DavidWStocktonMD

Medical Genetics • Detroit, MI

Clinical Genetics

Professor, Pediatrics, Wayne State University School of Medicine

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Office
3901 Beaubien St
Detroit, MI 48201
Phone+1 313-745-4513

Fax+1 313-993-8685
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Summary

Dr. David Stockton, MD is a board certified medical geneticist in Detroit, Michigan. He is currently licensed to practice medicine in Michigan and Texas. He is affiliated with DMC Children's Hospital of Michigan and DMC Harper University Hospital.

Education & Training

Baylor College of MedicineResidency, Medical Genetics and Genomics, 1995 - 1997
University of Michigan Health SystemResidency, Internal Medicine, 1992 - 1995
University of Michigan Medical SchoolClass of 1992

Certifications & Licensure

MI State Medical License 1995 - 2026
TX State Medical License 1996 - 2007
American Board of Internal Medicine Internal Medicine
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics

Clinical Trials

Open-Label Study of Uridine Triacetate in Pediatric Patients With Hereditary Orotic Aciduria Start of enrollment: 2014 Apr 01
Completed
Phase 3

Publications & Presentations

PubMed

Motor Responses in Pediatric Pompe Disease in the ADVANCE Participant Cohort.
Tina Duong, Priya S Kishnani, Kristina An Haack, Meredith C Foster, James B Gibson, Catherine Wilson, Si Houn Hahn, Richard Hillman, David Kronn, Nancy D Leslie, Loren...> ;Journal of Neuromuscular Diseases. 2022 Jan 1
5 citations
Cardiac responses in paediatric Pompe disease in the ADVANCE patient cohort.
Barry J. Byrne, Steven D. Colan, Priya S. Kishnani, Meredith C. Foster, Susan Sparks, James B. Gibson, Kristina An Haack, David W. Stockton, Loren D.M. Pena, Si Houn H...> ;Cardiology in the Young. 2021 Aug 23
5 citations
Management of COVID-19 infection in organic acidemias.
Shagun Kaur, Stephanie L. Campbell, David W. Stockton> ;American Journal of Medical Genetics. Part A. 2021 Mar 8
3 citations
Biallelic Variants in LAMB1 Causing Hydranencephaly: A Severe Phenotype of a Rare Malformative Encephalopathy.
Kuntal Sen, Shagun Kaur, David W. Stockton, Mary Nyhuis, Jacquelyn Roberson> ;AJP Reports. 2021 Jan 1
17 citations
Respiratory function during enzyme replacement therapy in late-onset Pompe disease: longitudinal course, prognostic factors, and the impact of time from diagnosis to t...
David W. Stockton, Priya S. Kishnani, Ans T. van der Ploeg, Juan C. Llerena, Matthias Boentert, Mark Roberts, Barry J. Byrne, Roberto Araujo, Sonia S. Maruti, Nathan T...> ;Journal of Neurology. 2020 Jun 10
14 citations
Erratum: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice (Human Molecular Genetics (2013) 22 (1026...
Tyler F. Beck, Danielle Veenma, Oleg A. Shchelochkov, Zhiyin Yu, Bum Jun Kim, Hitisha P. Zaveri, Yolande van Bever, Sunju Choi, Hannie Douben, Terry Bertin, Pragna Pat...> ;Human Molecular Genetics. 2020 Apr 15
19 citations
Thrombotic risk in congenital erythrocytosis due to up-regulated hypoxia sensing is not associated with elevated hematocrit
Victor R. Gordeuk, Galina Y. Miasnikova, Adelina I. Sergueeva, Felipe R. Lorenzo, Xu Zhang, Jihyun Song, David W. Stockton, Josef T. Prchal> ;Haematologica. 2020 Mar 1
65 citations
Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1
Magdalena Koczkowska, Tom Callens, Yunjia Chen, Alicia Gomes, Alesha D. Hicks, Angela Sharp, Eric Johns, Kim Armfield Uhas, Linlea Armstrong, Katherine A. Bosanko, Dus...> ;Human Mutation. 2020 Jan 1
Cardiac Murmur in a Boy with Normal Paternal Prenatal Carrier Screening for Pompe Disease.
Allison Jay, Premchand Anne, David W. Stockton> ;Case Reports in Pediatrics. 2019 Dec 12
6 citations
Clinical characteristics and genotypes in the ADVANCE baseline data set, a comprehensive cohort of US children and adolescents with Pompe disease.
Priya S. Kishnani, James B. Gibson, Michael J. Gambello, Richard Hillman, David W. Stockton, David Kronn, Nancy D. Leslie, Loren D.M. Pena, Pranoot Tanpaiboon, John W....> ;Genetics in Medicine. 2019 May 14
5 citations
Can Functional Polymorphisms in VEGF and MMP Predict Intraventricular Hemorrhage in Extremely Preterm Newborns
Pankaj Prasun, Raghav Madan, Subhash Puthuraya, Divya Subramanian, Ishita Datta, Vaneet Kumar Kalra, Ronald Thomas, David W. Stockton, Senthil K. Sundaram, Joseph H. C...> ;Developmental Neuroscience. 2018 Jan 1
