Výsledky vyhledávání - "Lindsay Dohany"

Single Nucleotide Polymorphism-Based Chromosomal Microarray Evaluation of Hydatidiform Moles: A US National Reference Laboratory Experience

Autor: Fatih Z Boyar, Kylin Y. Lammers, Loretta W Mahon, Nicole Truitt, Arturo Anguiano, Lindsay Dohany, Boris T Wang

Publikováno v: Open Journal of Obstetrics and Gynecology. 10:1122-1134

Objectives: This retrospective study evaluated 1) benefits of single nucleotide polymorphism (SNP)-based chromosomal microarrays (CMAs) in the diagnosis of complete hydatidiform mole (CHM) and partial HM (PHM) in products of conception (POC) and amni

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::61730e7461a02c3c984c44d99ffbc837
https://doi.org/10.4236/ojog.2020.1080105

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Abstract P6-08-39: Hereditary cancer risk assessment using a chatbot in women presenting to obstetrics and gynecology practices across the U.S

Autor: Lindsay Dohany, Ashley Reeves, Heidi Owen, Christina Settler

Publikováno v: Cancer Research. 80:P6-08

Background: Hereditary cancer risk assessment is standard of care in the obstetrics and gynecology (ob/gyn) practice. Historical data indicates 1 in 12 individuals have a family history consistent with hereditary cancer(1), however recent data from a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e82e2c6247de7d264468e0283490d2b5
https://doi.org/10.1158/1538-7445.sabcs19-p6-08-39

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Clinical experience with multigene carrier panels in the reproductive setting

Autor: Ryan E. Longman, Carol Holland, Catherine Terhaar, Nicole Teed, Lindsay Dohany, Rachel Allen, Christina Settler

Publikováno v: Prenatal Diagnosis

Objectives Expanded carrier testing is acknowledged as an acceptable strategy for carrier testing by the American College of Obstetrics and Gynecology. Limited studies have investigated positivity rates of expanded carrier panels. We describe our exp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77be3f76ddea71f8f27ef1d32acf21f
https://doi.org/10.1002/pd.5272

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FMR1 premutation frequency in a large, ethnically diverse population referred for carrier testing

Autor: Christina Settler, Ryan E. Longman, Jeana DaRe, Tobias Mann, Carol Holland, Kailey M. Owens, Lindsay Dohany

Publikováno v: American Journal of Medical Genetics Part A. 176:1304-1308

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and is caused by an expansion of cytosine-guanine-guanine (CGG) repeats in the FMR1 gene. Female premutation allele carriers (55-200 CGG repeats) are at risk to ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a78ddc42fb206c31b56f77e4abf31a01
https://doi.org/10.1002/ajmg.a.38692

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Hereditary cancer testing in an ethnically diverse U.S. population

Autor: Nicholas Wisniewski, Stephanie Woods, Heidi Owen, Lindsay Dohany, Michele Basiliere, Lisa McDaniel

Publikováno v: Journal of Clinical Oncology. 39:10579-10579

10579 Background: The clinical utility of hereditary cancer multigene testing is well-established. Most testing has been performed in the White European population, with a relative shortage of data in other ethnic groups. Evaluation of hereditary can

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5eaf0a89595e982702b660cdc7973409
https://doi.org/10.1200/jco.2021.39.15_suppl.10579

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Abstract P4-12-13: Experience of pre-operative genetic testing on surgical decision making in newly diagnosed breast cancer patients

Autor: Heidi Dreyfuss, Dana Zakalik, Otavio Pereira-Rodrigues, Jennifer Fulbright, Ashley Reeves, Siddhartha Yadav, Lindsay Dohany

Publikováno v: Cancer Research. 75:P4-12

Introduction: BRCA 1 and 2 testing has been widely incorporated into clinical care for women at risk for hereditary breast cancer. Knowledge of BRCA mutation status prior to surgery may influence decision regarding type of surgery. This study analyze

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2712d1b1d1a295936143e2859613f5f8
https://doi.org/10.1158/1538-7445.sabcs14-p4-12-13

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To Reflex or Not: Additional BRCA1/2 Testing in Ashkenazi Jewish Individuals Without Founder Mutations

Autor: Jennifer Fulbright, Sarah Mange, Lindsay Dohany, Dana Zakalik, Debra Duquette, Nancie Petrucelli

Publikováno v: Journal of Genetic Counseling. 24:285-293

This study determined the prevalence of non-Ashkenazi Jewish BRCA1/2 mutations in the Ashkenazi Jewish population in the state of Michigan, current provider testing practices, and the use of mutation probability models in determining which Ashkenazi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a74720688d5df304a3ccc571e9a0e35d
https://doi.org/10.1007/s10897-014-9762-z

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Abstract P2-10-03: Impact of BRCA 1 and 2 Gene Mutation Testing on Surgical Decision-Making in Newly Diagnosed Breast Cancer Patients

Autor: A D'Souza, Dana Zakalik, Lindsay Dohany, Whitney Ducaine

Publikováno v: Cancer Research. 70:P2-10

BACKGROUND: Breast cancer patients with BRCA 1 or 2 gene mutations demonstrate a high lifetime incidence of a second breast cancer in the contralateral breast. These patients may benefit from a bilateral mastectomy (BLM) with an intent of risk reduct

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9a914edbf20fbbb1f1a6bb9f3e5f80a3
https://doi.org/10.1158/0008-5472.sabcs10-p2-10-03

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