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Author Details

Albert de la Chapelle
The Ohio State University Comprehensive Cancer Center
1961
661
117
PMIDPaper TitleJournal TitlePublished Year
33393477Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patients.Gynecol Oncol2021
33683341Gene expression signature predicts relapse in adult patients with cytogenetically normal acute myeloid leukemia.Blood Adv2021
33740060Genetically predicted circulating concentrations of micronutrients and risk of colorectal cancer among individuals of European descent: a Mendelian randomization study.Am J Clin Nutr2021
33667396Response to Li and Hopper.Am J Hum Genet2021
33527407Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.Int J Cancer2021
33632709Genetic architectures of proximal and distal colorectal cancer are partly distinct.Gut2021
34916535Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer.Nat Commun2021
34250417Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative.JCO Precis Oncol2021
34238982Transcriptome analysis discloses dysregulated genes in normal appearing tumor-adjacent thyroid tissues from patients with papillary thyroid carcinoma.Sci Rep2021
33943044A novel essential splice site variant in SPTB in a large hereditary spherocytosis family.Mol Genet Genomic Med2021
33277314Poor Survival and Differential Impact of Genetic Features of Black Patients with Acute Myeloid Leukemia.Cancer Discov2021
32132206Assessing thyroid cancer risk using polygenic risk scores.Proc Natl Acad Sci U S A2020
35047832Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis.HGG Adv2020
32024448Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in <i>APC</i>, <i>BRAF</i>, and <i>KTM2D</i>.Thyroid2020
31928178A Truncating Germline Mutation of <i>TINF2</i> in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres.Thyroid2020
31866242Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer.Gastroenterology2020
32051256Variants in <i>LRRC34</i> reveal distinct mechanisms for predisposition to papillary thyroid carcinoma.J Med Genet2020
31884074Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses.Gastroenterology2020
33203992Characterizing the function of EPB41L4A in the predisposition to papillary thyroid carcinoma.Sci Rep2020
32769997GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.Nat Commun2020
32758450Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.Am J Hum Genet2020
33020282Mutational landscape and clinical outcome of patients with de novo acute myeloid leukemia and rearrangements involving 11q23/<i>KMT2A</i>.Proc Natl Acad Sci U S A2020
32461631Additional gene mutations may refine the 2017 European LeukemiaNet classification in adult patients with de novo acute myeloid leukemia agedâ¿¿&lt;60 years.Leukemia2020
30510241Discovery of common and rare genetic risk variants for colorectal cancer.Nat Genet2019
31681970Clinical implications of GWAS variants associated with differentiated thyroid cancer.Endokrynol Pol2019
31375516Genetic Characterization and Prognostic Relevance of Acquired Uniparental Disomies in Cytogenetically Normal Acute Myeloid Leukemia.Clin Cancer Res2019
31275589Methylated <i>SEPTIN9</i> plasma test for colorectal cancer detection may be applicable to Lynch syndrome.BMJ Open Gastroenterol2019
31116161Neuroblastoma RAS viral oncogene homolog mRNA is differentially spliced to give five distinct isoforms: implications for melanoma therapy.Melanoma Res2019
30877237Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome.J Med Genet2019
30747051Microsatellite Instability Occurs in a Subset of Follicular Thyroid Cancers.Thyroid2019
30957677Identification of Rare Variants Predisposing to Thyroid Cancer.Thyroid2019
30350351Fine mapping of 14q13 reveals novel variants associated with different histological subtypes of papillary thyroid carcinoma.Int J Cancer2019
30679803Implementation of standardized variant-calling nomenclature in the age of next-generation sequencing: where do we stand?Leukemia2019
30654714Risk Haplotypes Uniquely Associated with Radioiodine-Refractory Thyroid Cancer Patients of High African Ancestry.Thyroid2019
30291333Genome-wide association study identifies an acute myeloid leukemia susceptibility locus near BICRA.Leukemia2019
29121253The Role of NRG1 in the Predisposition to Papillary Thyroid Carcinoma.J Clin Endocrinol Metab2018
30161022Cancer Risks for PMS2-Associated Lynch Syndrome.J Clin Oncol2018
29872168NF1 mutations are recurrent in adult acute myeloid leukemia and confer poor outcome.Leukemia2018
29768105Identification of a Recurrent LMO7-BRAF Fusion in Papillary Thyroid Carcinoma.Thyroid2018
29596542Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer.JAMA Oncol2018
29563537Mutation patterns identify adult patients with de novo acute myeloid leukemia aged 60 years or older who respond favorably to standard chemotherapy: an analysis of Alliance studies.Leukemia2018
29300379The role of SMAD3 in the genetic predisposition to papillary thyroid carcinoma.Genet Med2018
29027612Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.Fam Cancer2018
28031538Variants in microRNA genes in familial papillary thyroid carcinoma.Oncotarget2017
28336936No evidence for microsatellite instability in acute myeloid leukemia.Leukemia2017
28195142A genome-wide association study yields five novel thyroid cancer risk loci.Nat Commun2017
28321123The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.Leukemia2017
28466842Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.Nat Commun2017
29297870The early years of the ESHG leading to the reform of 1988 and the spirit of the Sestri Levante school.Eur J Hum Genet2017
28827320Identification of NRAS isoform 2 overexpression as a mechanism facilitating BRAF inhibitor resistance in malignant melanoma.Proc Natl Acad Sci U S A2017
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Collaborators

The Ohio State University Comprehensive Cancer Center, Comprehensive Cancer Center
Co-authored papers 62
The Ohio State University Comprehensive Cancer Center
Co-authored papers 43
Folkhalsan Research Center, University of Helsinki
Co-authored papers 35
Co-authored papers 32
The Ohio State University
Co-authored papers 27
Guardant Health Inc.
Co-authored papers 24
The Ohio State University Comprehensive Cancer Center
Co-authored papers 24
The Ohio State Comprehensive Cancer Center
Co-authored papers 21
Institut Francois Jacob, CNRS, Universite Paris-Saclay
Co-authored papers 20
Co-authored papers 18
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto
Co-authored papers 16
Mayo Clinic
Co-authored papers 16
The Ohio State University College of Medicine and Comprehensive Cancer Center
Co-authored papers 15
Co-authored papers 13
Biological and Chemical Research Centre, University of Warsaw
Co-authored papers 13
RIKEN Center for Integrative Medical Sciences
Co-authored papers 13
Dana Farber Cancer Institute
Co-authored papers 13
Mayo Clinic
Co-authored papers 12
Veracyte Inc.
Co-authored papers 10
Co-authored papers 9
Co-authored papers 9
Co-authored papers 9
Co-authored papers 9
German Cancer Research Center (DKFZ)
Co-authored papers 8
University of Iceland
Co-authored papers 8
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University of Southern California
Co-authored papers 8
Co-authored papers 8
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 8
University of Washington, USA Brotman Baty Institute for Precision Medicine
Co-authored papers 8