V. Reid Sutton

ScholarGPS® ID: 12417612993158

Affiliation

Baylor College of Medicine, Houston, United States

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Metrics Summary

Publication Count

186

Predicted Citations

7,162

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosis (journal article) Glinton, Kevin E. \| Gijavanekar, Charul \| Rajagopal, Abbhirami \| Mackay, Laura P. \| Martin, Kirt A. \| Pearl, Phillip L. \| Gibson, K. Michael \| Wilson, Theresa A. \| Sutton, V. Reid \| Elsea, Sarah H. Frontiers in Genetics, volume 15 (2024). 10.3389/fgene.2024.1405468 Cite \| Source
Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis Imperfecta (journal article) Cho, Hannah E. \| Shepherd, Whitney S. \| Colombo, Gianna M. \| Wiese, Andrew D. \| Rork, W. Conor \| Kostick, Kristin M. \| Nguyen, Dianne \| Murali, Chaya N. \| Robinson, Marie-Eve \| Schneider, Sophie C. \| ... \| Storch, Eric A. Disability and Rehabilitation (2024). 10.1080/09638288.2024.2358903 Cite \| Source
Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism (journal article) Coody, Troy \| De Biase, Irene \| Sutton, V. Reid \| Pasquali, Marzia \| Shayota, Brian Molecular Genetics and Metabolism, volume 141, issue 4, pages 108215- (2024). 10.1016/j.ymgme.2024.108215 Cite \| Source
Effective algorithm to differentiate NBS MCADD cases from false positives and an assessment of the utility of the second newborn screen for MCADD (journal article) Snyder, Matthew \| Divin, Kristian \| Liu, Ning \| Sun, Qin \| Wang, Yue \| Luo, Xi \| Burrage, Lindsay \| Sutton, V. Reid Molecular Genetics and Metabolism, volume 141, issue 4, pages 108168- (2024). 10.1016/j.ymgme.2024.108168 Cite \| Source
IT translates: An update on the ARCT-810 mRNA therapy for OTC deficiency (journal article) McNutt, Markey \| Vockley, Jerry \| Zori, Roberto \| Basel, Donald \| Breilyn, Margo \| Longo, Nicola \| Sutton, Vernon \| Berry, Susan \| Chivukula, Pad \| Crowley, Constance \| Geller, David Molecular Genetics and Metabolism, volume 141, issue 4, pages 108161- (2024). 10.1016/j.ymgme.2024.108161 Cite \| Source
Cranio‐cervical abnormalities in moderate‐to‐severe osteogenesis imperfecta – Genotypic and phenotypic determinants (journal article) Marulanda, Juliana \| Retrouvey, Jean‐Marc \| Lee, Brendan \| Sutton, V. Reid \| Rauch, Frank \| Briner, Michelle Orthodontics & Craniofacial Research, volume 27, issue 2, pages 237-243 (2024). 10.1111/ocr.12707 Cite \| Source
Velmanase alfa approved for treatment of non-central nervous system manifestations of alpha-mannosidosis: A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG) (journal article) Lander, Julie M. \| Penon-Portmann, Monica \| Sutton, V. Reid \| Chang, Irene Genetics in Medicine Open, volume 2 (2024). 10.1016/j.gimo.2024.101832 Cite \| Source
Elevated amyloid beta peptides and total tau in cerebrospinal fluid in individuals with Creatine transporter deficiency (journal article) Rahhal, Samar \| Farmer, Cristan \| Thurm, Audrey \| Wassif, Christopher A. \| Cawley, Niamh X. \| Perreault, John \| Dang Do, An \| Bianconi, Simona \| Hannah-Shmouni, Fady \| Guthrie, Whitney \| ... \| Porter, Forbes D. Molecular Genetics and Metabolism Reports, volume 37 (2023). 10.1016/j.ymgmr.2023.101001 Cite \| Source
A qualitative exploration of patient perspectives on psychosocial burdens and positive factors in adults with osteogenesis imperfecta (journal article) Rork, W. Conor \| Hertz, Alyssa G. \| Wiese, Andrew D. \| Kostick, Kristin M. \| Nguyen, Dianne \| Schneider, Sophie C. \| Shepherd, Whitney S. \| Cho, Hannah \| Murali, Chaya N. \| Lee, Brendan \| ... \| Storch, Eric A. American Journal of Medical Genetics Part A, volume 191, issue 9, pages 2267-2275 (2023). 10.1002/ajmg.a.63323 Cited by (3) \| Cite \| Source
Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn Screen (journal article) McCann-Crosby, Bonnie \| Liang, Mark C. \| Geffner, Mitchell E. \| Koppin, Christina M. \| Fraga, Nicole R. \| Sutton, V. Reid \| Karaviti, Lefkothea P. \| Bhullar, Gagandeep \| Kim, Mimi S. International Journal of Neonatal Screening, volume 9, issue 3, pages 50- (2023). 10.3390/ijns9030050 Cite \| Source
Approach to the Patient: Pharmacological Therapies for Fracture Risk Reduction in Adults With Osteogenesis Imperfecta (journal article) Liu, Winnie \| Lee, Brendan \| Nagamani, Sandesh C S \| Nicol, Lindsey \| Rauch, Frank \| Rush, Eric T \| Sutton, V Reid \| Orwoll, Eric The Journal of Clinical Endocrinology & Metabolism, volume 108, issue 7, pages 1787-1796 (2023). 10.1210/clinem/dgad035 Cited by (12) \| Cite \| Source
Dual enzyme therapy improves adherence to chemotherapy in a patient with gaucher disease and Ewing sarcoma (journal article) Lucari, Brandon \| Tallis, Eran \| Sutton, Vernon Reid \| Porea, Timothy Pediatric Hematology and Oncology, volume 40, issue 4, pages 422-428 (2023). 10.1080/08880018.2022.2124006 Cited by (1) \| Cite \| Source
Prenatal diagnosis of vascular anomalies (journal article) Agarwal, Shreya \| Mehollin‐Ray, Amy \| Sutton, Vernon R. \| Iacobas, Ionela Prenatal Diagnosis, volume 43, issue 3, pages 318-327 (2023). 10.1002/pd.6321 Cited by (5) \| Cite \| Source
SUCCESSFUL OUTPATIENT TRANSITION TO EXTENDED-RELEASE CORNSTARCH IN PATIENTS WITH GLYCOGEN STORAGE DISEASE (journal article) Snyder, Matthew \| Rawls-Castillo, Brandy \| Aquino, Nathaly \| Al-shwaf, Sarah \| Craigen, William \| Scaglia, Fernando \| Sutton, V. Reid \| Soler-Alfonso, Claudia Molecular Genetics and Metabolism, volume 138, issue 3, pages 107491- (2023). 10.1016/j.ymgme.2023.107491 Cite \| Source
COMPREHENSIVE SCREENING OF BLOOD-BASED BIOMARKERS IMPROVES DIAGNOSIS OF GABA CATABOLISM ABNORMALITIES AND HIGHLIGHTS OPPORTUNITIES TO REDUCE HEALTH DISPARITIES IN GENETIC DIAGNOSIS (journal article) Gijavanekar, Charul \| Glinton, Kevin E. \| Martin, Kirt A. \| Wilson, Theresa A. \| Sutton, Vernon R. \| Elsea, Sarah H. Molecular Genetics and Metabolism, volume 138, issue 3, pages 107415- (2023). 10.1016/j.ymgme.2023.107415 Cite \| Source
P015: Screening for disorders of GABA metabolism: Integration of sequencing and metabolomic screening supports early diagnosis and expands access to care (journal article) Glinton, Kevin \| Gijavanekar, Charul \| Martin, Kirt \| Wilson, Theresa \| Sutton, Vernon \| Elsea, Sarah Genetics in Medicine Open, volume 1, issue 1, pages 100025- (2023). 10.1016/j.gimo.2023.100025 Cite \| Source
Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAP (journal article) Marulanda, Juliana \| Ludwig, Karissa \| Glorieux, Francis \| Lee, Brendan \| Sutton, V. Reid \| Retrouvey, Jean-Marc \| Rauch, Frank Bone, volume 164 (2022). 10.1016/j.bone.2022.116516 Cited by (1) \| Cite \| Source
Obstetrical Challenges in Robinow Syndrome (journal article) Zhang, Yingao \| Casanova, Marco \| Shanahan, Matthew \| Sutton, V. Reid \| Fox, Karin Case Reports in Obstetrics and Gynecology, volume 2022 (2022). 10.1155/2022/6481517 Cite \| Source
A novel, de novo intronic variant in POGZ causes White–Sutton syndrome (journal article) Merriweather, Ashanta \| Murdock, David R. \| Rosenfeld, Jill A. \| Dai, Hongzheng \| Ketkar, Shamika \| Emrick, Lisa \| Nicholas, Sarah \| Lewis, Richard A. \| Bacino, Carlos A. \| Scott, Daryl A. \| ... \| Burrage, Lindsay C. American Journal of Medical Genetics Part A, volume 188, issue 7, pages 2198-2203 (2022). 10.1002/ajmg.a.62747 Cited by (3) \| Cite \| Source
eP235: Interim results of the Vigilan observational study: clinical characteristics of creatine transporter deficiency (journal article) Miller, Judith \| Bianconi, Simona \| Anselm, Irina \| Barshop, Bruce \| Berry-Kravis, Elizabeth \| Cecil, Kim \| Hannah-Shmouni, Fady \| Koeberl, Dwight \| Longo, Nicola \| Mercimek-Andrews, Saadet \| ... \| Thurm, Audrey Genetics in Medicine, volume 24, issue 3, pages S149- (2022). 10.1016/j.gim.2022.01.270 Cite \| Source

