Detalles de la búsqueda
1.
Antiviral and Anti-Inflammatory Therapeutic Effect of RAGE-Ig Protein against Multiple SARS-CoV-2 Variants of Concern Demonstrated in K18-hACE2 Mouse and Syrian Golden Hamster Models.
J Immunol
; 212(4): 576-585, 2024 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38180084
2.
Experiences of hereditary cancer care among transgender and gender diverse people: "It's gender. It's cancer risk it's everything".
J Genet Couns
; 2024 Feb 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-38342966
3.
Beyond multiple choice: Clinical simulation as a rigorous and inclusive method for assessing genetic counseling competencies.
J Genet Couns
; 33(1): 118-123, 2024 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-38351603
4.
Antiviral CD19+CD27+ Memory B Cells Are Associated with Protection from Recurrent Asymptomatic Ocular Herpesvirus Infection.
J Virol
; 96(5): e0205721, 2022 03 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34985998
5.
Research participants' perspectives about the return of uninformative genomic test results in a clinical research setting.
J Genet Couns
; 2023 Aug 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-37641538
6.
Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations.
J Allergy Clin Immunol
; 150(4): 947-954, 2022 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35753512
7.
The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Am J Hum Genet
; 104(4): 578-595, 2019 04 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30951675
8.
Genomic tools for health: Secondary findings as findings to be shared.
Genet Med
; 24(11): 2220-2227, 2022 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-35980380
9.
Reason-Based Abortion Bans, Disability Rights, and the Future of Prenatal Genetic Testing.
Am J Law Med
; 48(2-3): 187-199, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36715254
10.
Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict.
J Genet Couns
; 30(3): 766-773, 2021 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-33320394
11.
An ethical framework for genetic counseling in the genomic era.
J Genet Couns
; 29(5): 718-727, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31856388
12.
Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions.
J Genet Couns
; 28(2): 304-312, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30680845
13.
National Society of Genetic Counselors' 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): 319-323, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35263009
14.
Clinical whole exome sequencing in child neurology practice.
Ann Neurol
; 76(4): 473-83, 2014 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25131622
15.
Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome.
Am J Med Genet A
; 167A(11): 2767-76, 2015 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-26174511
16.
'Out of hours' adult CT head interpretation by senior emergency department staff following an intensive teaching session: a prospective blinded pilot study of 405 patients.
Emerg Med J
; 31(6): 467-70, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23576233
17.
Queering genomics: How cisnormativity undermines genomic science.
HGG Adv
; 5(3): 100297, 2024 Apr 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-38637989
18.
Characterizing Decision-Making Surrounding Exercise in ARVC: Analysis of Decisional Conflict, Decisional Regret, and Shared Decision-Making.
Circ Genom Precis Med
; 16(6): e004133, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-38014565
19.
Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity.
Front Immunol
; 14: 1172004, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37215141
20.
The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome.
Blood Adv
; 6(13): 3974-3978, 2022 07 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35476126