David B. Goldstein

70.4k total citations · 11 hit papers
276 papers, 27.1k citations indexed

About

David B. Goldstein is a scholar working on Genetics, Molecular Biology and Hepatology. According to data from OpenAlex, David B. Goldstein has authored 276 papers receiving a total of 27.1k indexed citations (citations by other indexed papers that have themselves been cited), including 134 papers in Genetics, 96 papers in Molecular Biology and 23 papers in Hepatology. Recurrent topics in David B. Goldstein's work include Genomics and Rare Diseases (48 papers), Genetic Associations and Epidemiology (43 papers) and Genomic variations and chromosomal abnormalities (29 papers). David B. Goldstein is often cited by papers focused on Genomics and Rare Diseases (48 papers), Genetic Associations and Epidemiology (43 papers) and Genomic variations and chromosomal abnormalities (29 papers). David B. Goldstein collaborates with scholars based in United States, United Kingdom and Australia. David B. Goldstein's co-authors include Elizabeth T. Cirulli, Kevin V. Shianna, Dongliang Ge, John G. McHutchison, Erin L. Heinzen, L. L. Cavalli‐Sforza, Anna C. Need, Jacques Fellay, Thomas Urban and Alexander Thompson and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

David B. Goldstein

268 papers receiving 26.3k citations

Hit Papers

5 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.

Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance

2009 2.6k citations Kevin V. Shianna, Thomas Urban et al. profile →
Genome-wide association studies for complex traits: consensus, uncertainty and challenges

2008 1.9k citations David B. Goldstein et al. Nature Reviews Genetics profile →
Genetic variation in IL28B and spontaneous clearance of hepatitis C virus

2009 1.6k citations John G. McHutchison, David B. Goldstein et al. profile →
An evaluation of genetic distances for use with microsatellite loci.

1995 803 citations David B. Goldstein et al. Genetics profile →
Uncovering the roles of rare variants in common disease through whole-genome sequencing

2010 777 citations David B. Goldstein et al. Nature Reviews Genetics profile →
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin

2009 732 citations David B. Goldstein et al. profile →
Genetic absolute dating based on microsatellites and the origin of modern humans.

1995 636 citations David B. Goldstein et al. Proceedings of the National Academy of Sciences profile →
Common Genetic Variation and Human Traits

2009 614 citations David B. Goldstein profile →
Rare Variants Create Synthetic Genome-Wide Associations

2010 611 citations David B. Goldstein et al. profile →
Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes

2013 546 citations Slavé Petrovski, Quanli Wang et al. PLoS Genetics profile →
A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci

2009 480 citations Kevin V. Shianna, David B. Goldstein et al. PLoS Genetics profile →

Peers

Countries citing papers authored by David B. Goldstein

Since Specialization

Citations

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

Fields of papers citing papers by David B. Goldstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David B. Goldstein. 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 David B. Goldstein. The network helps show where David B. Goldstein may publish in the future.