Title	Investigators	Year	Cost	Agency
Discovery and functional characterization of genic variants leading to Robinow syndrome and related skeletal dysplasias.	Fonseca, Claudia \| Sutton, Vernon R	2019	$118,875	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT
Discovery and functional characterization of genic variants leading to Robinow syndrome and related skeletal dysplasias.	Fonseca, Claudia \| Sutton, Vernon R	2018	$118,875	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT
LONGITUDINAL STUDY OF OSTEOPOROSIS IMPERFECTA	Sutton, Vernon R	2011	$11,477	NATIONAL CENTER FOR RESEARCH RESOURCES
LONGITUDINAL STUDY OF OSTEOPOROSIS IMPERFECTA	Sutton, Vernon R	2010	$5,723	NATIONAL CENTER FOR RESEARCH RESOURCES
CLINICAL PHENOTYPE OF IMPRINTED GENES ON CHROMOSOME 14	Sutton, Vernon R	2006	$2,171	NATIONAL CENTER FOR RESEARCH RESOURCES
Clinical Phenotype of Imprinted Genes of Chromosome 14	Sutton, Vernon R	2005	$121,008	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT
CLINICAL PHENOTYPE OF IMPRINTED GENES ON CHROMOSOME 14	Sutton, Vernon R	2005	$4,063	NATIONAL CENTER FOR RESEARCH RESOURCES
Clinical Phenotype of Imprinted Genes of Chromosome 14	Sutton, Vernon R	2004	$121,008	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT
Clinical Phenotype of Imprinted Genes on Chromosome 14	Sutton, Vernon R	2004	$2,981	NATIONAL CENTER FOR RESEARCH RESOURCES
Clinical Phenotype of Imprinted Genes of Chromosome 14	Sutton, Vernon R	2003	$121,008	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT
Clinical Phenotype of Imprinted Genes of Chromosome 14	Sutton, Vernon R	2002	$121,008	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT
Clinical Phenotype of Imprinted Genes of Chromosome 14	Sutton, Vernon R	2001	$121,008	EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT