Detalhe da pesquisa
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.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| MEDLINE | ID: mdl-30951675
8.
Genomic tools for health: Secondary findings as findings to be shared.
Genet Med
; 24(11): 2220-2227, 2022 11.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| MEDLINE | ID: mdl-33320394
11.
An ethical framework for genetic counseling in the genomic era.
J Genet Couns
; 29(5): 718-727, 2020 10.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| MEDLINE | ID: mdl-35263009
14.
Clinical whole exome sequencing in child neurology practice.
Ann Neurol
; 76(4): 473-83, 2014 Oct.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| MEDLINE | ID: mdl-23576233
17.
Queering genomics: How cisnormativity undermines genomic science.
HGG Adv
; 5(3): 100297, 2024 Apr 17.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| 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.
Artigo
Inglês
| MEDLINE | ID: mdl-35476126