"Genetic Counseling" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An educational process that provides information and advice to individuals or families about a genetic condition that may affect them. The purpose is to help individuals make informed decisions about marriage, reproduction, and other health management issues based on information about the genetic disease, the available diagnostic tests, and management programs. Psychosocial support is usually offered.
Below are MeSH descriptors whose meaning is more general than "Genetic Counseling".
Below are MeSH descriptors whose meaning is more specific than "Genetic Counseling".
This graph shows the total number of publications written about "Genetic Counseling" by people in this website by year, and whether "Genetic Counseling" was a major or minor topic of these publications.
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|Year||Major Topic||Minor Topic||Total|
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Below are the most recent publications written about "Genetic Counseling" by people in Profiles.
Giri VN. When to use germline genetic testing in prostate cancer. Clin Adv Hematol Oncol. 2022 02; 20(2):78-81.
Mark JR, McDougall C, Giri VN. Genetic Testing Guidelines and Education of Health Care Providers Involved in Prostate Cancer Care. Urol Clin North Am. 2021 Aug; 48(3):311-322.
Arora V, Khan S, W El-Hattab A, Dua Puri R, Rocha ME, Merdzanic R, Paknia O, Beetz C, Rolfs A, Bertoli-Avella AM, Bauer P, Verma IC. Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal Agenesis. J Am Soc Nephrol. 2021 01; 32(1):223-228.
Hyatt C, Russo J, McDougall C. Genetic counseling perspective of engagement with urology and primary care. Can J Urol. 2019 Oct; 26(5 Suppl 2):52-53.
Gilstrop Thompson M, Corsetti S, Jain V, Ruhstaller K, Sciscione A. Accuracy of Routine Prenatal Genetic Screening in Patients Referred for Genetic Counseling. Am J Perinatol. 2020 02; 37(3):271-276.
Onoufriadis A, Nanda A, Sheriff A, Tomita K, Gomaa NS, Simpson MA, McGrath JA. Consanguinity and Double Recessive Gene Pathology: Cutis Laxa (PYCR1) and Nephrotic Syndrome (PLCE1). JAMA Dermatol. 2019 02 01; 155(2):257-259.
McGrath JA. The Molecular Revolution in Cutaneous Biology: Era of Molecular Diagnostics for Inherited Skin?Diseases. J Invest Dermatol. 2017 05; 137(5):e83-e86.
Scott RT. Introduction: Subchromosomal abnormalities in preimplantation embryonic aneuploidy screening. Fertil Steril. 2017 01; 107(1):4-5.
Treff NR, Franasiak JM. Detection of segmental aneuploidy and mosaicism in the human preimplantation embryo: technical considerations and limitations. Fertil Steril. 2017 01; 107(1):27-31.
Alderfer MA, Zelley K, Lindell RB, Novokmet A, Mai PL, Garber JE, Nathan D, Scollon S, Chun NM, Patenaude AF, Ford JM, Plon SE, Schiffman JD, Diller LR, Savage SA, Malkin D, Ford CA, Nichols KE. Parent decision-making around the genetic testing of children for germline TP53 mutations. Cancer. 2015 Jan 15; 121(2):286-93.