19 citations
Efficacy, safety profile, and immunogenicity of alglucosidase alfa produced at the 4,000-liter scale in US children and adolescents with Pompe disease: ADVANCE, a phas...
Si Houn Hahn, David Kronn, Nancy D. Leslie, Loren D.M. Pena, Pranoot Tanpaiboon, Michael J. Gambello, James B. Gibson, Richard Hillman, David W. Stockton, John W. Day,...> ;Genetics in Medicine. 2018 Mar 22
113 citations
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848
Magdalena Koczkowska, Yunjia Chen, Tom Callens, Alicia Gomes, Angela Sharp, Sherrell Johnson, Meng-Chang Hsiao, Zhenbin Chen, Meena Balasubramanian, Christopher P. Bar...> ;American Journal of Human Genetics. 2018 Jan 4
49 citations
Mucopolysaccharidosis Type I Newborn Screening: Best Practices for Diagnosis and Management
Lorne A. Clarke, Andrea M. Atherton, Barbara K. Burton, Debra L. Day-Salvatore, Paige Kaplan, Nancy D. Leslie, C. Ronald Scott, David W. Stockton, Janet A. Thomas, Jos...> ;The Journal of Pediatrics. 2017 Mar 1
20 citations
Durable and sustained immune tolerance to ERT in Pompe disease with entrenched immune responses
Zoheb B. Kazi, Sean N. Prater, Joyce A. Kobori, David Viskochil, Carrie Bailey, Renuka Gera, David W. Stockton, Paul McIntosh, Amy S. Rosenberg, Priya S. Kishnani> ;JCI Insight. 2016 Jul 21
4 citations
Premature Pubarche in Children with Pompe Disease
Queenie K.-G. Tan, David W. Stockton, Eniko K. Pivnick, Asim F. Choudhri, Stacy Hines-Dowell, Loren D.M. Pena, Melissa A. Deimling, Michael Freemark, Priya S. Kishnani> ;The Journal of Pediatrics. 2015 Apr 1
Methylmalonic acidemia presenting as persistent pulmonary hypertension of the newborn.
Agarwal, R.,Feldman, G. L.,Poulik, J.,Stockton, D. W.,Sood, B. G.> ;J Neonatal Perinatal Med. 2014 Oct 18
4 citations
Survival and developmental milestones among Pompe registry patients with classic infantile-onset Pompe disease with different timing of initiation of treatment with en...
Yin-Hsiu Chien, Ans T. van der Ploeg, Simon Jones, Barry J. Byrne, Ashok Vellodi, Nancy D. Leslie, Eugen Mengel, Suma P. Shankar, Pranoot Tanpaiboon, David W. Stockton...> ;Journal of Neuromuscular Diseases. 2014 Feb 1
11 citations
Novel Frem1-Related Mouse Phenotypes and Evidence of Genetic Interactions with Gata4 and Slit3
Tyler F. Beck, Oleg A. Shchelochkov, Zhiyin Yu, Bum Jun Kim, Andres Hernandez-Garcia, Hitisha P. Zaveri, Colin E. Bishop, Paul A. Overbeek, David W. Stockton, Monica J...> ;Plos One. 2013 Mar 11
26 citations
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.
Tyler F Beck, Danielle Veenma, Oleg A Shchelochkov, Zhiyin Yu, Bum Jun Kim, Hitisha P Zaveri, Yolande van Bever, Sunju Choi, Hannie Douben, Terry K Bertin, Pragna I Pa...> ;Human Molecular Genetics. 2013 Mar 1
33 citations
An Allelic Series of Mice Reveals a Role for RERE in the Development of Multiple Organs Affected in Chromosome 1p36 Deletions
Bum Jun Kim, Hitisha P. Zaveri, Oleg A. Shchelochkov, Zhiyin Yu, Andres Hernandez-Garcia, Michelle L. Seymour, John S. Oghalai, Fred A. Pereira, David W. Stockton, Mon...> ;Plos One. 2013 Feb 25
396 citations
Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants
Santhosh Girirajan, Jill A. Rosenfeld, Bradley P. Coe, Sumit Parikh, Neil R. Friedman, Amy Goldstein, Robyn A. Filipink, Juliann Mcconnell, Brad Angle, Wendy S. Meschi...> ;The New England Journal of Medicine. 2012 Oct 3
96 citations
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database.
Matthew Bower, Rémi Salomon, Judith Allanson, Corinne Antignac, Francesco Benedicenti, Elisa Benetti, Gil Binenbaum, Uffe Birk Jensen, Pierre Cochat, Stéphane Decramer...> ;Human Mutation. 2012 Mar 1
35 citations
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.
Eric Muller, Swaroop Aradhya, Joan F. Atkin, Erin P. Carmany, Alison M. Elliott, Albert E. Chudley, Robin D. Clark, David B. Everman, Shannon Garner, Bryan D. Hall, Ga...> ;American Journal of Medical Genetics. Part A. 2012 Feb 1
5 citations
Unusual physical features and heat stroke presentation for hypohydrotic ectodermal dysplasia.
Pankaj Prasun, Swati A. Karmarkar, Ajay Agarwal, David W. Stockton> ;Clinical Dysmorphology. 2012 Jan 1
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Hospital Affiliations

DMC Harper University HospitalDetroit, Michigan
DMC Children's Hospital of MichiganDetroit, Michigan