna Hamidovic and has published in prestigious journals such as Nature Medicine, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Andrew D. Skol

53 papers receiving 2.3k citations

Hit Papers

align trajectories

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.

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

2006 823 citations Andrew D. Skol, Laura J. Scott et al. profile →

Peers

Countries citing papers authored by Andrew D. Skol

Since Specialization

Citations

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

Fields of papers citing papers by Andrew D. Skol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew D. Skol. 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 Andrew D. Skol. The network helps show where Andrew D. Skol may publish in the future.

Co-authorship network of co-authors of Andrew D. Skol

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew D. Skol. A scholar is included among the top collaborators of Andrew D. Skol 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 Andrew D. Skol. Andrew D. Skol 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

#	Work	Indexed citations
1	Network Analysis to Define Pediatric Acute Care Regions in Wisconsin 2025 ·Health Services Research ·Kenneth A. Michelson, Katherine Remick, Emily M. Bucholz, Patrick D. McMullen, (unknown), Andrew D. Skol, David A. Cory, John A. Graves	2
2	Out-of-State Acute Care Use Among Pediatric Medicaid Enrollees 2025 ·JAMA Network Open ·Kenneth A. Michelson, (unknown), Andrew D. Skol, Katherine Remick, Emily M. Bucholz, John A. Graves, David A. Cory, Patrick D. McMullen	0
3	A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain—Case Report and Literature Review 2024 ·Genes ·(unknown), Kai Lee Yap, (unknown), (unknown), Alexander Ing, Allan Gordon, Andrew D. Skol, Patrick D. McMullen, Brenda L. Bohnsack, Sudhi P. Kurup, Hantamalala Ralay Ranaivo, (unknown)	0
4	Genetic changes associated with relapse in favorable histology Wilms tumor: A Children’s Oncology Group AREN03B2 study 2022 ·Cell Reports Medicine ·Samantha Gadd, Vicki Huff, Andrew D. Skol, Lindsay A. Renfro, Conrad V. Fernandez, Elizabeth A. Mullen, Corbin D. Jones, Katherine A. Hoadley, Kai Lee Yap, Nilsa C. Ramirez, Sheena M. Aris, Quy H. Phung, Elizabeth J. Perlman	12
5	PIK3R5 genetic predictors of hypertension induced by VEGF-pathway inhibitors 2021 ·The Pharmacogenomics Journal ·Júlia C.F. Quintanilha, Alessandro Racioppi, Jin Wang, Amy S. Etheridge, (unknown), Carol E. Peña, Andrew D. Skol, Daniel J. Crona, D. Y. Lin, Federico Innocenti	6
6	Functional Common and Rare ERBB2 Germline Variants Cooperate in Familial and Sporadic Cancer Susceptibility 2021 ·Cancer Prevention Research ·Riyue Bao, (unknown), Mark M. Sasaki, Myvizhi Esai Selvan, Alyna Katti, (unknown), Lei Huang, Andrew D. Skol, Cinzia Lavarino, S.P. Hector, Robert J. Klein, Zeynep H. Gümüş, (unknown), Kenan Onel	2
7	Genetic Variants of VEGFA and FLT4 Are Determinants of Survival in Renal Cell Carcinoma Patients Treated with Sorafenib 2018 ·Cancer Research ·Daniel J. Crona, Andrew D. Skol, Veli‐Matti Leppänen, Dylan M. Glubb, Amy S. Etheridge, Eleanor Hilliard, Carol E. Peña, Yuri K. Peterson, Nancy Klauber‐DeMore, Kari Alitalo, Federico Innocenti	25
8	Does MAOA increase susceptibility to prenatal stress in young children? 2017 ·Neurotoxicology and Teratology ·Suena H. Massey, (unknown), Caron A. C. Clark, James Burns, Daniel S. Pine, Andrew D. Skol, Daniel K. Mroczek, Kimberly Andrews Espy, David Goldman, Edwin H. Cook, Lauren S. Wakschlag	7
