Victoria Carlton - Concepedia

Author

Victoria Carlton

Also Known As

Carlton, Victoria E H, V Carlton, V E Carlton, V. Carlton, V. E. H. Carlton, V.E.H. Carlton, Victoria Carlton, Victoria E H Carlton, Victoria E. Carlton, Victoria E. H. Carlton

Publications

7.6K

Citations

H-Index

Concepts

All Affiliations

University of California, San Francisco Adaptive Biotechnologies (United States)Stanford University Dana-Farber Cancer Institute The University of Texas MD Anderson Cancer Center

About

Victoria Carlton is an author at University of California, San Francisco specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	5.4K
2	Engineering	4	4	1.4K
3	Biostatistics	2	2	56
4	Computer Engineering	1	1	20
5	Computer Science	1	1	20

Victoria Carlton

Publications

7.4K

Citations

H-Index

Page 1

	Year	Citations
A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis Ann B. Begovich, Victoria Carlton, Lee Honigberg, The American Journal of Human Genetics Rheumatoid DisorderRheumatologyProtein Tyrosine PhosphataseAutoimmune DiseaseDisease Mechanism	2004	1.5K
Diverse somatic mutation patterns and pathway alterations in human cancers Zhengyan Kan, Bijay S. Jaiswal, Jeremy Stinson, Nature Cancer ResearchEngineeringPathway AlterationsSomatic VariantTumor Heterogeneity	2010	1K
Genetic Association of the R620W Polymorphism of Protein Tyrosine Phosphatase PTPN22 with Human SLE Chieko Kyogoku, Ward Ortmann, Annette Lee, The American Journal of Human Genetics Signal TransductionGenetic DisorderGeneticsGenetic EpidemiologyHuman Polymorphism	2004	658
Analysis of Families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: the PTPN22 620W Allele Associates with Multiple Autoimmune Phenotypes Lindsey A. Criswell, Kirsten A. Pfeiffer, Raymond F. Lum, The American Journal of Human Genetics Genome-wide Association StudyAllelic VariantAutoimmune DiseaseGeneticsImmunology	2005	599
Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia Malek Faham, Jianbiao Zheng, Martin Moorhead, Blood	2012	408
Minimal residual disease negativity using deep sequencing is a major prognostic factor in multiple myeloma Aurore Perrot, Valérie Lauwers‐Cancès, Jill Corre, Blood	2018	408
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT Victoria Carlton, Baruch Z. Harris, Erik G. Puffenberger, Nature Genetics Genetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyAssociated Mutations	2003	324
Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders Marco Ladetto, Monika Brüggemann, Luigia Monitillo, Leukemia Disease DiagnosisEngineeringAutoimmune DiseaseDisease ProgressionReal-time Quantitative Pcr	2013	303
Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): Evidence for heterogeneity L Bull, Victoria Carlton, N L Stricker, Hepatology GeneticsGenetic EpidemiologyByler DiseasePathologyMorphological Findings	1997	277
Antigen presentation profiling reveals recognition of lymphoma immunoglobulin neoantigens Michael S. Khodadoust, Niclas Olsson, Lisa E. Wagar, Nature Lymphoid NeoplasiaAutoimmune DiseaseMedicineImmunologyPathology	2017	260

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