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V. Carlton · SciRah

Researcher profile · Semantic Scholar

V. Carlton

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V. Carlton — researcher profile on SciRah

h-index: 28
Works: 72
Citations: 5,939

Most-cited papers

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.
A. Begovich, V. Carlton, L. Honigberg, Steven J. Schrodi +24 more
2004American Journal of Human Genetics1,590 citations Open access
Semantic Scholar
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.
C. Kyogoku, C. Langefeld, W. Ortmann, Annette Lee +18 more
2004American Journal of Human Genetics707 citations Open access
Semantic Scholar
Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia.
M. Faham, Jianbiao Zheng, M. Moorhead, V. Carlton +4 more
2012Blood418 citations Open access
Semantic Scholar
Minimal residual disease negativity using deep sequencing is a major prognostic factor in multiple myeloma.
A. Perrot, V. Lauwers-Cancès, J. Corre, N. Robillard +36 more
2018Blood383 citations Open access
Semantic Scholar
Next-generation sequencing and real-time quantitative PCR for minimal residual disease detection in B-cell disorders
M. Ladetto, M. Brüggemann, L. Monitillo, S. Ferrero +13 more
2014Leukemia299 citations Open access
Semantic Scholar
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT
V. Carlton, Baruch Z. Harris, E. Puffenberger, A. Batta +8 more
2003Nature Genetics297 citations
Semantic Scholar
Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC‐1] and Byler syndrome): Evidence for heterogeneity
L. Bull, V. Carlton, N. L. Stricker, S. Baharloo +19 more
1997Hepatology266 citations Open access
Semantic Scholar
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
V. Carlton, Xiaolan Hu, A. Chokkalingam, Steven J. Schrodi +14 more
2005American Journal of Human Genetics243 citations Open access
Semantic Scholar
Antigen Presentation Profiling Reveals Recognition of Lymphoma Immunoglobulin Neoantigens
M. Khodadoust, N. Olsson, Lisa E. Wagar, O. Haabeth +22 more
2017Nature240 citations Open access
Semantic Scholar
Immunoglobulin and T-cell receptor gene high-throughput sequencing quantifies minimal residual disease in acute lymphoblastic leukemia and predicts post-transplant relapse and survival
A. Logan, N. Vashi, M. Faham, V. Carlton +9 more
2014Biology of Blood and Marrow Transplantation143 citations Open access
Semantic Scholar
Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region.
V. Carlton, A. Knisely, N. Freimer
1995Human Molecular Genetics134 citations
Semantic Scholar
Minimal residual disease quantification using consensus primers and high-throughput IGH sequencing predicts post-transplant relapse in chronic lymphocytic leukemia
A. Logan, Bing Zhang, Balasubramanian Narasimhan, V. Carlton +8 more
2013Leukemia132 citations Open access
Semantic Scholar
Massive evolution of the immunoglobulin heavy chain locus in children with B precursor acute lymphoblastic leukemia.
C. Gawad, F. Pépin, V. Carlton, M. Klinger +5 more
2012Blood128 citations Open access
Semantic Scholar
Discovery of T Cell Receptor β Motifs Specific to HLA–B27–Positive Ankylosing Spondylitis by Deep Repertoire Sequence Analysis
M. Faham, V. Carlton, M. Moorhead, Jianbiao Zheng +9 more
2017Arthritis & Rheumatology105 citations Open access
Semantic Scholar
High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays
Yuk-Er Wang, V. Carlton, G. Karlin-Neumann, R. Sapolsky +15 more
2009BMC Medical Genomics102 citations Open access
Semantic Scholar
The prognostic value of clonal heterogeneity and quantitative assessment of plasma circulating clonal IG-VDJ sequences at diagnosis in patients with follicular lymphoma
C. Sarkozy, S. Huet, V. Carlton, B. Fabiani +8 more
2017OncoTarget87 citations Open access
Semantic Scholar
Next-Generation Sequencing-Based Detection of Circulating Tumour DNA After Allogeneic Stem Cell Transplantation for Lymphoma
