David R. Beier

17.8k citations

175 papers · 13.7k indexed · 3 hit papers · h-index 58

Impact in

Genetics top 0.2%
- Genetic and Kidney Cyst Diseases
Immunology and Allergy top 0.5%

Papers in

Genetics 73
- Genetic and Kidney Cyst Diseases 30
- Animal Genetics and Reproduction 12
Immunology and Allergy 12

Co-authors: Bryan C. Bjork Dorothee Foernzler Helen Her William F. Dietrich Mark D. Fleming Cameron C. Trenor Maureen A. Su Nancy C. Andrews
Journals: Mammalian Genome (14 papers)Genomics (13 papers)Nature Genetics (6 papers)G3 Genes Genomes Genetics (5 papers)Human Molecular Genetics (5 papers)
Partner nations: United States Germany Canada

In The Last Decade

David R. Beier

174 papers receiving 13.5k citations

Hit Papers

align trajectories log scale

PRDM16 controls a brown fat/skeletal muscle switch 2008 · 1.8k citations

Peers

Countries citing papers authored by David R. Beier

Since Specialization

Citations

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

Fields of papers citing papers by David R. Beier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside David R. Beier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with David R. Beier Line = papers co-authored together David R. Beier links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defects PLoS Genetics ·Gist H. Farr, 光也細山, Elin Hidmark, Nicholas Christopher, I D Young, H Ghasemnejad, Aaron Olson, David R. Beier, Lisa Maves	2025	1
2	The arginine methyltransferaseCarm1is necessary for heart development G3 Genes Genomes Genetics ·Dewei Liu, Seungshin Ha, D Wiwattamongkol, Scott Houghtaling, Andrew E. Timms, Kai Yu, Alison G. Paquette, A. Murat Maga, Nicholas D. E. Greene, David R. Beier	2022	4
3	Applicability of the Mutation–Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in Humans Molecular Biology and Evolution ·Donate Weghorn, Daniel J. Balick, Christopher A. Cassa, Jack A. Kosmicki, Mark J. Daly, David R. Beier, Shamil Sunyaev	2019	15
4	Generation of a multipurpose Prdm16 mouse allele by targeted gene trapping Disease Models & Mechanisms ·R. Madjoe, Frank Schnütgen, Qi Dai, Jennifer Jones, Angela C. Gomez, Mohd Hilmi bin Ramli, Nathan E. Holton, О. Ю. Фетисова, 直践河野, Harald von Melchner, David R. Beier, Bryan C. Bjork	2017	10
5	Mutation of the BiP/GRP78 gene causes axon outgrowth and fasciculation defects in the thalamocortical connections of the mammalian forebrain The Journal of Comparative Neurology ·Mulas, Li Senxi, Cynthia M. Grimsley‐Myers, 武田鐡治郎, David R. Beier, Noelle D. Dwyer	2012	18
6	The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch Proceedings of the National Academy of Sciences ·Nathan E. Hellman, Yan Liu, Erin Merkel, Christina Austin‐Tse, Stéphanie Le Corre, David R. Beier, Zhaoxia Sun, Neeraj Sharma, Bradley K. Yoder, Iain A. Drummond	2010	66
7	Genome-wide identification of mouse congenital heart disease loci Human Molecular Genetics ·Anna Kamp, Michael Peterson, Karen L. Svenson, Bryan C. Bjork, Kathryn E. Hentges, Tharinda W. Rajapaksha, Jennifer L. Moran, Monica J. Justice, J.G. Seidman, Christine E. Seidman, Ivan P. Moskowitz, David R. Beier	2010	15
8	Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210 New England Journal of Medicine ·Patrick Smits, Andrew D. Bolton, Vincent Funari, Ángel Valés-Vázquez, Mikhail V. Vinogradov, Lei Lü, Danielle K. Manning, Noelle D. Dwyer, Jennifer L. Moran, Caifa You, Barry Merriman, Stanley F. Nelson, Luisa Bonafé, Andrea Superti‐Furga, Shiro Ikegawa, Deborah Krakow, Daniel H. Cohn, Tomas Kirchhausen, Matthew L. Warman, David R. Beier	2010	106
9	A Transient Transgenic RNAi Strategy for Rapid Characterization of Gene Function during Embryonic Development PLoS ONE ·Bryan C. Bjork, Yuko Fujiwara, Shannon W. Davis, Haiyan Qiu, Thomas L. Saunders, Péter Sandy, Stuart H. Orkin, Sally A. Camper, David R. Beier	2010	13
