Cristopher V. Van Hout

5.2k total citations
28 papers, 509 citations indexed

About

Cristopher V. Van Hout is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Cristopher V. Van Hout has authored 28 papers receiving a total of 509 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Genetics and 3 papers in Surgery. Recurrent topics in Cristopher V. Van Hout's work include Genetic Associations and Epidemiology (9 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Genomics and Rare Diseases (4 papers). Cristopher V. Van Hout is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers) and Genomics and Rare Diseases (4 papers). Cristopher V. Van Hout collaborates with scholars based in United States, Mexico and Israel. Cristopher V. Van Hout's co-authors include Alan R. Shuldiner, Andrew G. Clark, Jesper Gromada, John D. Overton, Aris Baras, Jeffrey G. Reid, Hye In Kim, Helen H. Hobbs, Viktoria Gusarova and Sara Hamon and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Cristopher V. Van Hout

28 papers receiving 504 citations

Peers

Countries citing papers authored by Cristopher V. Van Hout

Since Specialization

Citations

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

Fields of papers citing papers by Cristopher V. Van Hout

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cristopher V. Van Hout. 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 Cristopher V. Van Hout. The network helps show where Cristopher V. Van Hout may publish in the future.

Co-authorship network of co-authors of Cristopher V. Van Hout

This figure shows the co-authorship network connecting the top 25 collaborators of Cristopher V. Van Hout. A scholar is included among the top collaborators of Cristopher V. Van Hout 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 Cristopher V. Van Hout. Cristopher V. Van Hout 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	Identification and functional validation of rare coding variants in genes linked to monogenic obesity 2024 ·Obesity ·Çiğdem Köroğlu, Michael Traurig, Yunhua L. Muller, (unknown), Paolo Piaggi, (unknown), (unknown), Robert L. Hanson, Cristopher V. Van Hout, Anna Alkelai, Alan R. Shuldiner, Clifton Bogardus, Leslie J. Baier	1
2	Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population 2023 ·Molecular Psychiatry ·Elizabeth Humphries, Kwangmi Ahn, Rachel L. Kember, Fabiana L. Lopes, Evelina Mocci, Juan M. Peralta, John Blangero, David C. Glahn, Fernando S. Goes, Peter P. Zandi, Peter Kochunov, Cristopher V. Van Hout, Alan R. Shuldiner, Toni I. Pollin, Braxton D. Mitchell, Maja Bućan, L. Elliot Hong, Francis J. McMahon, Seth A. Ament	1
3	Clinical case study meets population cohort: identification of a BRCA1 pathogenic founder variant in Orcadians 2023 ·European Journal of Human Genetics ·Shona M. Kerr, (unknown), Lucija Klarić, Christine Bell, Dawn O’Sullivan, David Buchanan, Joseph J. Grzymski, Cristopher V. Van Hout, Gannie Tzoneva, Alan R. Shuldiner, James F. Wilson, Zosia Miedzybrodzka	3
4	Functional characterization of a novel p.Ser76Thr variant in IGFBP4 that associates with body mass index in American Indians 2022 ·European Journal of Human Genetics ·Yunhua L. Muller, Michael S. Saporito, (unknown), (unknown), Çiğdem Köroğlu, Sayuko Kobes, William C. Knowler, Robert L. Hanson, Cristopher V. Van Hout, Alan R. Shuldiner, Clifton Bogardus, Leslie J. Baier	1
5	Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium 2021 ·Journal of the American Society of Nephrology ·Xuesi Wan, James A. Perry, Haichen Zhang, (unknown), Kathleen A. Ryan, Cristopher V. Van Hout, Jeffrey G. Reid, John D. Overton, Aris Baras, Zhe Han, Elizabeth A. Streeten, Yanbing Li, Braxton D. Mitchell, Alan R. Shuldiner, Mao Fu	11
6	Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals 2021 ·Genetic Epidemiology ·Chuan Gao, Anthony Marcketta, Joshua Backman, Colm O’Dushlaine, Jeffrey Staples, Manuel Allen Revez Ferreira, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Tooraj Mirshahi, Aris Baras, Gonçalo R. Abecasis, Alan R. Shuldiner, Cristopher V. Van Hout, Shane McCarthy	9
7	Genome-wide survey of parent-of-origin-specific associations across clinical traits derived from electronic health records 2021 ·SHILAP Revista de lepidopterología ·Hye In Kim, Bin Ye, Jeffrey Staples, Anthony Marcketta, Chuan Gao, Alan R. Shuldiner, Cristopher V. Van Hout	3
