Paul J. Benke

5.4k total citations · 1 hit paper
54 papers, 3.0k citations indexed

About

Paul J. Benke is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Paul J. Benke has authored 54 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 16 papers in Genetics and 13 papers in Clinical Biochemistry. Recurrent topics in Paul J. Benke's work include Metabolism and Genetic Disorders (13 papers), Biochemical and Molecular Research (9 papers) and Genomic variations and chromosomal abnormalities (6 papers). Paul J. Benke is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Biochemical and Molecular Research (9 papers) and Genomic variations and chromosomal abnormalities (6 papers). Paul J. Benke collaborates with scholars based in United States, Netherlands and Italy. Paul J. Benke's co-authors include Richard M. Hoar, Paul M. Fernhoff, Narsingh D. Agnish, Ira T. Lott, Cynthia J. Curry, Edward J. Lammer, Georges Stepien, Abdelaziz Heddi, Douglas C. Wallace and Richard I. Kelley and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Paul J. Benke

53 papers receiving 2.9k 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.

Retinoic Acid Embryopathy

1985 1.4k citations Paul J. Benke et al. profile →

Peers

Countries citing papers authored by Paul J. Benke

Since Specialization

Citations

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

Fields of papers citing papers by Paul J. Benke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul J. Benke. 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 Paul J. Benke. The network helps show where Paul J. Benke may publish in the future.

Co-authorship network of co-authors of Paul J. Benke

This figure shows the co-authorship network connecting the top 25 collaborators of Paul J. Benke. A scholar is included among the top collaborators of Paul J. Benke 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 Paul J. Benke. Paul J. Benke 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	Exploiting O-GlcNAc dyshomeostasis to screen O-GlcNAc transferase intellectual disability variants 2024 ·Stem Cell Reports ·(unknown), (unknown), Andrew T. Ferenbach, Maria Teresa Bonati, (unknown), Paul J. Benke, Queenie K.‐G. Tan, Daan M. F. van Aalten	1
2	De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities 2023 ·American Journal of Medical Genetics Part A ·Scott Ward, (unknown), (unknown), Paul J. Benke, Lisa Emrick, Kristen Fisher, (unknown), Hongzheng Dai, (unknown), María J. Guillen Sacoto, (unknown), (unknown), David R. Murdock, Luis Rohena, Karin E. M. Diderich, Hennie T. Brüggenwirth, Brendan Lee, Carlos A. Bacino, Lindsay C. Burrage, Jill A. Rosenfeld	0
3	Analyses of oligodontia phenotypes and genetic etiologies 2021 ·International Journal of Oral Science ·(unknown), Hong Zhang, (unknown), Figen Seymen, Mine Koruyucu, Yelda Kasımoğlu, Jung‐Wook Kim, Hera Kim‐Berman, (unknown), Paul J. Benke, Yiqun Wu, (unknown), Yaqin Zhu, James P. Simmer, Jan C.‐C. Hu	26
4	Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies 2018 ·Molecular Cytogenetics ·Meng Su, Paul J. Benke, Güney Bademci, Filiz Başak Cengiz, Xiaomei Ouyang, (unknown), (unknown), Mustafa Tekin, Yao‐Shan Fan	2
5	Mutations in SLC38A8 and FOXD1 in patients with nystagmus and foveal hypoplasia. 2017 ·Investigative Ophthalmology & Visual Science ·Emma Lord, James A. Poulter, Andrew R. Webster, Panagiotis I. Sergouniotis, Kamron N. Khan, Paul J. Benke, Lee S. Friedman, Manir Ali, Chris F. Inglehearn, Carmel Toomes	1
6	Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth 2017 ·Pediatric Neurology ·Paul J. Benke, Michael Duchowny, Dianalee McKnight	10
7	Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome–Like Phenotype 2010 ·PLoS ONE ·Stephen C. Collins, (unknown), Paul J. Benke, Elizabeth Berry‐Kravis, Fiona J. Gilbert, Ben A. Oostra, Dicky Halley, Michael E. Zwick, David J. Cutler, Stephen T. Warren	23
8	NaV1.7 Gain-of-function Mutations As A Continuum: A1632E Displays Physiological Changes Associated With Erythromelalgia And Paroxysmal Extreme Pain Disorder Mutations And Produces Symptoms Of Both Disorders 2009 ·Biophysical Journal ·Mark Estación, Sulayman D. Dib‐Hajj, Paul J. Benke, René H. M. te Morsche, Emmanuella M. Eastman, Lawrence J. Macala, Joost P.H. Drenth, Stephen G. Waxman	50
9	Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization 2007 ·Human Mutation ·Yao‐Shan Fan, Parul Jayakar, Hongbo Zhu, Deborah Barbouth, Stephanie Sacharow, Ana Morales, Virginia Carver, Paul J. Benke, Peter Mundy, Louis J. Elsas	93
10	Whole blood RNA offers a rapid, comprehensive approach to genetic diagnosis of cardiovascular diseases 2007 ·Genetics in Medicine ·Todd Miller, Lijing You, Robert J. Myerburg, Paul J. Benke, Nanette H. Bishopric	21
11	46,XX sex reversal with partial duplication of chromosome arm 22q 2004 ·American Journal of Medical Genetics Part A ·Tossaporn Seeherunvong, Erasmo M. Perera, Yong Bao, Paul J. Benke, (unknown), Roger P. Donahue, Gary D. Berkovitz	57
12	Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse 2003 ·Nature Genetics ·Jamee M. Bomar, Paul J. Benke, Eric L. Slattery, Radhika Puttagunta, Larry P. Taylor, Eunju Seong, Arne Nystuen, Weidong Chen, Roger L. Albin, Paresh D. Patel, Rick A. Kittles, Val C. Sheffield, Margit Burmeister	109
13	Coordinate Induction of Energy Gene Expression in Tissues of Mitochondrial Disease Patients 1999 ·Journal of Biological Chemistry ·Abdelaziz Heddi, Georges Stepien, Paul J. Benke, Douglas C. Wallace	143
14	Increased oxidative metabolism in phytohemagglutinin-stimulated lymphocytes from patients with systemic lupus erythematosus is associated with serum SSA antibody 1991 ·Biochemical Medicine and Metabolic Biology ·Paul J. Benke, (unknown), (unknown)	8
15	Phytohemagglutinin-stimulated lymphocytes from patients with systemic lupus erythematosus demonstrate DNA damage 1991 ·Metabolism ·Paul J. Benke, (unknown)	6
16	Chemiluminescence is increased in a subgroup of PHA-stimulated lymphocytes from patients with systemic lupus erythematosus and inhibited by 5-lipoxygenase inhibitors 1991 ·Biochemical Medicine and Metabolic Biology ·Paul J. Benke, (unknown), (unknown)	1
17	Scavengers of free radical oxygen affect the generation of low molecular weight DNA in stimulated lymphocytes from patients with systemic lupus erythematosus 1990 ·Metabolism ·Paul J. Benke, (unknown), J Paupe, Elaine Tozman	14
18	Segregation of lymphocyte low-molecular-weight DNA and antinuclear-antibodies in a family with systemic lupus erythematosus in first cousins 1988 ·Human Genetics ·(unknown), Mary A Fletcher, (unknown), (unknown), Roy D. Altman, Paul J. Benke	2
19	Purine Dysfunction in Cells from Patients with Adenosine Deaminase Deficiency 1976 ·Pediatric Research ·Paul J. Benke, (unknown)	1
20	Purine Dysfunction in Cells from Patients with Adenosine Deaminase Deficiency 1976 ·Pediatric Research ·Paul J. Benke, (unknown)	27

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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