Detalhe da pesquisa
1.
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.
Nature
; 612(7940): 495-502, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450981
2.
Author Correction: Determination of RNA structural diversity and its role in HIV-1 RNA splicing.
Nature
; 588(7837): E16, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33214714
3.
Determination of RNA structural diversity and its role in HIV-1 RNA splicing.
Nature
; 582(7812): 438-442, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32555469
4.
Integrated genome and transcriptome analyses reveal the mechanism of genome instability in ataxia with oculomotor apraxia 2.
Proc Natl Acad Sci U S A
; 119(4)2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35042798
5.
Delayed DNA replication in haploid human embryonic stem cells.
Genome Res
; 31(12): 2155-2169, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34810218
6.
Impact of Regional Differences and Neighborhood Socioeconomic Deprivation on the Outcomes of Patients with Lower Extremity Wounds Evaluated by a Limb-Preservation Service.
J Vasc Surg
; 2024 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38782216
7.
Contemporary outcomes for arterial reconstruction with non-saphenous vein cryo-preserved conduits.
J Vasc Surg
; 79(6): 1457-1465, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38286153
8.
EED related overgrowth: First report of multiple members in a single family.
Am J Med Genet A
; 194(2): 374-382, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37840385
9.
Neuropathy Screening for Patients with Peripheral Vascular Disease Helps to Identify Those at an Increased Risk of Amputation, Revascularization, and Death.
Ann Vasc Surg
; 100: 60-66, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38128695
10.
Implementation strategies to support ultrasound thyroid nodule risk stratification: A systematic review.
Clin Endocrinol (Oxf)
; 99(4): 417-427, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37393196
11.
Contemporary outcomes for branch renal artery repair.
J Vasc Surg
; 78(1): 96-101, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36931612
12.
Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.
Am J Med Genet A
; 191(7): 1900-1910, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37183572
13.
Addressing the Increasing Mental Health Distress and Mental Illness Among Young Adults in the United States.
J Nerv Ment Dis
; 211(12): 961-967, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38015186
14.
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Circulation
; 144(1): 7-19, 2021 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33947203
15.
Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants.
Hum Mol Genet
; 29(4): 566-579, 2020 03 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31813956
16.
Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants.
Genet Med
; 24(1): 130-145, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906502
17.
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations.
Genet Med
; 24(9): 1952-1966, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35916866
18.
Confirmation and variability of the Allee effect inDictyostelium discoideumcell populations, possible role of chemical signaling within cell clusters.
Phys Biol
; 19(2)2022 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34942613
19.
Prevalence of chronic opioid use in patients with peripheral arterial disease undergoing revascularization.
J Vasc Surg
; 75(1): 186-194, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34478808
20.
Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics.
J Med Genet
; 58(9): 609-618, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33060286