8	The burden of pathogenic variants in clinically actionable genes in a founder population 2021 ·American Journal of Medical Genetics Part A ·(unknown), Kristin A. Maloney, Toni I. Pollin, Elizabeth A. Streeten, Huichun Xu, Alan R. Shuldiner, Cristopher V. Van Hout, Claudia Gonzaga‐Jauregui, Braxton D. Mitchell	6
9	Exome Sequencing of 21 Bardet‐Biedl Syndrome (BBS) Genes to Identify Obesity Variants in 6,851 American Indians 2021 ·Obesity ·(unknown), Yunhua L. Muller, Çiğdem Köroğlu, Sayuko Kobes, (unknown), (unknown), Hye In Kim, Cristopher V. Van Hout, Nehal Gosalia, Bin Ye, Alan R. Shuldiner, William C. Knowler, Robert L. Hanson, Clifton Bogardus, Leslie J. Baier	9
10	Next generation sequencing for HLA loci in full heritage Pima Indians of Arizona, Part II: HLA-A, -B, and -C with selected non-classical loci at 4-field resolution from whole genome sequences 2021 ·Human Immunology ·Robert C. Williams, Çiğdem Köroğlu, William C. Knowler, Alan R. Shuldiner, Nehal Gosalia, Cristopher V. Van Hout, Robert L. Hanson, Clifton Bogardus, Leslie J. Baier	1
11	Angiopoietin-like protein 3 governs LDL-cholesterol levels through endothelial lipase-dependent VLDL clearance 2020 ·Journal of Lipid Research ·Rene C. Adam, (unknown), (unknown), (unknown), (unknown), Poulabi Banerjee, Sara Hamon, Hye In Kim, Jonathan C. Cohen, Helen H. Hobbs, Cristopher V. Van Hout, Jesper Gromada, Andrew Murphy, George D. Yancopoulos, Mark W. Sleeman, Viktoria Gusarova	124
12	Leveraging phenotypic variability to identify genetic interactions in human phenotypes 2020 ·The American Journal of Human Genetics ·Andrew R. Marderstein, Emily Davenport, Scott Kulm, Cristopher V. Van Hout, Olivier Elemento, Andrew G. Clark	38
13	Assessment of the potential role of natural selection in type 2 diabetes and related traits across human continental ancestry groups: comparison of phenotypic with genotypic divergence 2020 ·Diabetologia ·Robert L. Hanson, Cristopher V. Van Hout, Wen‐Chi Hsueh, Alan R. Shuldiner, Sayuko Kobes, Madhumita Sinha, Leslie J. Baier, William C. Knowler	4
14	Characterization of Exome Variants and Their Metabolic Impact in 6,716 American Indians from the Southwest US 2020 ·The American Journal of Human Genetics ·Hye In Kim, Bin Ye, Nehal Gosalia, Çiğdem Köroğlu, Robert L. Hanson, Wen‐Chi Hsueh, William C. Knowler, Leslie J. Baier, Clifton Bogardus, Alan R. Shuldiner, Cristopher V. Van Hout	10
15	U-PASS: unified power analysis and forensics for qualitative traits in genetic association studies 2019 ·Bioinformatics ·Zheng Gao, Jonathan Terhorst, Cristopher V. Van Hout, Stilian Stoev	1
16	Next generation sequencing and the classical HLA loci in full heritage Pima Indians of Arizona: Defining the core HLA variation for North American Paleo-Indians 2019 ·Human Immunology ·Robert C. Williams, William C. Knowler, Alan R. Shuldiner, Nehal Gosalia, Cristopher V. Van Hout, Robert L. Hanson, Clifton Bogardus, Leslie J. Baier	12
17	Genomic diagnostics within a medically underserved population: efficacy and implications 2017 ·Genetics in Medicine ·Kevin A. Strauss, Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, Katie B. Williams, Alejandra King, Cristopher V. Van Hout, (unknown), Millie Young, Kavita Praveen, (unknown), (unknown), Aris Baras, Jeffrey G. Reid, John D. Overton, Frederick E. Dewey, Robert N. Jinks, (unknown), Scott Mellis, Alan R. Shuldiner, Erik G. Puffenberger	36
18	Determinants of Blood Pressure Response to Low‐Salt Intake in a Healthy Adult Population 2011 ·Journal of Clinical Hypertension ·May E. Montasser, Julie A. Douglas, Marie‐Hélène Roy‐Gagnon, Cristopher V. Van Hout, (unknown), Robert A. Vogel, Afshin Parsa, Nanette Steinle, Søren Snitker, Nga Brereton, (unknown), Alan R. Shuldiner, Braxton D. Mitchell	21
19	Extent and distribution of linkage disequilibrium in the Old Order Amish 2009 ·Genetic Epidemiology ·Cristopher V. Van Hout, Albert M. Levin, Evadnie Rampersaud, Haiqing Shen, Jeffrey R. O’Connell, Braxton D. Mitchell, Alan R. Shuldiner, Julie A. Douglas	7
20	Long-term RNA interference from optimized siRNA expression constructs in adult mice 2005 ·Biochemical and Biophysical Research Communications ·Christine I. Wooddell, Cristopher V. Van Hout, (unknown), David L. Lewis, Hans Herweijer	23

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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