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Author Details
Full Name
Albert de la Chapelle
Affiliation
The Ohio State University Comprehensive Cancer Center
ORCID
Career Start Year
1961
Papers
661
H Index
117
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33393477
Double somatic mismatch repair gene pathogenic variants as common as Lynch syndrome among endometrial cancer patients.
Gynecol Oncol
2021
33683341
Gene expression signature predicts relapse in adult patients with cytogenetically normal acute myeloid leukemia.
Blood Adv
2021
33740060
Genetically predicted circulating concentrations of micronutrients and risk of colorectal cancer among individuals of European descent: a Mendelian randomization study.
Am J Clin Nutr
2021
33667396
Response to Li and Hopper.
Am J Hum Genet
2021
33527407
Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.
Int J Cancer
2021
33632709
Genetic architectures of proximal and distal colorectal cancer are partly distinct.
Gut
2021
34916535
Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer.
Nat Commun
2021
34250417
Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative.
JCO Precis Oncol
2021
34238982
Transcriptome analysis discloses dysregulated genes in normal appearing tumor-adjacent thyroid tissues from patients with papillary thyroid carcinoma.
Sci Rep
2021
33943044
A novel essential splice site variant in SPTB in a large hereditary spherocytosis family.
Mol Genet Genomic Med
2021
33277314
Poor Survival and Differential Impact of Genetic Features of Black Patients with Acute Myeloid Leukemia.
Cancer Discov
2021
32132206
Assessing thyroid cancer risk using polygenic risk scores.
Proc Natl Acad Sci U S A
2020
35047832
Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis.
HGG Adv
2020
32024448
Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in <i>APC</i>, <i>BRAF</i>, and <i>KTM2D</i>.
Thyroid
2020
31928178
A Truncating Germline Mutation of <i>TINF2</i> in Individuals with Thyroid Cancer or Melanoma Results in Longer Telomeres.
Thyroid
2020
31866242
Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer.
Gastroenterology
2020
32051256
Variants in <i>LRRC34</i> reveal distinct mechanisms for predisposition to papillary thyroid carcinoma.
J Med Genet
2020
31884074
Circulating 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.
Gastroenterology
2020
33203992
Characterizing the function of EPB41L4A in the predisposition to papillary thyroid carcinoma.
Sci Rep
2020
32769997
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.
Nat Commun
2020
32758450
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Am J Hum Genet
2020
33020282
Mutational 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 A
2020
32461631
Additional gene mutations may refine the 2017 European LeukemiaNet classification in adult patients with de novo acute myeloid leukemia agedâ¿¿<60 years.
Leukemia
2020
30510241
Discovery of common and rare genetic risk variants for colorectal cancer.
Nat Genet
2019
31681970
Clinical implications of GWAS variants associated with differentiated thyroid cancer.
Endokrynol Pol
2019
31375516
Genetic Characterization and Prognostic Relevance of Acquired Uniparental Disomies in Cytogenetically Normal Acute Myeloid Leukemia.
Clin Cancer Res
2019
31275589
Methylated <i>SEPTIN9</i> plasma test for colorectal cancer detection may be applicable to Lynch syndrome.
BMJ Open Gastroenterol
2019
31116161
Neuroblastoma RAS viral oncogene homolog mRNA is differentially spliced to give five distinct isoforms: implications for melanoma therapy.
Melanoma Res
2019
30877237
Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome.
J Med Genet
2019
30747051
Microsatellite Instability Occurs in a Subset of Follicular Thyroid Cancers.
Thyroid
2019
30957677
Identification of Rare Variants Predisposing to Thyroid Cancer.
Thyroid
2019
30350351
Fine mapping of 14q13 reveals novel variants associated with different histological subtypes of papillary thyroid carcinoma.
Int J Cancer
2019
30679803
Implementation of standardized variant-calling nomenclature in the age of next-generation sequencing: where do we stand?
Leukemia
2019
30654714
Risk Haplotypes Uniquely Associated with Radioiodine-Refractory Thyroid Cancer Patients of High African Ancestry.
Thyroid
2019
30291333
Genome-wide association study identifies an acute myeloid leukemia susceptibility locus near BICRA.
Leukemia
2019
29121253
The Role of NRG1 in the Predisposition to Papillary Thyroid Carcinoma.
J Clin Endocrinol Metab
2018
30161022
Cancer Risks for PMS2-Associated Lynch Syndrome.
J Clin Oncol
2018
29872168
NF1 mutations are recurrent in adult acute myeloid leukemia and confer poor outcome.
Leukemia
2018
29768105
Identification of a Recurrent LMO7-BRAF Fusion in Papillary Thyroid Carcinoma.
Thyroid
2018
29596542
Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer.
JAMA Oncol
2018
29563537
Mutation 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.
Leukemia
2018
29300379
The role of SMAD3 in the genetic predisposition to papillary thyroid carcinoma.
Genet Med
2018
29027612
Penetrance of a rare familial mutation predisposing to papillary thyroid cancer.
Fam Cancer
2018
28031538
Variants in microRNA genes in familial papillary thyroid carcinoma.
Oncotarget
2017
28336936
No evidence for microsatellite instability in acute myeloid leukemia.
Leukemia
2017
28195142
A genome-wide association study yields five novel thyroid cancer risk loci.
Nat Commun
2017
28321123
The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.
Leukemia
2017
28466842
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
Nat Commun
2017
29297870
The early years of the ESHG leading to the reform of 1988 and the spirit of the Sestri Levante school.
Eur J Hum Genet
2017
28827320
Identification of NRAS isoform 2 overexpression as a mechanism facilitating BRAF inhibitor resistance in malignant melanoma.
Proc Natl Acad Sci U S A
2017
1 - 50 of 661
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Collaborators
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The Ohio State University Comprehensive Cancer Center, Comprehensive Cancer Center
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The Ohio State University Comprehensive Cancer Center
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Folkhalsan Research Center, University of Helsinki
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35
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Co-authored papers
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The Ohio State University
Co-authored papers
27
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Guardant Health Inc.
Co-authored papers
24
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Co-authored papers
24
Krzysztof Mr??zek
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Co-authored papers
21
Jean Weissenbach
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Co-authored papers
20
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Co-authored papers
18
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Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital, University of Toronto
Co-authored papers
16
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Mayo Clinic
Co-authored papers
16
Matthew D Ringel
The Ohio State University College of Medicine and Comprehensive Cancer Center
Co-authored papers
15
Loic Le Marchand
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13
Krystian Jazdzewski
Biological and Chemical Research Centre, University of Warsaw
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13
Hidewaki Nakagawa
RIKEN Center for Integrative Medical Sciences
Co-authored papers
13
Richard M Stone
Dana Farber Cancer Institute
Co-authored papers
13
Noralane M Lindor
Mayo Clinic
Co-authored papers
12
Richard T Kloos
Veracyte Inc.
Co-authored papers
10
Laura G Brown
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9
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9
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9
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