V. Reid Sutton

13.7k citations

146 papers · 4.7k indexed · 1 hit paper · h-index 41

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders

Papers in

Clinical Biochemistry 35
- Metabolism and Genetic Disorders 35
Genetics 71
- Connective tissue disorders research 18
- Genomic variations and chromosomal abnormalities 18
- Genomics and Rare Diseases 14

Co-authors: Lisa G. Shaffer Sarah H. Elsea Qin Sun Ankita Patel James R. Lupski Adam D. Kennedy Marcus J. Miller Ignatia B. Van den Veyver
Journals: Molecular Genetics and Metabolism (18 papers)Genetics in Medicine (9 papers)The American Journal of Human Genetics (4 papers)American Journal of Medical Genetics Part A (27 papers)Clinical Genetics (3 papers)
Partner nations: United States Canada United Kingdom

In The Last Decade

V. Reid Sutton

141 papers receiving 4.6k citations

Hit Papers

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Asprosin, a Fasting-Induced Glucogenic Protein Hormone 2016 · 382 citations

Peers

Countries citing papers authored by V. Reid Sutton

Since Specialization

Citations

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

Fields of papers citing papers by V. Reid Sutton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. Reid Sutton. 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 V. Reid Sutton. The network helps show where V. Reid Sutton may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Setrusumab for the treatment of osteogenesis imperfecta: 12-month results from the phase 2b asteroid study Journal of Bone and Mineral Research ·Francis H. Glorieux, Bente Langdahl, Roland Chapurlat, Suzanne M. Jan de Beur, V. Reid Sutton, Kenneth Poole, Kathryn Dahir, Eric Orwoll, Bettina M. Willie, Nicholas Mikolajewicz, Elizabeth A. Zimmermann, Fernando Hoyos Salazar, Michael S. Ominsky, C. Stella Packiam, James Clancy, O Revka, Arun Mistry, M K Javaid	2024	9
2	Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn Screen International Journal of Neonatal Screening ·Diana Safitri Sri Kusuma, 真希市原, Mitchell E. Geffner, عبداللة سالم عبداللة, A. V. Koribut, V. Reid Sutton, Lefkothea Karaviti, Valérie Igounet, Mimi S. Kim	2023	1
3	Prenatal diagnosis of vascular anomalies Prenatal Diagnosis ·Shreya Agarwal, Amy R. Mehollin‐Ray, V. Reid Sutton, Ionela Iacobas	2023	5
4	Extremity anomalies associated with Robinow syndrome American Journal of Medical Genetics Part A ·Amjed Abu‐Ghname, Deny Nopriyanto, Matthew J. Davis, V. Reid Sutton, Chaofan Zhang, Shi Xiu-b, Claudia M.B. Carvalho, Renata S. Maricevich	2020	5
5	Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome American Journal of Medical Genetics Part A ·David D. Schwartz, V F Korsun, Claudia M.B. Carvalho, V. Reid Sutton, Juliana F. Mazzeu, Marni E. Axelrad	2020	6
6	Recessive ACO2 variants as a cause of isolated ophthalmologic phenotypes American Journal of Medical Genetics Part A ·E.V. Korotkikh, Mahshid S. Azamian, Seema R. Lalani, Kimberly G. Yen, V. Reid Sutton, Daryl A. Scott	2020	6
7	Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profiles Bone ·K. Leski, Marie‐Eve Robinson, Joe Renouard, V. Reid Sutton, Brendan Lee, Francis H. Glorieux, Frank Rauch	2020	10
8	Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome American Journal of Medical Genetics Part A ·Chaofan Zhang, Juliana F. Mazzeu, Jesper Eisfeldt, Christopher M. Grochowski, Janson J. White, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, Anna Lindstrand, James R. Lupski, V. Reid Sutton, Claudia M.B. Carvalho	2020	14
9	Characterization of the Robinow syndrome skeletal phenotype, bone micro‐architecture, and genotype–phenotype correlations with the osteosclerotic form American Journal of Medical Genetics Part A ·Brian J. Shayota, Chaofan Zhang, Roman J. Shypailo, Juliana F. Mazzeu, Claudia M.B. Carvalho, V. Reid Sutton	2020	4
10	Craniofacial phenotypes associated with Robinow syndrome American Journal of Medical Genetics Part A ·Bharathi Doddla Raghunathanaidu, Amjed Abu‐Ghname, 顾冰, Matthew J. Davis, Shi Xiu-b, V. Reid Sutton, Claudia M.B. Carvalho, Renata S. Maricevich	2020	4
