David W. Stockton

8.1k citations

70 papers · 4.9k indexed · 1 hit paper · h-index 32

Molecular Biology top 2%
Genetics top 1%
Cellular and Molecular Neuroscience top 1%
Cancer Research top 5%
Neurology top 2%

Co-authors: Huda Y. Zoghbi Tetsuo Ashizawa Chris Amos William B. Dobyns Jennifer M. Bailey Olga Zhuchenko Penelope E. Bonnen Cheng Chi Lee
Topics: Lysosomal Storage Disorders Research (11 papers)Glycogen Storage Diseases and Myoclonus (7 papers)Cancer, Hypoxia, and Metabolism (6 papers)
Cited by: Cellular and Molecular Neuroscience Oral Surgery Molecular Biology
Journals: Nature Nature Genetics Blood
Partner nations: United States United Kingdom Netherlands

In The Last Decade

David W. Stockton

69 papers receiving 4.7k 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.

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel

1997 1.2k citations David W. Stockton, Huda Y. Zoghbi et al. Nature Genetics profile →

Peers

Countries citing papers authored by David W. Stockton

Since Specialization

Citations

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

Fields of papers citing papers by David W. Stockton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David W. Stockton

This figure shows the co-authorship network connecting the top 25 collaborators of David W. Stockton. A scholar is included among the top collaborators of David W. Stockton 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 W. Stockton. David W. Stockton 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	Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort 2022 ·Journal of Neuromuscular Diseases ·Tina Duong,Priya S. Kishnani,Kristina An Haack,Meredith C. Foster,James B. Gibson,Catherine Wilson,Si Houn Hahn,Richard E. Hillman,David Kronn,Nancy D. Leslie,Loren Peña,Susan Sparks,David W. Stockton,Pranoot Tanpaiboon,John Day	3
2	Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy 2021 ·American Journal of Perinatology Reports ·(unknown),(unknown),David W. Stockton,(unknown),Jacquelyn Roberson	4
3	Clinical characteristics and genotypes in the ADVANCE baseline data set, a comprehensive cohort of US children and adolescents with Pompe disease 2019 ·Genetics in Medicine ·Priya S. Kishnani,James B. Gibson,Michael J. Gambello,Richard E. Hillman,David W. Stockton,David Kronn,Nancy D. Leslie,Loren Peña,Pranoot Tanpaiboon,John Day,Raymond Wang,Jennifer Goldstein,Kristina An Haack,Susan Sparks,Yang Zhao,Si Houn Hahn	9
4	Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis 2010 ·Human Genetics ·Wojciech Wiszniewski,Richard A. Lewis,David W. Stockton,(unknown),Graeme Mardon,Rui Chen,James R. Lupski	19
5	Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity 2010 ·Genetics in Medicine ·Ruxandra Bachmann‐Gagescu,Heather C. Mefford,Charles A. Cowan,Gwen M. Glew,Anne Hing,Stephanie E Wallace,Patricia I. Bader,(unknown),Pamela J. Reitnauer,Rosemarie Smith,David W. Stockton,Hiltrud Muhle,Ingo Helbig,Evan E. Eichler,Blake C. Ballif,Jill A. Rosenfeld,Karen D. Tsuchiya	137
6	Isolation and characterization of mouse–human microcell hybrid cell clones permissive for infectious HIV particle release 2007 ·Virology ·(unknown),(unknown),(unknown),David W. Stockton,(unknown),Svetlana A. Yatsenko,Richard E. Sutton	6
7	Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 2006 ·Human Genetics ·Erica R. Eichers,Muhammad M. Abd‐El‐Barr,Richard Paylor,Richard A. Lewis,Weimin Bi,Xiaodi Lin,Thomas P. Meehan,David W. Stockton,Samuel M. Wu,Elizabeth Lindsay,Monica J. Justice,Philip L. Beales,Nicholas Katsanis,James R. Lupski	87
8	Congenital polycythemias/erythrocytoses. 2005 ·PubMed ·Victor R. Gordeuk,David W. Stockton,Josef T. Prchal	72
9	Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS 2005 ·The American Journal of Human Genetics ·Roberto Mendoza‐Londono,Edward J. Lammer,Rosemarie Watson,John Harper,Atsushi Hatamochi,(unknown),Dobrawa Napierala,Pia Hermanns,(unknown),Benjamin B. Roa,(unknown),Keiko Wakui,Diep Nguyen,David W. Stockton,Brendan Lee	13
