Joseph DeYoung

5.1k total citations · 1 hit paper
22 papers, 2.0k citations indexed

About

Joseph DeYoung is a scholar working on Molecular Biology, Oncology and Clinical Biochemistry. According to data from OpenAlex, Joseph DeYoung has authored 22 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Oncology and 5 papers in Clinical Biochemistry. Recurrent topics in Joseph DeYoung's work include Drug Transport and Resistance Mechanisms (8 papers), Metabolism and Genetic Disorders (5 papers) and Genetic Associations and Epidemiology (4 papers). Joseph DeYoung is often cited by papers focused on Drug Transport and Resistance Mechanisms (8 papers), Metabolism and Genetic Disorders (5 papers) and Genetic Associations and Epidemiology (4 papers). Joseph DeYoung collaborates with scholars based in United States, Netherlands and Costa Rica. Joseph DeYoung's co-authors include Kathleen M. Giacomini, Nelson B. Freimer, Ira Herskowitz, Michiko Kawamoto, Conrad C. Huang, Thomas E. Ferrin, Susan J. Johns, Doug Stryke, Elaine J. Carlson and Travis R. Taylor and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Joseph DeYoung

21 papers receiving 1.9k 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.

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

1998 529 citations Laura N. Bull, Michiel J. T. van Eijk et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joseph DeYoung United States	15	1.0k	620	477	426	261	22	2.0k
David A. Katz United States	27	527 0.5×	1.1k 1.7×	487 1.0×	188 0.4×	309 1.2×	64	3.4k
U. Karbach Germany	20	811 0.8×	521 0.8×	255 0.5×	380 0.9×	109 0.4×	45	2.0k
Hélène Blanché France	25	198 0.2×	1.1k 1.8×	637 1.3×	254 0.6×	191 0.7×	61	3.2k
Peter Hughes Australia	23	220 0.2×	1.0k 1.7×	321 0.7×	201 0.5×	731 2.8×	84	2.8k
Toshihiro Ohura Japan	27	179 0.2×	1.5k 2.4×	351 0.7×	574 1.3×	156 0.6×	90	3.0k
Qinghe Xing China	25	250 0.2×	377 0.6×	177 0.4×	172 0.4×	117 0.4×	80	1.6k
Devorah Gurantz United States	21	556 0.6×	547 0.9×	388 0.8×	157 0.4×	206 0.8×	24	1.6k
Rui M. B. Maciel Brazil	31	307 0.3×	1.2k 1.9×	600 1.3×	148 0.3×	343 1.3×	186	3.6k
Masanobu Yamada Japan	31	435 0.4×	1.1k 1.8×	803 1.7×	58 0.1×	329 1.3×	208	3.7k
Jun Nakura Japan	25	297 0.3×	1.9k 3.0×	208 0.4×	120 0.3×	292 1.1×	71	3.2k

Countries citing papers authored by Joseph DeYoung

Since Specialization

Citations

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

Fields of papers citing papers by Joseph DeYoung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joseph DeYoung

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph DeYoung. A scholar is included among the top collaborators of Joseph DeYoung 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 Joseph DeYoung. Joseph DeYoung 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

Hilser, James R., Jaana Hartiala, Intira Sriprasert, et al.. (2022). Effect of menopausal hormone therapy on methylation levels in early and late postmenopausal women. Clinical Epigenetics. 14(1). 90–90. 3 indexed citations

Jasinska, Anna J., Amin Haghani, Joseph A. Zoller, et al.. (2021). Epigenetic clock and methylation studies in vervet monkeys. GeroScience. 44(2). 699–717. 18 indexed citations

Loohuis, Loes M. Olde, Jacob Vorstman, Anil P. S. Ori, et al.. (2015). Genome-wide burden of deleterious coding variants increased in schizophrenia. Nature Communications. 6(1). 7501–7501. 18 indexed citations

