David R. Murdock

2.6k total citations
35 papers, 659 citations indexed

About

David R. Murdock is a scholar working on Genetics, Molecular Biology and Biomedical Engineering. According to data from OpenAlex, David R. Murdock has authored 35 papers receiving a total of 659 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Biomedical Engineering. Recurrent topics in David R. Murdock's work include Genomics and Rare Diseases (18 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetics and Neurodevelopmental Disorders (8 papers). David R. Murdock is often cited by papers focused on Genomics and Rare Diseases (18 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetics and Neurodevelopmental Disorders (8 papers). David R. Murdock collaborates with scholars based in United States, Canada and United Kingdom. David R. Murdock's co-authors include Richard A. Gibbs, Bahman Anvari, William E. Brownell, Sergey A. Ermilov, Donna M. Muzny, Irene Newsham, Matthew N. Bainbridge, James R. Lupski, Jennifer Friedman and Marie‐Claude Gingras and has published in prestigious journals such as Journal of Clinical Investigation, Journal of the American College of Cardiology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

David R. Murdock

31 papers receiving 646 citations

Peers

Countries citing papers authored by David R. Murdock

Since Specialization

Citations

This map shows the geographic impact of David R. Murdock'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. Murdock 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. Murdock more than expected).

Fields of papers citing papers by David R. Murdock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David R. Murdock