A. Herrera, Haesook T. Kim, Katherine A. Kong, M. Faham +15 more
2016British Journal of Haematology60 citations Open access
Semantic Scholar
Prognostic value of sequencing-based minimal residual disease detection in patients with multiple myeloma who underwent autologous stem-cell transplantation
H. Takamatsu, N. Takezako, Jianbiao Zheng, M. Moorhead +16 more
2017Annals of Oncology46 citations Open access
Semantic Scholar
Detection of classical Hodgkin lymphoma specific sequence in peripheral blood using a next-generation sequencing approach
Y. Oki, S. Neelapu, M. Fanale, Larry W. Kwak +8 more
2015British Journal of Haematology46 citations Open access
Semantic Scholar
Molecular basis of intrahepatic cholestasis
V. Carlton, Ludmila Pawlikowska, L. Bull
2004Annals medicus42 citations Open access
Semantic Scholar
Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC
L. Bull, J. A. Juijn, M. Liao, M. V. van Eijk +22 more
1999Human Genetics39 citations Open access
Semantic Scholar
Open Access Methodology Article Prediction of Epigenetically Regulated Genes in Breast Cancer Cell Lines
Leandro A. Loss, A. Sadanandam, S. Durinck, S. Nautiyal +8 more
38 citations
Semantic Scholar
Evaluation of Minimal Residual Disease (MRD) in Relapsed/Refractory Multiple Myeloma (RRMM) Patients Treated with Daratumumab in Combination with Lenalidomide Plus Dexamethasone or Bortezomib Plus Dexamethasone
H. Avet-Loiseau, T. Casneuf, Christopher Chiu, J. Laubach +15 more
201636 citations
Semantic Scholar
Functional single nucleotide polymorphism-based association studies
V. Carlton, J. Ireland, F. Useche, M. Faham
2006Human Genomics35 citations Open access
Semantic Scholar
High-throughput method for analyzing methylation of CpGs in targeted genomic regions
S. Nautiyal, V. Carlton, Yontao Lu, J. Ireland +7 more
2010Proceedings of the National Academy of Sciences of the United States of America34 citations Open access
Semantic Scholar
Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64
R. Sinke, V. Carlton, J. A. Juijn, T. Delhaas +12 more
1997Human Genetics34 citations Open access
Semantic Scholar
The prognostic value of the depth of response in multiple myeloma depends on the time of assessment, risk status and molecular subtype
C. Schinke, A. Hoering, Hongwei Wang, V. Carlton +27 more
2017Haematologica30 citations Open access
Semantic Scholar
Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome.
M. Frühwirth, A. Janecke, Thomas Müller, V. Carlton +13 more
2003Jornal de Pediatria29 citations
Semantic Scholar
Nonsynonymous Coding Single-Nucleotide Polymorphisms Spanning the Genome in Relation to Glioblastoma Survival and Age at Diagnosis
M. Wrensch, A. Mcmillan, J. Wiencke, J. Wiemels +8 more
2007Clinical Cancer Research26 citations Open access
Semantic Scholar
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD)
S. Bentivegna, Jianbiao Zheng, Eugeni A. Namsaraev, V. Carlton +10 more
2008Human Mutation22 citations Open access
Semantic Scholar
High-throughput, high-accuracy array-based resequencing
Jianbiao Zheng, M. Moorhead, Li Weng, F. Siddiqui +10 more
2009Proceedings of the National Academy of Sciences of the United States of America19 citations Open access
Semantic Scholar
Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups
J. Ireland, V. Carlton, M. Falkowski, M. Moorhead +7 more
2006Human Genetics16 citations
Semantic Scholar
CANCER VACCINES AND T CELL THERAPY
K. Rezvani, J. Brody, H. Kohrt, A. Logan +8 more
2012Biology of Blood and Marrow Transplantation15 citations Open access
Semantic Scholar
A comparison of minimal residual disease detection in autografts among ASO‐qPCR, droplet digital PCR, and next‐generation sequencing in patients with multiple myeloma who underwent autologous stem cell transplantation
H. Takamatsu, R. Wee, Yoshitaka Zaimoku, R. Murata +18 more