11	Caries prevalence and experience in individuals with osteogenesis imperfecta: A cross‐sectional multicenter study Special Care in Dentistry ·Stephen P. Matava, 裕二隈, M. I. PLUSNIN, Arantxa Camus, Faleh Tamimi, 尚朝倉, Francis H. Glorieux, Brendan Lee, V. Reid Sutton, Frank Rauch, Shahrokh Esfandiari	2019	12
12	VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features Clinical Genetics ·Christian Beetz, Najim Ameziane, M. F. Michells, Vasiliki Karageorgou, Peter Bauer, Jehan Suleiman, V. Reid Sutton, Ayman W. El‐Hattab	2019	4
13	Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome) American Journal of Medical Genetics Part A ·Nurit Assia Batzir, Jennifer E. Posey, Xiaofei Song, Zeynep Coban‐Akdemir, Jill A. Rosenfeld, Chester Brown, Emily Chen, 王学信, Libas Phaiju, Moisés Muchinski, Katelyn Payne, Annick Raas‐Rothschild, Richard H. Scott, Hilary J. Vernon, Neda Zadeh, James R. Lupski, V. Reid Sutton	2019	30
14	Aicardi syndrome, an unsolved mystery: Review of diagnostic features, previous attempts, and future opportunities for genetic examination American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Bibiana K. Y. Wong, V. Reid Sutton	2018	19
15	Whole‐Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI JBMR Plus ·Zixue Jin, Lindsay C. Burrage, Ming‐Ming Jiang, 慶太速水, Terry Bertin, Yuqing Chen, Alyssa A. Tran, Richard A. Gibbs, Shalini N. Jhangiani, V. Reid Sutton, Frank Rauch, Brendan Lee, Mahim Jain	2018	3
16	Phenotypic and molecular characterization of focal dermal hypoplasia in 18 individuals American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Bret L. Bostwick, Ping Fang, Ankita Patel, V. Reid Sutton	2016	28
17	Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes American Journal of Medical Genetics Part A ·Lisa Emrick, Lauren Murphy, Alireza A. Shamshirsaz, Rodrigo Ruano, Christopher I. Cassady, Liu Liu, Fengqi Chang, V. Reid Sutton, Marilyn M. Li, Ignatia B. Van den Veyver	2014	25
18	Ophthalmological Manifestations of Focal Dermal Hypoplasia (Goltz syndrome): A Case Series of 18 patients Investigative Ophthalmology & Visual Science ·J. Hendrych, V. Reid Sutton	2014	1
19	P heno DB : A New Web‐Based Tool for the Collection, Storage, and Analysis of Phenotypic Features Human Mutation ·Ada Hamosh, Nara Sobreira, Julie Hoover‐Fong, V. Reid Sutton, Corinne D. Boehm, François Schiettecatte, David Valle	2013	48
20	De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome Genome Medicine ·Matthew N. Bainbridge, Hao Hu, Donna M. Muzny, Luciana Musante, James R. Lupski, Brett H. Graham, Wei Chen, Karen W. Gripp, Kim Jenny, Thomas F. Wienker, Yaping Yang, V. Reid Sutton, Richard A. Gibbs, Hans‐Hilger Ropers	2013	102

About V. Reid Sutton

V. Reid Sutton is a scholar working on Clinical Biochemistry, Genetics, Urology, Rheumatology and Pediatrics, Perinatology and Child Health, having authored 146 papers that have together received 4.7k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (35 papers), Connective tissue disorders research (18 papers), Genomic variations and chromosomal abnormalities (18 papers), Genomics and Rare Diseases (14 papers), Prenatal Screening and Diagnostics (13 papers), Metabolomics and Mass Spectrometry Studies (11 papers), Sexual Differentiation and Disorders (10 papers) and Lysosomal Storage Disorders Research (9 papers). The work is most often cited by research in Clinical Biochemistry (916 citations), Genetics (2.2k citations), Pediatrics, Perinatology and Child Health (770 citations), Molecular Biology (2.5k citations) and Physiology (730 citations). V. Reid Sutton has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Lisa G. Shaffer, Sarah H. Elsea, Qin Sun, Ankita Patel, James R. Lupski, Adam D. Kennedy, Marcus J. Miller, Ignatia B. Van den Veyver, Sau Wai Cheung and Lindsay C. Burrage. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, The American Journal of Human Genetics, American Journal of Medical Genetics Part A and Clinical Genetics.

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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