David W. Stockton

8.1k citations

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

Cellular and Molecular Neuroscience top 1%
Oral Surgery top 1%
Molecular Biology top 2%
- Hedgehog Signaling Pathway Studies 4
- dental development and anomalies 4
Genetics top 1%
- Genetic Syndromes and Imprinting 4
Genetics top 2%
- Genetic Syndromes and Imprinting 4
Physiology
- Lysosomal Storage Disorders Research 11
Rheumatology
- Glycogen Storage Diseases and Myoclonus 7
Cancer Research
- Cancer, Hypoxia, and Metabolism 6
Pulmonary and Respiratory Medicine
- Neonatal Respiratory Health Research 4
Psychiatry and Mental health
- Child Nutrition and Feeding Issues 3

Co-authors: Huda Y. Zoghbi Tetsuo Ashizawa Chris Amos William B. Dobyns Jennifer M. Bailey Olga Zhuchenko Penelope E. Bonnen Cheng Chi Lee
Cited by: Cellular and Molecular Neuroscience Oral Surgery Molecular Biology
Journals: Nature (1 paper)Nature Genetics (4 papers)Blood (2 papers)
Partner nations: United States United Kingdom Netherlands

In The Last Decade

David W. Stockton

69 papers receiving 4.7k citations

Hit Papers

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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

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

All Works

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20 of 20 papers shown

#	Work
1	Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort 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	2022	3
2	Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy American Journal of Perinatology Reports ·Kuntal Sen,Shagun Kaur,David W. Stockton,Mary Nyhuis,Jacquelyn Roberson	2021	4
3	Clinical characteristics and genotypes in the ADVANCE baseline data set, a comprehensive cohort of US children and adolescents with Pompe disease 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	2019	9
4	Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis Human Genetics ·Wojciech Wiszniewski,Richard A. Lewis,David W. Stockton,Jianlan Peng,Graeme Mardon,Rui Chen,James R. Lupski	2010	19
5	Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity Genetics in Medicine ·Ruxandra Bachmann‐Gagescu,Heather C. Mefford,Charles A. Cowan,Gwen M. Glew,Anne Hing,Stephanie E Wallace,Patricia I. Bader,Aline I. Hamati,Pamela J. Reitnauer,Rosemarie Smith,David W. Stockton,Hiltrud Muhle,Ingo Helbig,Evan E. Eichler,Blake C. Ballif,Jill A. Rosenfeld,Karen D. Tsuchiya	2010	137
6	Isolation and characterization of mouse–human microcell hybrid cell clones permissive for infectious HIV particle release Virology ·Ayse K. Coskun,Marc van Maanen,David Janka,David W. Stockton,Pawel Stankiewicsz,Svetlana A. Yatsenko,Richard E. Sutton	2007	6
7	Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 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	2006	87
8	Congenital polycythemias/erythrocytoses. PubMed ·Victor R. Gordeuk,David W. Stockton,Josef T. Prchal	2005	72
9	Characterization of a New Syndrome That Associates Craniosynostosis, Delayed Fontanel Closure, Parietal Foramina, Imperforate Anus, and Skin Eruption: CDAGS The American Journal of Human Genetics ·Roberto Mendoza‐Londono,Edward J. Lammer,Rosemarie Watson,John Harper,Atsushi Hatamochi,Saori Hatamochi-Hayashi,Dobrawa Napierala,Pia Hermanns,Sinéad Collins,Benjamin B. Roa,Madhuri Hedge,Keiko Wakui,Diep Nguyen,David W. Stockton,Brendan Lee	2005	13
10	Search for genetic determinants of individual variability of the erythropoietin response to high altitude 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	2003	33
11	Newfoundland Rod-Cone Dystrophy, an Early-Onset Retinal Dystrophy, Is Caused by Splice-Junction Mutations in RLBP1 The American Journal of Human Genetics ·Erica R. Eichers,Jane S. Green,David W. Stockton,Christopher S. Jackman,James Whelan,J. Arch McNamara,(unknown),James R. Lupski,Nicholas Katsanis	2002	70
12	Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia Human Genetics ·Parimal Das,David W. Stockton,Christopher C. Bauer,Lisa G. Shaffer,Rena N. D’Souza,Timothy J. Wright,Pragna I. Patel	2002	121
13	Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia 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	2002	382
14	Endemic Polycythemia in Russia: Mutation in the VHL Gene 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	2002	105
15	Hereditary Neuropathy With Liability to Pressure Palsies Is Not a Major Cause of Idiopathic Carpal Tunnel Syndrome Archives of Neurology ·David W. Stockton,Ricardo A. Meade,David T. Netscher,Michael Epstein,Saleh M. Shenaq,Lisa G. Shaffer,James R. Lupski	2001	12
16	Terminal Osseous Dysplasia with Pigmentary Defects Maps to Human Chromosome Xq27.3-Xqter The American Journal of Human Genetics ·Wenzheng Zhang,Ruthie Amir,David W. Stockton,Ignatia B. Van den Veyver,Carlos A. Bacino,Huda Y. Zoghbi	2000	17
17	Terminal osseous dysplasia and pigmentary defects: Clinical characterization of a novel male lethal X-linked syndrome American Journal of Medical Genetics ·Carlos A. Bacino,David W. Stockton,Roberta A. Sierra,Heidi A. Heilstedt,Raymond Lewandowski,Ignatia B. Van den Veyver	2000	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 The American Journal of Human Genetics ·Nicholas Katsanis,Richard A. Lewis,David W. Stockton,Phuong M.T.,Lisa Baird,Philip L. Beales,Mark Leppert,James R. Lupski	1999	39
19	A novel locus for Leber congenital amaurosis on chromosome 14q24 Human Genetics ·David W. Stockton,Richard A. Lewis,Emad B. Abboud,Ali A. Al‐Rajhi,Monzer Jabak,Kent L. Anderson,James R. Lupski	1998	62
20	Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: A brief review American Journal of Medical Genetics ·David W. Stockton,Helen L. Ross,Carlos A. Bacino,Carolyn A. Altman,Lisa G. Shaffer,James R. Lupski	1997	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), Cancer, Hypoxia, and Metabolism (6 papers), Genetic Syndromes and Imprinting (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Neonatal Respiratory Health Research (4 papers), dental development and anomalies (4 papers) and Child Nutrition and Feeding Issues (3 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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