David M. Reynolds

7.2k citations

35 papers · 3.7k indexed · 1 hit paper · h-index 22

Co-authors: Stefan Somlo Guanqing Wu Yiqiang Cai Tomohito Hayashi Toshio Mochizuki Stephen Dalton Dorien J.M. Peters Barbera Veldhuisen
Topics: Genetic and Kidney Cyst Diseases (12 papers)Renal and related cancers (11 papers)Genetic Syndromes and Imprinting (9 papers)
Cited by: Genetics Molecular Biology Pathology and Forensic Medicine
Journals: Science Cell Nucleic Acids Research
Partner nations: United States Germany Spain

In The Last Decade

David M. Reynolds

34 papers receiving 3.6k 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.

PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein

1996 1.1k citations Toshio Mochizuki, Guanqing Wu et al. profile →

Peers

Countries citing papers authored by David M. Reynolds

Since Specialization

Citations

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

Fields of papers citing papers by David M. Reynolds

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David M. Reynolds

This figure shows the co-authorship network connecting the top 25 collaborators of David M. Reynolds. A scholar is included among the top collaborators of David M. Reynolds 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 M. Reynolds. David M. Reynolds 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	Prenatal vitamin D deficiency exposure leads to long-term changes in immune cell proportions 2024 ·Scientific Reports ·Koki Ueda,(unknown),Noriko Sato,Miyu Nishikawa,Kaori Yasuda,Naoyuki Miyasaka,(unknown),Laurent Chorro,(unknown),Wade Koba,David M. Reynolds,Ulrich Steidl,Grégoire Lauvau,John M. Greally,Masako Suzuki	1
2	An optimized approach for multiplexing single-nuclear ATAC-seq using oligonucleotide-conjugated antibodies 2023 ·Epigenetics & Chromatin ·(unknown),(unknown),(unknown),Hiroko Nomaru,David M. Reynolds,Robert Dubin,Shahina B. Maqbool,Deyou Zheng,Bernice E. Morrow,John M. Greally,Masako Suzuki	2
3	Human Pluripotent Stem Cell-Derived Multipotent Vascular Progenitors of the Mesothelium Lineage Have Utility in Tissue Engineering and Repair 2019 ·Cell Reports ·(unknown),(unknown),Sebastian Kreß,David M. Reynolds,(unknown),Kristopher L. Nazor,Johannes Baur,Amar M. Singh,Jeanne F. Loring,Marco Metzger,Stephen Dalton	17
4	Myelodysplastic syndrome progression to acute myeloid leukemia at the stem cell level 2018 ·Nature Medicine ·Jiahao Chen,(unknown),Daqian Sun,Tihomira I. Todorova,David M. Reynolds,Swathi-Rao Narayanagari,Cristina Montagna,Britta Will,Amit Verma,Ulrich Steidl	149
5	Whole-Genome Sequencing and iPLEX MassARRAY Genotyping Map an EMS-Induced Mutation Affecting Cell Competition in Drosophila melanogaster 2016 ·G3 Genes Genomes Genetics ·Chang Hyun Lee,(unknown),David M. Reynolds,(unknown),Nicholas E. Baker	26
6	Amnion as a surrogate tissue reporter of the effects of maternal preeclampsia on the fetus 2016 ·Clinical Epigenetics ·Masako Suzuki,Ryo Maekawa,Nicole E. Patterson,David M. Reynolds,(unknown),Sandra E. Reznik,Hye Heo,Francine Einstein,John M. Greally	11
7	Histone H3 Variant Regulates RNA Polymerase II Transcription Termination and Dual Strand Transcription of siRNA Loci in Trypanosoma brucei 2016 ·PLoS Genetics ·David M. Reynolds,Brigitte T. Hofmeister,Laura Cliffe,Magdy Alabady,T. Nicolai Siegel,Robert J. Schmitz,Robert Sabatini	42
8	Signaling Network Crosstalk in Human Pluripotent Cells: A Smad2/3-Regulated Switch that Controls the Balance between Self-Renewal and Differentiation 2012 ·Cell stem cell ·Amar M. Singh,David M. Reynolds,(unknown),Satoshi Ohtsuka,Alexa L. Mattheyses,Yuhua Sun,Laura Menéndez,Michael Kulik,Stephen Dalton	277
9	Identification of a Locus for Autosomal Dominant Polycystic Liver Disease, on Chromosome 19p13.2-13.1 2000 ·The American Journal of Human Genetics ·David M. Reynolds,C.T. Falk,Airong Li,B F King,Patrick S. Kamath,John Huston,Clarence Shub,Diana M. Iglesias,Rodolfo S. Martín,Yves Pirson,Vicente E. Torres,Stefan Somlo	61
