Detalhe da pesquisa
1.
Adopted individuals' interest in elective genomic testing.
J Med Genet
; 59(2): 197-203, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33443090
2.
Pilot study of a culturally sensitive intervention to promote genetic counseling for breast cancer risk.
BMC Health Serv Res
; 22(1): 826, 2022 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35752812
3.
Development of a culturally sensitive narrative intervention to promote genetic counseling among African American women at risk for hereditary breast cancer.
Cancer
; 127(14): 2535-2544, 2021 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33794036
4.
Parental attitudes regarding the need for genetic services in a pediatric brain tumor survivorship program.
J Genet Couns
; 30(2): 533-543, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33073438
5.
Genetic counselors' perspectives on population-based screening for BRCA-related hereditary breast and ovarian cancer and Lynch syndrome.
J Genet Couns
; 30(1): 158-169, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32562467
6.
BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry.
Hum Mutat
; 40(10): 1781-1796, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31112363
7.
A feasibility study of breast cancer genetic risk assessment in a federally qualified health center.
Cancer
; 124(18): 3733-3741, 2018 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30320429
8.
Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome.
Blood
; 125(15): 2359-69, 2015 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-25608561
9.
Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
Blood
; 122(8): 1487-93, 2013 Aug 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-23847193
10.
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome.
J Am Soc Nephrol
; 25(1): 55-64, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24029428
11.
Allelic variants of complement genes associated with dense deposit disease.
J Am Soc Nephrol
; 22(8): 1551-9, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21784901
12.
A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome.
Nephrol Dial Transplant
; 26(2): 739-41, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20974643
13.
Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome.
Hum Mutat
; 31(6): E1445-60, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20513133
14.
A novel mutation in the complement factor B gene (CFB) and atypical hemolytic uremic syndrome.
Pediatr Nephrol
; 25(5): 947-51, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20108004
15.
Nm23-H1 suppresses tumor cell motility by down-regulating the lysophosphatidic acid receptor EDG2.
Cancer Res
; 67(15): 7238-46, 2007 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17671192
16.
Advantages and Some Remaining Challenges in Hereditary Gastrointestinal Cancer Panel Testing.
Clin Transl Gastroenterol
; 8(5): e92, 2017 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28492537
17.
An Eye on Trafficking Genes: Identification of Four Eye Color Mutations in Drosophila.
G3 (Bethesda)
; 6(10): 3185-3196, 2016 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27558665