Payal P Khincha

Payal P Khincha

UNVERIFIED PROFILE

Are you Payal P Khincha?   Register this Author

Register author
Payal P Khincha

Payal P Khincha

Publications by authors named "Payal P Khincha"

Are you Payal P Khincha?   Register this Author

20Publications

584Reads

10Profile Views

Reproductive factors associated with breast cancer risk in Li-Fraumeni syndrome.

Eur J Cancer 2019 Jul 15;116:199-206. Epub 2019 Jun 15.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, 9609, Medical Center Drive, MSC 9772, Bethesda, 20892, USA; Centro de Oncologia, Hospital Sirio-Libanes, Rua Dona Adma Jafet, 115- Bela Vista, Sao Paulo, Brazil.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejca.2019.05.005DOI Listing
July 2019

Variable population prevalence estimates of germline TP53 variants: A gnomAD-based analysis.

Hum Mutat 2019 01 19;40(1):97-105. Epub 2018 Nov 19.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/humu.23673
Publisher Site
http://dx.doi.org/10.1002/humu.23673DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6296902PMC
January 2019

Couples coping with screening burden and diagnostic uncertainty in Li-Fraumeni syndrome: Connection versus independence.

J Psychosoc Oncol 2019 Mar-Apr;37(2):178-193. Epub 2018 Dec 28.

a Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics , National Cancer Institute , Rockville , Maryland , USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/07347332.2018.1543376DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584025PMC
December 2018

Complex phenotype of dyskeratosis congenita and mood dysregulation with novel homozygous RTEL1 and TPH1 variants.

Am J Med Genet A 2018 06 25;176(6):1432-1437. Epub 2018 Apr 25.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), National Institutes of Health, Rockville, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.38706DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992073PMC
June 2018

Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenita.

Blood Adv 2018 06;2(11):1243-1249

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD; and.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/bloodadvances.2018016964DOI Listing
June 2018

Prevalence of Cancer at Baseline Screening in the National Cancer Institute Li-Fraumeni Syndrome Cohort.

JAMA Oncol 2017 12;3(12):1640-1645

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, Department of Health and Human Services, National Cancer Institute, National Institutes of Health, Bethesda, Maryland

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamaoncol.2017.1350DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5824271PMC
December 2017

Effect of pre-analytic variables on the reproducibility of qPCR relative telomere length measurement.

PLoS One 2017 8;12(9):e0184098. Epub 2017 Sep 8.

Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), Bethesda, Maryland, United States of America.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0184098PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590866PMC
October 2017

Correlation of Leukocyte Telomere Length Measurement Methods in Patients with Dyskeratosis Congenita and in Their Unaffected Relatives.

Int J Mol Sci 2017 Aug 13;18(8). Epub 2017 Aug 13.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3390/ijms18081765DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578154PMC
August 2017

Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.

Cancer 2016 Dec 6;122(23):3673-3681. Epub 2016 Aug 6.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/cncr.30248DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115949PMC
December 2016

Investigation of chromosome X inactivation and clinical phenotypes in female carriers of DKC1 mutations.

Am J Hematol 2016 12 4;91(12):1215-1220. Epub 2016 Nov 4.

Molecular and Cellular Pharmacology Group, Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.24545DOI Listing
December 2016

The limitations of qPCR telomere length measurement in diagnosing dyskeratosis congenita.

Mol Genet Genomic Med 2016 Jul 20;4(4):475-9. Epub 2016 Mar 20.

Clinical Genetics Branch Division of Cancer Epidemiology and Genetics National Cancer Institute, National Institutes of Health 9609 Medical Center Drive Rockville Maryland 20850.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mgg3.220DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947866PMC
July 2016

Neonatal manifestations of inherited bone marrow failure syndromes.

Semin Fetal Neonatal Med 2016 Feb 24;21(1):57-65. Epub 2015 Dec 24.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.siny.2015.12.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747853PMC
February 2016

Response to androgen therapy in patients with dyskeratosis congenita.

Br J Haematol 2014 May 12;165(3):349-57. Epub 2014 Feb 12.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD, USA; Children's National Medical Center, Washington, DC, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1111/bjh.12748
Publisher Site
http://dx.doi.org/10.1111/bjh.12748DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984599PMC
May 2014

Genomic characterization of the inherited bone marrow failure syndromes.

Semin Hematol 2013 Oct;50(4):333-47

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD; Children's National Medical Center, Washington, DC.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1053/j.seminhematol.2013.09.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3835370PMC
October 2013