10	Utilization of a whole genome SNP panel for efficient genetic mapping in the mouse Genome Research ·Jennifer L. Moran, Andrew D. Bolton, Pamela V. Tran, Alison Brown, Noelle D. Dwyer, Danielle K. Manning, Bryan C. Bjork, Cheng Li, Kate Montgomery, Sandra M. Siepka, Martha Hotz Vitaterna, Joseph S. Takahashi, Tim Wiltshire, David J. Kwiatkowski, Raju Kucherlapati, David R. Beier	2006	75
11	Impaired homeostasis and phenotypic abnormalities in Prdx6−/−mice lens epithelial cells by reactive oxygen species: increased expression and activation of TGFβ Cell Death and Differentiation ·F Li, Eri Kubo, Preeti Sharma, David R. Beier, Dhirendra P. Singh	2005	81
12	Cordon-bleu is a conserved gene involved in neural tube formation Developmental Biology ·Friedrich Lohr, Dianne Gerrelli, Stéphan Gasca, Elizabeth L. Berg, David R. Beier, Andrew J. Copp, John Klingensmith	2003	73
13	Characterization of the Murine Lbx2 Promoter, Identification of the Human Homologue, and Evaluation as a Candidate for Alström Syndrome Genomics ·Fabian Chen, Gayle B. Collin, Kenneth C. Liu, David R. Beier, Michael R. Eccles, Patsy M. Nishina, Kever Bruno Paradelo Gomes, Jonathan A. Epstein	2001	5
14	Cloning and Expression of a Murine Histone Deacetylase 3 (mHdac3) cDNA and Mapping to a Region of Conserved Synteny between Murine Chromosome 18 and Human Chromosome 5 PubMed ·Fernando Dangond, ชุรีภรณ์ โมทารัตน์, Stanislawa Weremowicz, Naufal Hartanto, David R. Beier, Steven R. Gullans	1999	8
15	A Novel Putative Transporter Maps to the Osteosclerosis (oc) Mutation and Is Not Expressed in theocMutant Mouse Genomics ·義也経塚, Holly Dushkin, Rosana Santos de Albuquerque, Tatsuya Koike, N. V. S. Sastri, Helen Her, Steven R. Gullans, Gino V. Segre, Richard M. Green, David R. Beier	1999	67
16	The spontaneous coat color mutant white nose ( wn ) maps to murine Chromosome 15 Mammalian Genome ·Peter Marks, Hangjia Lu, Dar-Bin Shieh, Dorothee Foernzler, David R. Beier, Fabián Camilo Peña Perilla	1999	2
17	Genetic Analysis of a Quantitative Trait in a Mouse Model of Polycystic Kidney Disease American Journal of Respiratory and Critical Care Medicine ·Olga A. Iakoubova, Holly Dushkin, David R. Beier	1997	16
18	Conservation of dishevelled structure and function between flies and mice: isolation and characterization of Dvl2 Mechanisms of Development ·John Klingensmith, A ARTEGIANI, Jeffrey D. Axelrod, David R. Beier, Norbert Perrimon, Daniel J. Sussman	1996	95
19	Genetics of pattern formation and growth control The American Journal of Human Genetics ·David R. Beier	1991	46
20	Perinatal lethality (ple): A mutation caused by integration of a transgene into distal mouse chromosome 15 Genomics ·David R. Beier, Cynthia C. Morton, Aya Leder, Zhengrui Shi, Philip Leder	1989	18

About David R. Beier

David R. Beier is a scholar working on Genetics, Immunology and Allergy, Molecular Biology, Cell Biology and Developmental Neuroscience, having authored 175 papers that have together received 13.7k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (30 papers), Renal and related cancers (25 papers), Genomics and Chromatin Dynamics (16 papers), Epigenetics and DNA Methylation (16 papers), RNA Research and Splicing (15 papers), CRISPR and Genetic Engineering (14 papers), Hedgehog Signaling Pathway Studies (12 papers) and Animal Genetics and Reproduction (12 papers). The work is most often cited by research in Genetics (3.4k citations), Immunology and Allergy (643 citations), Cell Biology (1.7k citations), Molecular Biology (7.1k citations) and Immunology (2.1k citations). David R. Beier has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Bryan C. Bjork, Dorothee Foernzler, Helen Her, William F. Dietrich, Mark D. Fleming, Cameron C. Trenor, Maureen A. Su, Nancy C. Andrews, Michael A. Rudnicki and Wenli Yang. Their work appears in journals such as Mammalian Genome, Genomics, Nature Genetics, G3 Genes Genomes Genetics and Human Molecular Genetics.

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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