George H. Thomas

4.2k citations

55 papers · 1.9k indexed · h-index 28

Molecular Biology top 10%
Genetics top 5%
Physiology top 5%
Clinical Biochemistry top 1%
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Linda Reynolds Carol S. Miller Harold A. Taylor Saul W. Brusilow Mark L. Batshaw Barbara R. Migeon William J. Mahoney G. Shashidhar Pai
Topics: Genomic variations and chromosomal abnormalities (15 papers)Metabolism and Genetic Disorders (13 papers)Lysosomal Storage Disorders Research (8 papers)
Cited by: Clinical Biochemistry Genetics Pediatrics, Perinatology and Child Health
Journals: Nature Science New England Journal of Medicine
Partner nations: United States Denmark Singapore

In The Last Decade

George H. Thomas

53 papers receiving 1.8k citations

Peers

Countries citing papers authored by George H. Thomas

Since Specialization

Citations

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

Fields of papers citing papers by George H. Thomas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by George H. Thomas. 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 George H. Thomas. The network helps show where George H. Thomas may publish in the future.

Co-authorship network of co-authors of George H. Thomas

This figure shows the co-authorship network connecting the top 25 collaborators of George H. Thomas. A scholar is included among the top collaborators of George H. Thomas 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 George H. Thomas. George H. Thomas 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	Genomic analysis of partial 21q monosomies with variable phenotypes 2010 ·European Journal of Human Genetics ·Elisha Roberson,Elizabeth Wohler,Julie Hoover‐Fong,Emily C. Lisi,Eric Stevens,George H. Thomas,Jay Leonard,Ada Hamosh,Jonathan Pevsner	44
2	Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: Evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular function 2009 ·American Journal of Medical Genetics Part A ·(unknown),Melonie A. Nance,Elizabeth Wohler,Julie Hoover‐Fong,Emily C. Lisi,George H. Thomas,Jonathan Pevsner	36
3	Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development 2008 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Nancy Braverman,Julie Hoover‐Fong,Claude J. Migeon,Denise Batista,George H. Thomas	14
4	3q29 interstitial microduplication: A new syndrome in a three‐generation family 2008 ·American Journal of Medical Genetics Part A ·Emily C. Lisi,Ada Hamosh,Kimberly F. Doheny,(unknown),Barbara L. Jackson,(unknown),George H. Thomas,Denise Batista	71
5	Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities 2007 ·The American Journal of Human Genetics ·Jorune Balciuniene,Ningping Feng,(unknown),Betsy Hirsch,Lawrence Charnas,Brent Bill,Mathew C. Easterday,Johan Staaf,(unknown),(unknown),Dimitri Avramopoulos,George H. Thomas,Åke Borg,David Valle‐García,Lisa A. Schimmenti,Scott B. Selleck	85
6	Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio 2007 ·Human Mutation ·Jason C. Ting,Elisha Roberson,(unknown),(unknown),Dietrich A. Stephan,George T. Capone,Ingo Ruczinski,George H. Thomas,Jonathan Pevsner	37
7	Optical determination of Cr(VI) using regenerable, functionalized sol–gel monoliths 2006 ·Analytica Chimica Acta ·(unknown),George H. Thomas,David Rodman,David B. Beach,Zi‐Ling Xue	41
8	A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9 2005 ·Genomics ·Simeon A. Boyadjiev,Sarah T. South,(unknown),Ankita Patel,George Zhang,David J. Hur,George H. Thomas,John P. Gearhart,Gail Stetten	21
9	Epitaxial Growth of Strontium Bismuth Tantalate/Niobate on Buffered Magnesium Oxide Substrates 2005 ·MRS Proceedings ·George H. Thomas,(unknown),Tolga Aytuğ,(unknown),David B. Beach	1
10	Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome 2002 ·American Journal of Medical Genetics ·Colyn B. Cargile,Denise Goh,Barbara K. Goodman,Xiaoning Chen,Julie R. Korenberg,Gregg L. Semenza,George H. Thomas	50
11	A novel variant three-way translocation of inversion 16 in a case of AML-M4eo following low dose methotrexate therapy 2001 ·Cancer Genetics and Cytogenetics ·Shiyong Li,Rima Couzi,George H. Thomas,Alan D. Friedman,Michael J. Borowitz	5
12	Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12) 2000 ·American Journal of Medical Genetics ·Colyn B. Cargile,Iain McIntosh,Mark V. Clough,Julie Rutberg,(unknown),Barbara K. Goodman,Xiao–Ning Chen,Julie R. Korenberg,George H. Thomas,Michael T. Geraghty	4
13	Molecular Cytogenetic Evaluation in a Patient with a Translocation (3;21) Associated with Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome (BPES) 2000 ·Genomics ·Verayuth Praphanphoj,Barbara K. Goodman,George H. Thomas,(unknown),Carmel Toomes,Michael J. Dixon,Michael T. Geraghty	44
14	Familial tandem duplication of bands q31.1 to q32.3 on chromosome 4 with mild phenotypic effect 1997 ·American Journal of Medical Genetics ·Barbara K. Goodman,George T. Capone,(unknown),George H. Thomas	26
15	Growing up with Patricia 1993 ·Pediatric Clinics of North America ·George H. Thomas,(unknown),Symme Trachtenberg	1
16	Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus 1990 ·New England Journal of Medicine ·Pamela Arn,Elizabeth R. Hauser,George H. Thomas,Gail E. Herman,David Hess,Saul W. Brusilow	140
17	Neuraminidase deficiency in the original patient with the Goldberg Syndrome 1979 ·Clinical Genetics ·George H. Thomas,Morton F. Goldberg,Carol S. Miller,Linda Reynolds	22
18	Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents 1976 ·The Journal of Pediatrics ·Arthur S. Aylsworth,Harold A. Taylor,(unknown),George H. Thomas	20
19	Hyperpipecolic acidemia associated with hepatomegaly, mental retardation, optic nerve dysplasia and progressive neurological disease 1975 ·Clinical Genetics ·George H. Thomas,Robert H. A. Haslam,Mark L. Batshaw,Arnold J. Capute,(unknown),(unknown)	84
20	Selected Screening Tests for Genetic Metabolic Diseases 1973 ·Medical Entomology and Zoology ·George H. Thomas,R. Rodney Howell	28

About George H. Thomas

George H. Thomas is a scholar working on Clinical Biochemistry, Genetics and Physiology, having authored 55 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Metabolism and Genetic Disorders (13 papers) and Lysosomal Storage Disorders Research (8 papers). The work is most often cited by research in Clinical Biochemistry (361 citations), Genetics (582 citations) and Pediatrics, Perinatology and Child Health (353 citations). George H. Thomas has collaborated with scholars based in United States, Denmark and Singapore. Frequent co-authors include Linda Reynolds, Carol S. Miller, Harold A. Taylor, Saul W. Brusilow, Mark L. Batshaw, Barbara R. Migeon, William J. Mahoney, G. Shashidhar Pai, Yuan Chuan Lee and Yoshihiro Uchida. Their work appears in journals such as Nature, Science and New England Journal of Medicine.

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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