9	Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma 2017 ·PLoS ONE ·Imge Hulur, Andrew D. Skol, Eric R. Gamazon, Nancy J. Cox, Kenan Onel	8
10	A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia 2017 ·Cancer Management and Research ·Russell Bainer, Matthew R. Trendowski, Cheng Cheng, Deqing Pei, Wenjian Yang, Steven W. Paugh, Kathleen H. Goss, Andrew D. Skol, Paul Pavlidis, Ching‐Hon Pui, T. Conrad Gilliam, William E. Evans, Kenan Onel	5
11	The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance 2016 ·Breast Cancer Research ·Andrew D. Skol, Mark M. Sasaki, Kenan Onel	60
12	Integrated Genomic Analysis Suggests MLL3 Is a Novel Candidate Susceptibility Gene for Familial Nasopharyngeal Carcinoma 2015 ·Cancer Epidemiology Biomarkers & Prevention ·Mark M. Sasaki, Andrew D. Skol, Riyue Bao, Lindsay Rhodes, Rachelle Chambers, Everett E. Vokes, Ezra E.W. Cohen, Kenan Onel	11
13	Do dopamine gene variants and prenatal smoking interactively predict youth externalizing behavior? 2013 ·Neurotoxicology and Teratology ·(unknown), Brian Mustanski, Andrew D. Skol, Edwin H. Cook, Lauren S. Wakschlag	13
14	Genetic Associations in the Vitamin D Receptor and Colorectal Cancer in African Americans and Caucasians 2011 ·PLoS ONE ·Sonia S. Kupfer, Jeffrey R. Anderson, Anton E. Ludvik, Stanley Hooker, Andrew D. Skol, Rick A. Kittles, Temitope O. Keku, Robert S. Sandler, Clara Ruíz-Ponte, Sergi Castellvı́-Bel, Antoni Castells, Ãngel Carracedo, Nathan A. Ellis	14
15	Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior 2009 ·Molecular Psychiatry ·Lauren S. Wakschlag, Emily O. Kistner, Daniel S. Pine, Gretchen Biesecker, Kate E. Pickett, Andrew D. Skol, Vanja Dukić, James Blair, Bennett Leventhal, Nancy J. Cox, James Burns, Kristen Kasza, R. J. Wright, Edwin H. Cook	102
16	Novel single nucleotide polymorphism associations with colorectal cancer on chromosome 8q24 in African and European Americans 2009 ·Carcinogenesis ·Sonia S. Kupfer, (unknown), Stanley Hooker, Jeffrey R. Anderson, Andrew D. Skol, Nathan A. Ellis, Rick A. Kittles	26
17	Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: An exploratory study with d-amphetamine in healthy participants. 2009 ·Experimental and Clinical Psychopharmacology ·Ajna Hamidovic, Andrea Dlugos, Andrew D. Skol, Abraham A. Palmer, Harriet de Wit	94
18	Common non-coding SNPs near the Hepatocyte Nuclear Factor-4 Alpha gene are associated with type 2 diabetes 2003 ·The American Journal of Human Genetics ·Karen L. Mohlke, Kaisa Silander, (unknown), Laura J. Scott, Pablo E. Hollstein, Andrew D. Skol, (unknown), Peter S. Chines, T. T. Valle, Richard N. Bergman, J. Tuomilehto, Richard M. Watanabe, Michael Boehnke, Francis S. Collins	2
19	Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample 2002 ·American Journal of Medical Genetics ·Stephen V. Faraone, Andrew D. Skol, Debby W. Tsuang, Stephen F. Bingham, Keith A. Young, (unknown), (unknown), (unknown), (unknown), (unknown), John Pepple, (unknown), (unknown), David M. Weiss, Joseph F. Collins, Tim P. Keith, Michael Boehnke, Ming T. Tsuang, Gerard D. Schellenberg	27
20	Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large veterans affairs cooperative study sample 2002 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Andrew D. Skol, Keith A. Young, Debby W. Tsuang, Stephen V. Faraone, (unknown), S Bingham, (unknown), (unknown), (unknown), Chang‐En Yu, (unknown), John Pepple, (unknown), (unknown), David M. Weiss, Joseph F. Collins, Tim P. Keith, Michael Boehnke, Gerald D. Schellenberg, Ming T. Tsuang	27

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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