Detalhe da pesquisa
1.
Structurally divergent and recurrently mutated regions of primate genomes.
Cell
; 187(6): 1547-1562.e13, 2024 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38428424
2.
Increased mutation and gene conversion within human segmental duplications.
Nature
; 617(7960): 325-334, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37165237
3.
Assembly of 43 human Y chromosomes reveals extensive complexity and variation.
Nature
; 621(7978): 355-364, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612510
4.
The complete sequence of a human Y chromosome.
Nature
; 621(7978): 344-354, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612512
5.
A Family of Argonaute-Interacting Proteins Gates Nuclear RNAi.
Mol Cell
; 78(5): 862-875.e8, 2020 06 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32348780
6.
The structure, function and evolution of a complete human chromosome 8.
Nature
; 593(7857): 101-107, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33828295
7.
A high-quality bonobo genome refines the analysis of hominid evolution.
Nature
; 594(7861): 77-81, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33953399
8.
Familial long-read sequencing increases yield of de novo mutations.
Am J Hum Genet
; 109(4): 631-646, 2022 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35290762
9.
Targeted long-read sequencing identifies missing disease-causing variation.
Am J Hum Genet
; 108(8): 1436-1449, 2021 08 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34216551
10.
Facebook Online Support Groups for Hospice Family Caregivers of Advanced Cancer Patients: Protocol, Facilitation Skills and Promising Outcomes.
J Soc Work End Life Palliat Care
; 18(2): 146-159, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35282796
11.
A Phenomenological Exploration of the Voices Reported by Borderline Personality and Schizophrenia Patients.
Psychopathology
; 54(3): 159-168, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33975316
12.
Immune checkpoint inhibitors: a narrative review of considerations for the anaesthesiologist.
Br J Anaesth
; 124(3): 251-260, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32007241
13.
An objective methodology capturing online commodity marketing and other harms.
Health Promot Int
; 35(6): 1312-1319, 2020 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31986195
14.
Population-based genetic testing of asymptomatic women for breast and ovarian cancer susceptibility.
Genet Med
; 21(4): 913-922, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30254378
15.
The haplotype-resolved genome and epigenome of the aneuploid HeLa cancer cell line.
Nature
; 500(7461): 207-11, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23925245
16.
Pembrolizumab-induced Sarcoid-like Reactions during Treatment of Metastatic Melanoma.
Radiology
; 289(2): 564-567, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30106351
17.
Identification and treatment of offenders with attention-deficit/hyperactivity disorder in the prison population: a practical approach based upon expert consensus.
BMC Psychiatry
; 18(1): 281, 2018 09 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30180832
18.
Recurrent somatic loss of TNFRSF14 in classical Hodgkin lymphoma.
Genes Chromosomes Cancer
; 55(3): 278-87, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26650888
19.
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia.
Am J Hum Genet
; 92(1): 99-106, 2013 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23261302
20.
Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.
Am J Hum Genet
; 93(4): 711-20, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24055112