10	Search for genetic determinants of individual variability of the erythropoietin response to high altitude 2003 ·Blood Cells Molecules and Diseases ·Katerina Jedlickova,David W. Stockton,Hua Chen,James Stray‐Gundersen,Sarah Witkowski,Ri‐Li Ge,Jaroslav Jelı́nek,Benjamin D. Levine,Josef T. Prchal	33
11	Newfoundland Rod-Cone Dystrophy, an Early-Onset Retinal Dystrophy, Is Caused by Splice-Junction Mutations in RLBP1 2002 ·The American Journal of Human Genetics ·Erica R. Eichers,Jane S. Green,David W. Stockton,(unknown),(unknown),J. Arch McNamara,(unknown),James R. Lupski,Nicholas Katsanis	70
12	Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia 2002 ·Human Genetics ·Parimal Das,David W. Stockton,(unknown),Lisa G. Shaffer,Rena N. D’Souza,Timothy J. Wright,Pragna I. Patel	121
13	Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia 2002 ·Nature Genetics ·Sonny Ang,Hua Chen,Kiichi Hirota,Victor R. Gordeuk,Jaroslav Jelı́nek,Yongli Guan,Enli Liu,Adelina Sergueeva,Galina Miasnikova,David R. Mole,Patrick H. Maxwell,David W. Stockton,Gregg L. Semenza,Josef T. Prchal	382
14	Endemic Polycythemia in Russia: Mutation in the VHL Gene 2002 ·Blood Cells Molecules and Diseases ·Sonny Ang,Chen Hua,Victor R. Gordeuk,Adelina Sergueeva,Lydia A. Polyakova,Galina Miasnikova,Róbert Královics,David W. Stockton,Josef T. Prchal	105
15	Hereditary Neuropathy With Liability to Pressure Palsies Is Not a Major Cause of Idiopathic Carpal Tunnel Syndrome 2001 ·Archives of Neurology ·David W. Stockton,Ricardo A. Meade,David T. Netscher,Michael Epstein,Saleh M. Shenaq,Lisa G. Shaffer,James R. Lupski	12
16	Terminal Osseous Dysplasia with Pigmentary Defects Maps to Human Chromosome Xq27.3-Xqter 2000 ·The American Journal of Human Genetics ·Wenzheng Zhang,(unknown),David W. Stockton,Ignatia B. Van den Veyver,(unknown),Huda Y. Zoghbi	17
17	Terminal osseous dysplasia and pigmentary defects: Clinical characterization of a novel male lethal X-linked syndrome 2000 ·American Journal of Medical Genetics ·Carlos A. Bacino,David W. Stockton,(unknown),Heidi A. Heilstedt,Raymond Lewandowski,Ignatia B. Van den Veyver	21
18	Delineation of the Critical Interval of Bardet-Biedl Syndrome 1 (BBS1) to a Small Region of 11q13, through Linkage and Haplotype Analysis of 91 Pedigrees 1999 ·The American Journal of Human Genetics ·Nicholas Katsanis,Richard A. Lewis,David W. Stockton,(unknown),Lisa Baird,Philip L. Beales,Mark Leppert,James R. Lupski	39
19	A novel locus for Leber congenital amaurosis on chromosome 14q24 1998 ·Human Genetics ·David W. Stockton,Richard A. Lewis,Emad B. Abboud,Ali A. Al‐Rajhi,Monzer Jabak,Kent L. Anderson,James R. Lupski	62
20	Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: A brief review 1997 ·American Journal of Medical Genetics ·David W. Stockton,(unknown),(unknown),(unknown),Lisa G. Shaffer,(unknown)	12

About David W. Stockton

David W. Stockton is a scholar working on Genetics, Rheumatology and Genetics, having authored 70 papers that have together received 4.9k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (11 papers), Glycogen Storage Diseases and Myoclonus (7 papers) and Cancer, Hypoxia, and Metabolism (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.3k citations), Oral Surgery (483 citations) and Molecular Biology (3.3k citations). David W. Stockton has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Huda Y. Zoghbi, Tetsuo Ashizawa, Chris Amos, William B. Dobyns, Jennifer M. Bailey, Olga Zhuchenko, Penelope E. Bonnen, Cheng Chi Lee, S. H. Subramony and Pragna I. Patel. Their work appears in journals such as Nature, Nature Genetics and Blood.

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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