David B. Everman

4.2k citations

39 papers · 1.1k indexed · h-index 20

Impact in

Developmental Biology top 2%
- Congenital limb and hand anomalies
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in

Developmental Biology 6
- Congenital limb and hand anomalies 6
Genetics 26
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 3
- Genetic and rare skin diseases. 3

Co-authors: Fiorella Gurrieri Charles E. Schwartz Ramon Y. Birnbaum Nadav Ahituv Julie R. Jones Steven A. Skinner Nathaniel H. Robin Takayuki Yamanaka
Journals: Human Molecular Genetics (3 papers)Journal of Cell Science (2 papers)Biological Psychiatry (1 paper)The Journal of Pediatrics (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: United States Canada Italy

In The Last Decade

David B. Everman

38 papers receiving 1.0k citations

Peers

Countries citing papers authored by David B. Everman

Since Specialization

Citations

This map shows the geographic impact of David B. Everman'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. Everman 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. Everman more than expected).

Fields of papers citing papers by David B. Everman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside David B. Everman, 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 B. Everman Line = papers co-authored together David B. Everman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations Cytogenetic and Genome Research ·Xiaolan Fang, Benjamin Hilton, Katie Clarkson, R. Curtis Rogers, Richard J. Schroer, Anna K. Childers, 符淑霞, Jessica Davis, David B. Everman, Barbara R. DuPont	2023	0
2	Structural model of human PORCN illuminates disease-associated variants and drug-binding sites Journal of Cell Science ·Jia Yu, Carlos Guilherme Murr, Weijun Xu, Julie R. Jones, David B. Everman, Heather Flanagan‐Steet, Thomas H. Keller, David M. Virshup	2021	21
3	MEF2C Hypofunction in Neuronal and Neuroimmune Populations Produces MEF2C Haploinsufficiency Syndrome–like Behaviors in Mice Biological Psychiatry ·Adam J. Harrington, 三郎堀山, Stefano Berto, عبد الله سلیمان, Edgar Changoluisa, Ahlem Assali, Benjamin M. Siemsen, Domingos Pedro, Tsvetkov Ea, И. А. Чупова, Geneviève Konopka, David B. Everman, Michael D. Scofield, Steven A. Skinner, Christopher W. Cowan	2020	36
4	RIT1 oncoproteins escape LZTR1-mediated proteolysis Science ·Pau Castel, Alice Cheng, Antonio Cuevas-Navarro, David B. Everman, Alex G. Papageorge, Dhirendra K. Simanshu, Alexandra T. Tankka, Jacqueline Galeas, Anatoly Urisman, Frank McCormick	2019	57
5	Neurobiologically-based treatments in Rett syndrome: opportunities and challenges Expert Opinion on Orphan Drugs ·Walter E. Kaufmann, Joo P, David B. Everman, Steven A. Skinner	2016	33
6	Clinical, genetic, and molecular aspects of split‐hand/foot malformation: An update American Journal of Medical Genetics Part A ·Fiorella Gurrieri, David B. Everman	2013	36
7	Functional characterization of tissue-specific enhancers in the DLX5/6 locus Human Molecular Genetics ·Ramon Y. Birnbaum, David B. Everman, Karl K. Murphy, Fiorella Gurrieri, Charles E. Schwartz, Nadav Ahituv	2012	45
8	Coding exons function as tissue-specific enhancers of nearby genes Genome Research ·Ramon Y. Birnbaum, E. Josephine Clowney, Toribio Romero, Mee J. Kim, Jingjing Zhao, Takayuki Yamanaka, Magda Mildreth Rodríguez Castilla, Shoa L. Clarke, Aaron M. Wenger, Loan Nguyen, Fiorella Gurrieri, David B. Everman, Charles E. Schwartz, Ohad S. Birk, Gill Bejerano, Stavros Lomvardas, Nadav Ahituv	2012	166
9	Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele Journal of Medical Genetics ·Uppala Radhakrishna, Swapan K. Nath, Ken McElreavey, Uppala Ratnamala, Celi Sun, Amit K. Maiti, Maryline Gagnebin, Frédérique Béna, Etsuzu Shima, Andrew J. Sharp, David B. Everman, Jeffrey C. Murray, Charles E. Schwartz, Stylianos E. Antonarakis, Merlin G. Butler	2012	9
10	A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation Human Genetics ·Christian Babbs, Raoul Heller, David B. Everman, M. Crocker, Stephen R.F. Twigg, Charles E. Schwartz, Henk Giele, Andrew O.M. Wilkie	2007	19