Co-authorship network of co-authors of David B. Goldstein

This figure shows the co-authorship network connecting the top 25 collaborators of David B. Goldstein. A scholar is included among the top collaborators of David B. Goldstein 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 David B. Goldstein. David B. Goldstein 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	Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor 2023 ·Frontiers in Cellular Neuroscience ·Sophie Colombo, (unknown), Sabrina Petri, Damian J. Williams, (unknown), Ryan S. Dhindsa, Sahar Gelfman, (unknown), (unknown), (unknown), Yueqing Peng, Christopher D. Makinson, Michael J. Boland, Wayne N. Frankel, David B. Goldstein, Nathan Dascal	7
2	Investigation into the genetics of fetal congenital lymphatic anomalies 2023 ·Prenatal Diagnosis ·(unknown), Anna Alkelai, Jessica L. Giordano, (unknown), (unknown), Chia‐Ling Nhan‐Chang, Joshua E. Motelow, Vimla S. Aggarwal, David B. Goldstein, Ronald J. Wapner, Carrie J. Shawber	14
3	Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency 2023 ·PLoS Genetics ·Sarah A. Dugger, Ryan S. Dhindsa, Gabriela Louise de Almeida Sampaio, (unknown), (unknown), Sabrina Petri, Verity A. Letts, (unknown), Junqiang Ye, Sophie Colombo, Yueqing Peng, (unknown), Michael J. Boland, Wayne N. Frankel, David B. Goldstein	6
4	Ancestry adjustment improves genome-wide estimates of regional intolerance 2022 ·Genetics ·Tristan J. Hayeck, Nicholas Stong, Evan H. Baugh, Ryan S. Dhindsa, Tychele N. Turner, (unknown), Timothy L. Mosbruger, Grace Tzun-Wen Shaw, (unknown), Iuliana Ionita‐Laza, David B. Goldstein, Andrew S. Allen	2
5	Exome sequencing in obsessive–compulsive disorder reveals a burden of rare damaging coding variants 2021 ·Nature Neuroscience ·Matthew Halvorsen, Jack Samuels, Ying Wang, Benjamin D. Greenberg, Abby J. Fyer, James T. McCracken, Daniel Geller, James A. Knowles, Anthony W. Zoghbi, Tess D. Pottinger, (unknown), Mark A. Riddle, O. Joseph Bienvenu, Paul S. Nestadt, Janice Krasnow, Fernando S. Goes, Brion S. Maher, Gerald Nestadt, David B. Goldstein	36
6	Cases in Precision Medicine: Genetic Testing to Predict Future Risk for Disease in a Healthy Patient 2021 ·Annals of Internal Medicine ·Hila Milo Rasouly, Vimla S. Aggarwal, Louise Bier, David B. Goldstein, Ali G. Gharavi	4
7	High-impact rare genetic variants in severe schizophrenia 2021 ·Proceedings of the National Academy of Sciences ·Anthony W. Zoghbi, Ryan S. Dhindsa, Terry E. Goldberg, (unknown), Joshua E. Motelow, Xinchen Wang, Anna Alkelai, Matthew Harms, Jeffrey A. Lieberman, Sander Markx, David B. Goldstein	33
8	Rare-variant collapsing analyses for complex traits: guidelines and applications 2019 ·Nature Reviews Genetics ·Gundula Povysil, Slavé Petrovski, Joseph Hostyk, Vimla S. Aggarwal, Andrew S. Allen, David B. Goldstein	109
9	Sudden unexpected death in asymptomatic infants due to PPA2 variants 2019 ·Molecular Genetics & Genomic Medicine ·Colin K. L. Phoon, Matthew Halvorsen, David B. Goldstein, Rachel Rabin, Frank Cecchin, Laura Gould, Orrin Devinsky	20
10	meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays 2018 ·PLoS Computational Biology ·Sahar Gelfman, Quanli Wang, Yifan Lu, (unknown), Christopher D. Bostick, Ryan S. Dhindsa, Matthew Halvorsen, K. Melodi McSweeney, (unknown), (unknown), Michael Beaumont, Wayne N. Frankel, Slavé Petrovski, Andrew S. Allen, Michael J. Boland, David B. Goldstein, Stephen J. Eglen	19
11	Annotating pathogenic non-coding variants in genic regions 2017 ·Nature Communications ·Sahar Gelfman, Quanli Wang, K. Melodi McSweeney, Zhong Ren, Francesca La Carpia, Matthew Halvorsen, Kelly Schoch, (unknown), Erin L. Heinzen, Michael J. Boland, Slavé Petrovski, David B. Goldstein	99
12	Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics 2017 ·PLoS ONE ·Ayal B. Gussow, Brett Copeland, Ryan S. Dhindsa, Quanli Wang, Slavé Petrovski, William H. Majoros, Andrew S. Allen, David B. Goldstein	135
13	A nonsense mutation in IKBKB causes combined immunodeficiency 2014 ·Blood ·Talal Mousallem, Jialong Yang, Thomas Urban, Hongxia Wang, Mehdi Adeli, Roberta Parrott, Joseph L. Roberts, David B. Goldstein, Rebecca H. Buckley, Xiao-Ping Zhong	43
14	Psychosocial outcomes in first-generation immigrant cancer patients in Australia 2012 ·The Sydney eScholarship Repository (The University of Sydney) ·Ming Sze, PN Butow, Melanie L. Bell, David B. Goldstein, Madeleine King, Michael Jefford, Afaf Girgis, Maurice Eisenbruch, L. Vaccaro, Skye Dong	1
15	125 IL28B POLYMORPHISM IS ASSOCIATED WITH JAUNDICE DURING ACUTE HCV INFECTION AND IS A STRONG PREDICTOR FOR SPONTANEOUS CLEARANCE IN THE PROSPECTIVE GERMAN ANTI-D COHORT 2010 ·Journal of Hepatology ·Hans L. Tillmann, Amber Thompson, Keyur Patel, (unknown), H Tenckhoff, Hans Dieter Nischalke, U. Kullig, (unknown), (unknown), Johannes Wiegand, Ingolf Schiefke, Ulrich Spengler, Jane McCarthy, Kevin V. Shianna, David B. Goldstein, John G. McHutchison, Jörg Timm, Jacob Nattermann	4
16	Testing for cytochrome P450 polymorphisms in adults with non-psychotic depression treated with selective serotonin reuptake inhibitors (SSRIs). 2007 ·PubMed ·David B. Matchar, Mugdha Thakur, Iris Grossman, Douglas C McCrory, Lori A. Orlando, David C. Steffens, David B. Goldstein, (unknown), Rebecca N Gray	50
17	Population Genetic and Phylogenetic Evidence for Positive Selection on Regulatory Mutations at the Factor VII Locus in HumansSequence data from this article have been deposited with the EMBL/GenBank Data Libraries under accession nos. AY493422, AY493423, AY493424, AY493425, AY493426, AY493427, AY493428, AY493429, AY493430, AY493431, AY493432, AY493433. 2004 ·Genetics ·Matthew W. Hahn, Matthew V. Rockman, Nicole Soranzo, David B. Goldstein, Gregory A. Wray	44
18	Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics 2003 ·Science ·Simon Mead, Michael P. H. Stumpf, Jerome Whitfield, Jonathan Beck, Mark Poulter, Tracy Campbell, (unknown), David B. Goldstein, Michael P. Alpers, Elizabeth Fisher, John Collinge	276
19	The e-healthcare cybertsunami. 2000 ·PubMed ·David B. Goldstein	1
20	National health and medical websites take off, but to where? 1999 ·PubMed ·David B. Goldstein, (unknown)	1

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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