Luykx, Jurjen J., S C Bakker, Nan van Geloven, et al.. (2013). Seasonal variation of serotonin turnover in human cerebrospinal fluid, depressive symptoms and the role of the 5-HTTLPR. Translational Psychiatry. 3(10). e311–e311. 25 indexed citations

Jasinska, Anna J., Michelle K. Lin, Susan K. Service, et al.. (2012). A non-human primate system for large-scale genetic studies of complex traits. Human Molecular Genetics. 21(15). 3307–3316. 21 indexed citations

Jasinska, Anna J., Susan K. Service, Oi‐Wa Choi, et al.. (2009). Identification of brain transcriptional variation reproduced in peripheral blood: an approach for mapping brain expression traits. Human Molecular Genetics. 18(22). 4415–4427. 43 indexed citations

Saris, Christiaan G. J., Steve Horvath, Paul W.J. van Vught, et al.. (2009). Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients. BMC Genomics. 10(1). 405–405. 139 indexed citations

Kerner, Berit, et al.. (2008). Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(1). 24–32. 27 indexed citations

Service, Susan K., Júlio César Molina, Joseph DeYoung, et al.. (2008). Results of a SNP genome screen in a large Costa Rican Pedigree segregating for severe bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(4). 540–540.

10.

Service, Susan K., Julio Molina, Joseph DeYoung, et al.. (2006). Results of a SNP genome screen in a large Costa Rican pedigree segregating for severe bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(4). 367–373. 12 indexed citations

11.

Shu, Yan, Maya K. Leabman, Bo Feng, et al.. (2004). PharmGKB Update: III. Genetic Variants of SLC22A1, Solute Carrier Family 22 (Organic Cation Transporter), Member 1. Pharmacological Reviews. 56(2). 161–161. 4 indexed citations

12.

Kroetz, Deanna L., Christiane Pauli‐Magnus, Laura M. Hodges, et al.. (2003). Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene. Pharmacogenetics. 13(8). 481–494. 352 indexed citations

13.

Leabman, Maya K., Conrad C. Huang, Joseph DeYoung, et al.. (2003). Natural variation in human membrane transporter genes reveals evolutionary and functional constraints. Proceedings of the National Academy of Sciences. 100(10). 5896–5901. 180 indexed citations

14.

Leabman, Maya K., Conrad C. Huang, Doug Stryke, et al.. (2003). PharmGKB Update: I. Genetic Variants of the Organic Cation Transporter 2 (OCT2, SLC22A2). Pharmacological Reviews. 55(3). 399–399. 7 indexed citations

15.

Leabman, Maya K., Conrad C. Huang, Michiko Kawamoto, et al.. (2002). Polymorphisms in a human kidney xenobiotic transporter, OCT2, exhibit altered function. Pharmacogenetics. 12(5). 395–405. 153 indexed citations

16.

Glatt, Charles E., Joseph DeYoung, Sharon Delgado, et al.. (2001). Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes. Nature Genetics. 27(4). 435–438. 123 indexed citations

17.

Lucas, Julie L., Wolfgang Sadée, & Joseph DeYoung. (2001). Single nucleotide polymorphisms of the human M1 muscarinic acetylcholine receptor gene. PubMed. 3(4). 57–61. 10 indexed citations

18.

Ophoff, Roel A., Joseph DeYoung, Susan K. Service, et al.. (2001). Hereditary Vascular Retinopathy, Cerebroretinal Vasculopathy, and Hereditary Endotheliopathy with Retinopathy, Nephropathy, and Stroke Map to a Single Locus on Chromosome 3p21.1-p21.3. The American Journal of Human Genetics. 69(2). 447–453. 84 indexed citations

19.

Bull, Laura N., Michiel J. T. van Eijk, Ludmila Pawlikowska, et al.. (1998). A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nature Genetics. 18(3). 219–224. 529 indexed citations breakdown →

20.

Healy, Jasmine, Catherine Corr, Joseph DeYoung, & Barbara Baker. (1993). Linked and unlinked transposition of a genetically marked Dissociation element in transgenic tomato.. Genetics. 134(2). 571–584. 29 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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