Detalhe da pesquisa
1.
Assessment of Interprofessional Competence of Leadership Education in Neurodevelopmental and Related Disabilities Trainees through a Virtual Standardized Patient Encounter.
Matern Child Health J
; 28(1): 44-51, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37910329
2.
A qualitative assessment of parental experiences with false-positive newborn screening for Krabbe disease.
J Genet Couns
; 31(1): 252-260, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34265137
3.
Age of onset and behavioral manifestations in Huntington's disease: An Enroll-HD cohort analysis.
Clin Genet
; 99(1): 133-142, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33020896
4.
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.
Am J Med Genet A
; 185(6): 1649-1665, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33783954
5.
Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives.
Am J Med Genet A
; 182(1): 104-114, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31639281
6.
Maternal age at delivery and fertility of the next generation.
Paediatr Perinat Epidemiol
; 34(6): 629-636, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32150298
7.
An Unusual Cause of Diarrhea in Young Adulthood.
Gastroenterology
; 164(6): e1-e2, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36270335
8.
An assessment of health, social, communication, and daily living skills of adults with Down syndrome.
Am J Med Genet A
; 176(6): 1389-1397, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29696786
9.
Differential mutation frequencies in metastatic cutaneous squamous cell carcinomas versus primary tumors.
Cancer
; 123(7): 1184-1193, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27906449
10.
Patients with Amyotrophic Lateral Sclerosis Have High Interest in and Limited Access to Genetic Testing.
J Genet Couns
; 26(3): 604-611, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27761850
11.
Accreditation Council for Genetic Counseling Board of Directors Response to Myers et al 'A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination'.
J Genet Couns
; 31(2): 316-318, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35150179
12.
At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease.
J Genet Couns
; 26(4): 669-688, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28283918
13.
The Accreditation Council for Genetic Counseling's response to COVID-19 impact on genetic counseling programs.
J Genet Couns
; 30(4): 1046-1056, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34224607
14.
Allele-specific imbalance mapping identifies HDAC9 as a candidate gene for cutaneous squamous cell carcinoma.
Int J Cancer
; 134(1): 244-8, 2014 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23784969
15.
Models of service delivery for cancer genetic risk assessment and counseling.
J Genet Couns
; 23(2): 239-53, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24158360
16.
Germline variation controls the architecture of somatic alterations in tumors.
PLoS Genet
; 6(9): e1001136, 2010 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-20885788
17.
Erratum to: At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease.
J Genet Couns
; 26(4): 689, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28470398
18.
KMT2D loss drives aggressive tumor phenotypes in cutaneous squamous cell carcinoma.
Am J Cancer Res
; 12(3): 1309-1322, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35411237
19.
MicroRNA Expression Profiling of Cutaneous Squamous Cell Carcinomas Arising in Different Sites.
Otolaryngol Head Neck Surg
; 163(3): 538-545, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32423289
20.
Genetic counseling and testing for common hereditary breast cancer syndromes: a paper from the 2007 William Beaumont hospital symposium on molecular pathology.
J Mol Diagn
; 10(5): 383-95, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18687797