This figure shows the co-authorship network connecting the top 25 collaborators of David R. Murdock. A scholar is included among the top collaborators of David R. Murdock 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 R. Murdock. David R. Murdock 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	Early diagnosis of vascular Ehlers-Danlos syndrome through AI-powered facial analysis: Results from the Montalcino Aortic Consortium 2025 ·Genetics in Medicine Open ·David R. Murdock, (unknown), Ernesto Calderón Martinez, (unknown), (unknown), Alan C. Braverman, Anji T. Yetman, Shaine A. Morris, Dianna M. Milewicz	0
2	MYH11 rare variant augments aortic growth and induces cardiac hypertrophy and heart failure with pressure overload 2025 ·PLoS Genetics ·Zhen Zhou, (unknown), (unknown), (unknown), Michael P. Massett, Mingjie Zheng, Alana C. Cecchi, Dongchuan Guo, David R. Murdock, (unknown), (unknown), Jun Wang, John M. Greally, Dianna M. Milewicz	0
3	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
4	An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation family 2023 ·Clinical Genetics ·Dongchuan Guo, Xueyan Duan, (unknown), Alana C. Cecchi, (unknown), Yang Yu, (unknown), Kwanghyuk Lee, (unknown), David R. Murdock, Suzanne M. Leal, Marsha M. Wheeler, Josh Smith, Michael J. Bamshad, Dianna M. Milewicz	2
5	PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature 2022 ·American Journal of Medical Genetics Part A ·(unknown), David R. Murdock, Lindsay C. Burrage, Hongzheng Dai, Seema R. Lalani, Richard A. Lewis, (unknown), (unknown), Jill A. Rosenfeld, Alyssa A. Tran, James B. Gibson, (unknown), Carlos A. Bacino, Brendan Lee, Hsiao‐Tuan Chao	2
6	Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study 2022 ·Circulation Genomic and Precision Medicine ·Hadley Stevens Smith, (unknown), (unknown), (unknown), David R. Murdock, Ginger Metcalf, (unknown), (unknown), Eric Boerwinkle, Xander H.T. Wehrens, Christie M. Ballantyne, Richard A. Gibbs, Amy L. McGuire, Stacey Pereira	0
7	A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay 2022 ·Human Mutation ·Hongzheng Dai, Wenmiao Zhu, Bo Yuan, Sophie Nicole, Kelly Schoch, Yong‐hui Jiang, John A. Phillips, Melissa S. Jones, Pengfei Liu, David R. Murdock, Lindsay C. Burrage, Brendan Lee, Jill A. Rosenfeld, Rui Xiao, (unknown)	3
8	Exome sequencing in children with clinically suspected maturity‐onset diabetes of the young 2021 ·Pediatric Diabetes ·Mustafa Tosur, Claudia Soler‐Alfonso, (unknown), Michael M. Khayat, Shalini N. Jhangiani, Qingchang Meng, (unknown), Donna M. Muzny, Richard A. Gibbs, David R. Murdock, Jennifer E. Posey, Ashok Balasubramanyam, María J. Redondo, Aniko Sabo	5
9	A novel de novo intronic variant in ITPR1 causes Gillespie syndrome 2021 ·American Journal of Medical Genetics Part A ·(unknown), Ming‐Ming Jiang, Xiaohui Li, Ronit Marom, Hongzheng Dai, David R. Murdock, Pengfei Liu, Jill V. Hunter, Jason D. Heaney, Laurie Robak, Lisa Emrick, Timothy Lotze, Lauren S. Blieden, (unknown), Richard A. Lewis, Alex V. Levin, Jenina Capasso, William J. Craigen, Jill A. Rosenfeld, Brendan Lee, Lindsay C. Burrage	5
10	HEARTCARE: ADVANCING PRECISION MEDICINE THROUGH COMPREHENSIVE CARDIOVASCULAR GENETIC TESTING 2020 ·Journal of the American College of Cardiology ·Ginger Metcalf, David R. Murdock, Eric Venner, Mullai Murugan, Donna M. Muzny, Stacey Pereira, Eric Boerwinkle, Christie M. Ballantyne, Richard A. Gibbs	1
11	De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy 2020 ·The American Journal of Human Genetics ·Hyung-Lok Chung, Xiao Mao, Hua Wang, Ye-Jin Park, Paul C. Marcogliese, Jill A. Rosenfeld, Lindsay C. Burrage, Pengfei Liu, David R. Murdock, Shinya Yamamoto, Michael F. Wangler, Hsiao‐Tuan Chao, (unknown), Li Feng, Carlos A. Bacino, Hugo J. Bellen, Bo Xiao	28
12	Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing 2020 ·Journal of Clinical Investigation ·David R. Murdock, Hongzheng Dai, Lindsay C. Burrage, Jill A. Rosenfeld, Shamika Ketkar, Michaela Müller, Vicente A. Yépez, Julien Gagneur, Pengfei Liu, Shan Chen, Mahim Jain, Gladys Zapata, Carlos A. Bacino, Hsiao‐Tuan Chao, Paolo Moretti, William J. Craigen, Neil A. Hanchard, Brendan Lee	93
13	Enhancing Diagnosis Through RNA Sequencing 2020 ·Clinics in Laboratory Medicine ·David R. Murdock	11
14	Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition 2019 ·Molecular Case Studies ·David R. Murdock, Yunyun Jiang, Michael F. Wangler, Michael M. Khayat, Aniko Sabo, Jane Juusola, Kirsty McWalter, (unknown), Meral Gunay‐Aygun, Richard A. Gibbs	13
15	SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly 2017 ·Congenital Anomalies ·(unknown), Seth Berger, (unknown), Karin Weiss, Ariel F. Martinez, Donald W. Hadley, David R. Murdock, (unknown), Robin D. Clark, Erich Roessler, Paul Kruszka, Maximilian Muenke	10
16	Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/PIGN‐related epilepsy 2015 ·American Journal of Medical Genetics Part A ·Leah Fleming, Monica E. Lemmon, (unknown), (unknown), Weiyi Mu, David R. Murdock, Joann Bodurtha, Julie Hoover‐Fong, Ronald D. Cohn, Thangamadhan Bosemani, Kristin Barañano, Ada Hamosh	34
17	Structural variation and missense mutation in SBDSassociated with Shwachman-Diamond syndrome 2014 ·BMC Medical Genetics ·Claudia M.B. Carvalho, Luciana W. Zuccherato, Christopher L. Williams, Nicholas J. Neill, David R. Murdock, Matthew N. Bainbridge, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, Wan Ip, R. Paul Guillerman, James R. Lupski, Alison A. Bertuch	6
18	Whole‐exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria 2011 ·American Journal of Medical Genetics Part A ·David R. Murdock, Gary Clark, Matthew N. Bainbridge, Irene Newsham, Yuanqing Wu, Donna M. Muzny, Sau Wai Cheung, Richard A. Gibbs, Melissa B. Ramocki	40
19	Studies of plasma membrane mechanics and plasma membrane–cytoskeleton interactions using optical tweezers and fluorescence imaging 2006 ·Journal of Biomechanics ·Sergey A. Ermilov, David R. Murdock, Feng Qian, William E. Brownell, Bahman Anvari	18
20	Effects of Salicylate on Plasma Membrane Mechanics 2005 ·Journal of Neurophysiology ·Sergey A. Ermilov, David R. Murdock, Dania Daye, William E. Brownell, Bahman Anvari	24

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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