11	Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non‐syndromic split‐hand/foot malformation American Journal of Medical Genetics Part A ·David B. Everman, Jong-Hyun Yun, Robert Lyle, Qu Peng, Michael J. Bamshad, Katie Clarkson, H. Tertsch, Fiorella Gurrieri, A. Micheil Innes, Jacquelyn Roberson, Connie Schrander‐Stumpel, Hans van Bokhoven, Stylianos E. Antonarakis, Charles E. Schwartz	2006	17
12	Split‐hand/split‐foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region American Journal of Medical Genetics Part A ·Robert Lyle, Uppala Radhakrishna, Jean‐Louis Blouin, Sarantis Gagos, David B. Everman, Corinne Gehrig, C.D. DeLozier-Blanchet, J. V. Solanki, Jennie Mao, Swapan K. Nath, Fiorella Gurrieri, Giovanni Neri, Charles E. Schwartz, Stylianos E. Antonarakis	2006	27
13	Autosomal dominant inheritance of infantile myofibromatosis American Journal of Medical Genetics Part A ·Dina J. Zand, Dale S. Huff, David B. Everman, Karen Russell, Sulagna C. Saitta, Donna M. McDonald‐McGinn, Elaine H. Zackai	2004	37
14	The FU gene and its possible protein isoforms BMC Genomics ·Torben Østerlund, David B. Everman, Regina C. Betz, Monica Mosca, Markus M. Nöthen, Charles E. Schwartz, Peter G. Zaphiropoulos, Rune Toftgård	2004	13
15	Respiratory failure requiring extracorporeal membrane oxygenation after sodium phosphate enema intoxication European Journal of Pediatrics ·David B. Everman, Mara Nitu, Brian R. Jacobs	2003	11
16	Broad phenotypic spectrum caused by an identical heterozygous CDMP‐1 mutation in three unrelated families American Journal of Medical Genetics Part A ·Ravi Savarirayan, Susan M. White, Frances R. Goodman, John M. Graham, Martin B. Delatycki, Ralph S. Lachman, David L. Rimoin, David B. Everman, Matthew L. Warman	2002	45
17	The mutational spectrum of brachydactyly type C American Journal of Medical Genetics ·David B. Everman, Cynthia F. Bartels, Yue Yang, Niranjan Yanamandra, Frances R. Goodman, Roberto Mendoza‐Londono, Ravi Savarirayan, Susan M. White, John M. Graham, Robert Peter Gale, Eva Svarch, William G. Newman, Percival Motha, Clair A. Francomano, Govindaiah Vinukonda, Lalji Singh, Stuart Morrison, J. Terrig Thomas, Matthew L. Warman	2002	65
18	Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules Journal of the American Academy of Child & Adolescent Psychiatry ·David B. Everman, Suzanne B. Cassidy	2000	7
19	Serum α-fetoprotein levels in Beckwith-Wiedemann syndrome The Journal of Pediatrics ·David B. Everman, Cheryl Shuman, Archie Parnell, Mary Ann O’Riordan, Rosanna Weksberg, Nathaniel H. Robin	2000	54
20	Detection of free radicals during the cellular metabolism of adriamycin Free Radical Biology and Medicine ·Rania Taguelmane, David B. Everman, Fransiska Riska, Charles Fields	1990	15

About David B. Everman

David B. Everman is a scholar working on Developmental Biology, Genetics, Biophysics, Immunology and Allergy and Molecular Biology, having authored 39 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Congenital limb and hand anomalies (6 papers), Prenatal Screening and Diagnostics (6 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Hedgehog Signaling Pathway Studies (4 papers), Genetic Syndromes and Imprinting (3 papers) and Genetic and rare skin diseases. (3 papers). The work is most often cited by research in Developmental Biology (134 citations), Genetics (466 citations), Molecular Biology (657 citations), Pediatrics, Perinatology and Child Health (146 citations) and Developmental Neuroscience (22 citations). David B. Everman has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Fiorella Gurrieri, Charles E. Schwartz, Ramon Y. Birnbaum, Nadav Ahituv, Julie R. Jones, Steven A. Skinner, Nathaniel H. Robin, Takayuki Yamanaka, Gill Bejerano and Charles Fields. Their work appears in journals such as Human Molecular Genetics, Journal of Cell Science, Biological Psychiatry, The Journal of Pediatrics and European Journal of Human 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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