Detalhe da pesquisa
1.
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Am J Hum Genet
; 110(9): 1454-1469, 2023 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595579
2.
The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature
; 581(7809): 434-443, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32461654
3.
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project.
Hum Genomics
; 18(1): 44, 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38685113
4.
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies.
Am J Hum Genet
; 108(5): 919-928, 2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33789087
5.
A form of muscular dystrophy associated with pathogenic variants in JAG2.
Am J Hum Genet
; 108(5): 840-856, 2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33861953
6.
Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort.
Genet Med
; 26(5): 101076, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38258669
7.
Unexpected frequency of the pathogenic AR CAG repeat expansion in the general population.
Brain
; 146(7): 2723-2729, 2023 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36797998
8.
seqr: A web-based analysis and collaboration tool for rare disease genomics.
Hum Mutat
; 43(6): 698-707, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35266241
9.
Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature
; 597(7874): E3-E4, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34373650
10.
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature
; 590(7846): E53, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33536625
11.
Analysis of protein-coding genetic variation in 60,706 humans.
Nature
; 536(7616): 285-91, 2016 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27535533
12.
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 15(5): e1008190, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31145742
13.
A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families.
Brain
; 143(10): 2904-2910, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33103729
14.
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.
PLoS Genet
; 14(5): e1007329, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29795570
15.
Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy.
Hum Mutat
; 41(2): 403-411, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31660661
16.
Variant Score Ranker-a web application for intuitive missense variant prioritization.
Bioinformatics
; 35(21): 4478-4479, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31086968
17.
A form of muscular dystrophy associated with pathogenic variants in JAG2.
Am J Hum Genet
; 108(6): 1164, 2021 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34087166
18.
The ExAC browser: displaying reference data information from over 60 000 exomes.
Nucleic Acids Res
; 45(D1): D840-D845, 2017 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27899611
19.
Pathogenic ASXL1 somatic variants in reference databases complicate germline variant interpretation for Bohring-Opitz Syndrome.
Hum Mutat
; 38(5): 517-523, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28229513
20.
KSHV 2.0: a comprehensive annotation of the Kaposi's sarcoma-associated herpesvirus genome using next-generation sequencing reveals novel genomic and functional features.
PLoS Pathog
; 10(1): e1003847, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24453964