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Victoria Carlton | Researchclopedia

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Victoria Carlton

87

Works

7,605

Citations

31

h-index

40

i10-index

Research Topics

Cancer Genomics and Diagnostics Lymphoma Diagnosis and Treatment Acute Lymphoblastic Leukemia research

Affiliations

San Francisco General Hospital2003–2003

University of Vienna2003–2003

University of California, San Francisco1995–2003

Universität Innsbruck2003–2003

Adaptive Biotechnologies (United States)2015–2018

Top Works

A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

Ann B. Begovich,Victoria Carlton,et al.

20041,500 citations

Monoclonal and Polyclonal Antibodies Research

Multiple Myeloma Research and Treatments

Diverse somatic mutation patterns and pathway alterations in human cancers

Zhengyan Kan,Bijay S. Jaiswal,et al.

20101,025 citations

Genetic Association of the R620W Polymorphism of Protein Tyrosine Phosphatase PTPN22 with Human SLE

Chieko Kyogoku,Ward Ortmann,et al.

2004662 citations

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,et al.

2005600 citations

Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia

Malek Faham,Jianbiao Zheng,et al.

2012420 citations

Minimal residual disease negativity using deep sequencing is a major prognostic factor in multiple myeloma

Aurore Perrot,Valérie Lauwers‐Cancès,et al.

2018412 citations

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT

Victoria Carlton,Baruch Z. Harris,et al.

2003324 citations

Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders

Marco Ladetto,Monika Brüggemann,et al.

2013303 citations

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): Evidence for heterogeneity

L Bull,Victoria Carlton,et al.

1997277 citations