2018British Journal of Haematology13 citations Open access
Semantic Scholar
Deep Sequencing Reveals Oligoclonality At The Immunoglobulin Locus In Multiple Myeloma Patients
J. Martínez-López, M. Fulciniti, S. Barrio, V. Carlton +7 more
201311 citations
Semantic Scholar
Genetic Variation : Evidence for Multiple Variants Associated with Rheumatoid Arthritis
V. Carlton, Xiaolan Hu, A. Chokkalingam, Steven J. Schrodi +14 more
20058 citations
Semantic Scholar
Next-Generation Sequencing and Real-Time Quantitative PCR for Minimal Residual Disease (MRD) Detection Using the Immunoglobulin Heavy Chain Variable Region: A Methodical Comparison in Acute Lymphoblastic Leukemia (ALL), Mantle Cell Lymphoma (MCL) and Multiple Myeloma (MM)
M. Ladetto, M. Brüggemann, S. Ferrero, F. Pépin +9 more
20127 citations
Semantic Scholar
A Genomic-Profile Derived Summary Measure of Chromosomal Breakpoints Predicts Response to Treatment with the DNA-Damaging Agent Cisplatin.
N. Juul, Yuk-Er Wang, Jeeyun Kim, A. Eklund +10 more
20096 citations
Semantic Scholar
Highly efficient somatic-mutation identification using Escherichia coli mismatch-repair detection
B. Peters, Zheng-Yan Kan, Dragan Sebisanovic, Kanan D. Pujara +14 more
2007Nature Methods6 citations
Semantic Scholar
Quantitative Assessment of Circulating Clonal IG-VDJ Sequences in Plasma of Follicular Lymphoma at Diagnosis Is Highly Predictive of Progression Free Survival (PFS)
C. Sarkozy, S. Huet, V. Carlton, A. Delmer +4 more
20155 citations
Semantic Scholar
Highly Sensitive Detection of Minimal Residual Disease in Acute Lymphoblastic Leukemia Using Next-Generation Sequencing of Immunoglobulin Heavy Chain Variable Region
M. Faham, T. Willis, M. Moorhead, V. Carlton +2 more
20115 citations
Semantic Scholar
Assessment of Central Nervous System Involvement in Pediatric Acute Lymphoblastic Leukemia Patients Using Next-Generation Sequencing Method
J. Choi, S. Jeha, Jianbiao Zheng, V. Carlton +2 more
20144 citations
Semantic Scholar
Detection Of Classical Hodgkin Lymphoma In Peripheral Blood Using High-Throughput Sequencing Assay
S. Neelapu, M. Fanale, L. Kwak, L. Fayad +6 more
20134 citations
Semantic Scholar
Deep B and T Cell Repertoire Sequencing to Evaluate Minimal Residual Disease and T Cell Responses in a Therapeutic Vaccine Trial for Mantle Cell Lymphoma
M. Faham, J. Brody, H. Kohrt, A. Logan +6 more
20124 citations
Semantic Scholar
High serum and urinary unconjugated bile acid concentrations are associated with homozygous mutation in bile acid coenzyme A: Amino acid N-acyltransferase (BAAT)
E. Barbarito, A. Batta, G. Salen, Homes D. Morton +3 more
20034 citations
Semantic Scholar
Next-Generation Sequencing Based Minimal Residual Disease Assessment in Peripheral Blood RNA from Multiple Myeloma Patients
J. Wolf, Katherine A. Kong, J. Wilmoth, J. Bayes +4 more
20163 citations
Semantic Scholar
A Novel Evolutionary Pattern Revealed Using Deep Sequencing of Immunoglobulin Loci at Diagnosis and over the Course of Treatment in Multiple Myeloma Patients
N. Munshi, J. Martínez-López, V. Carlton, S. Minvielle +10 more
20163 citations
Semantic Scholar
An algorithm to detect abnormal mRNA splicing and assess its clinical impact in individuals undergoing genetic testing for hereditary cancer syndromes
Nick Kamps-Hughes, V. Carlton, L. Frésard, Steve Osazuwa +5 more
2022bioRxiv2 citations Open access
Semantic Scholar
Comparison of MRD Detection By MFC, NGS and PET-CT in Patients at Different Treatment Stages for Multiple Myeloma
Sandra Susanibar, V. Carlton, S. Thanendrarajan, M. Mohan +10 more
20162 citations Open access
Semantic Scholar
Next-Generation Sequencing Reveals Clonal Evolution at the Immunoglobulin Loci in Chronic Lymphocytic Leukemia
Jennifer R. Brown, S. Fernandes, Siddha N. Kasar, K. Hoang +5 more
20142 citations
Semantic Scholar

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