10	Forkhead transcription factors, Fkh1p and Fkh2p, collaborate with Mcm1p to control transcription required for M-phase 2000 ·Current Biology ·Raman Kumar,David M. Reynolds,Andrej Shevchenko,Anna Shevchenko,Sherilyn Goldstone,Stephen Dalton	149
11	Aberrant Splicing in the PKD2 Gene as a Cause of Polycystic Kidney Disease 1999 ·Journal of the American Society of Nephrology ·David M. Reynolds,Tomohito Hayashi,Yiqiang Cai,Barbera Veldhuisen,Terry Watnick,Xosé M. Lens,Toshio Mochizuki,Feng Qian,Yoshiko Maeda,Li Li,Ragnheiður Fossdal,Eliécer Coto,Guanqing Wu,Martijn H. Breuning,Gregory G. Germino,Dorien J.M. Peters,Stefan Somlo	72
12	Somatic Inactivation of Pkd2 Results in Polycystic Kidney Disease 1998 ·Cell ·Guanqing Wu,Vivette D. D’Agati,Yiqiang Cai,Glen S. Markowitz,Jong Hoon Park,David M. Reynolds,Yoshiko Maeda,Thanh C. Le,Harry Hou,Raju Kucherlapati,Winfried Edelmann,Stefan Somlo	456
13	Identification ofPKD2L,a HumanPKD2-Related Gene: Tissue-Specific Expression and Mapping to Chromosome 10q25 1998 ·Genomics ·Guanqing Wu,Tomohito Hayashi,(unknown),Mehul Dixit,David M. Reynolds,Li Li,Yoshiko Maeda,Yiqiang Cai,Miguel Coca‐Prados,Stefan Somlo	86
14	A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2) 1997 ·The American Journal of Human Genetics ·Barbera Veldhuisen,Jasper J. Saris,Simone de Haij,Tomohito Hayashi,David M. Reynolds,Toshio Mochizuki,R Elles,Ragnheiður Fossdal,Nadja Bogdanova,Marjan A. van Dijk,Eliécer Coto,David Ravine,Søren Nørby,C. Verellen‐Dumoulin,M.H. Breuning,Stefan Somlo,Dorien J.M. Peters	77
15	Novel stop and frameshifting mutations in the autosomal dominant polycystic kidney disease 2 (PKD2) gene 1997 ·Human Genetics ·(unknown),Tomohito Hayashi,Dolores Tellerı́a,Toshio Mochizuki,David M. Reynolds,R. Alonso,Xosé M. Lens,Felipe Moreno,Peter C. Harris,Stefan Somlo,José L. San Millán	36
16	Molecular Cloning, cDNA Sequence Analysis, and Chromosomal Localization of MousePkd2 1997 ·Genomics ·Guanqing Wu,Toshio Mochizuki,Thanh C. Le,Yiqiang Cai,Tomohito Hayashi,David M. Reynolds,Stefan Somlo	34
17	Characterization of the Exon Structure of the Polycystic Kidney Disease 2 Gene (PKD2) 1997 ·Genomics ·Tomohito Hayashi,Toshio Mochizuki,David M. Reynolds,Guanqing Wu,(unknown),Stefan Somlo	79
18	Meiotic transmission of a hypomethylated repetitive DNA family in tobacco 1995 ·Theoretical and Applied Genetics ·Boris Vyskot,B. Koukalová,Aleš Kovařı́k,(unknown),David M. Reynolds,M. Bezdék	35
19	Evaluation of ELISA and electron microscopy for the detection of coronavirus and rotavirus in bovine faeces 1984 ·Veterinary Record ·David M. Reynolds,D. Chasey,A. C. Scott,J. C. Bridger	30
20	Identification of coronaviruses in exotic species of Bovidae 1984 ·Veterinary Record ·D. Chasey,David M. Reynolds,J. C. Bridger,(unknown),Andrew M. Scott	15

About David M. Reynolds

David M. Reynolds is a scholar working on Genetics, Molecular Biology and Parasitology, having authored 35 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (12 papers), Renal and related cancers (11 papers) and Genetic Syndromes and Imprinting (9 papers). The work is most often cited by research in Genetics (2.1k citations), Molecular Biology (2.7k citations) and Pathology and Forensic Medicine (529 citations). David M. Reynolds has collaborated with scholars based in United States, Germany and Spain. Frequent co-authors include Stefan Somlo, Guanqing Wu, Yiqiang Cai, Tomohito Hayashi, Toshio Mochizuki, Stephen Dalton, Dorien J.M. Peters, Barbera Veldhuisen, Jasper J. Saris and Martijn H. Breuning. Their work appears in journals such as Science, Cell and Nucleic Acids Research.

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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