Detalhe da pesquisa
1.
Germline genome modification through novel political, ethical, and social lenses.
PLoS Genet
; 17(9): e1009741, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34499641
2.
Novel Autoantibodies in Idiopathic Small Fiber Neuropathy.
Ann Neurol
; 91(1): 66-77, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34761434
3.
Expanding the genetic causes of small-fiber neuropathy: SCN genes and beyond.
Muscle Nerve
; 67(4): 259-271, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36448457
4.
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case report.
BMC Pediatr
; 22(1): 601, 2022 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36253810
5.
The orphan nuclear receptor NR0B2 could be a novel susceptibility locus associated with microsatellite-stable, APC mutation-negative early-onset colorectal carcinomas with metabolic manifestation.
Genes Chromosomes Cancer
; 60(2): 61-72, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33094510
6.
Ethical considerations of preconception and prenatal gene modification in the embryo and fetus.
Hum Reprod
; 36(12): 3018-3027, 2021 11 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34665851
7.
Design of Split Proximity Circuit as a Plug-and-Play Translator for Point Mutation Discrimination.
Anal Chem
; 92(16): 11164-11170, 2020 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32605366
8.
Development of clinical genetics in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 150-154, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31037834
9.
Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 155-165, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31050142
10.
Mutational spectrum of dystrophinopathies in Singapore: Insights for genetic diagnosis and precision therapy.
Am J Med Genet C Semin Med Genet
; 181(2): 230-244, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31081998
11.
Training in clinical genetics and genetic counseling in Asia.
Am J Med Genet C Semin Med Genet
; 181(2): 177-186, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31037827
12.
Delay discounting, genetic sensitivity, and leukocyte telomere length.
Proc Natl Acad Sci U S A
; 113(10): 2780-5, 2016 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-26903639
13.
J'Accuse .. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing.
Hum Genomics
; 16(1): 44, 2022 Sep 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36171619
14.
Genetic variation in CD38 and breastfeeding experience interact to impact infants' attention to social eye cues.
Proc Natl Acad Sci U S A
; 112(39): E5434-42, 2015 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26371313
15.
Association between the dopamine D4 receptor gene exon III variable number of tandem repeats and political attitudes in female Han Chinese.
Proc Biol Sci
; 282(1813): 20151360, 2015 Aug 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26246555
16.
Gold nanostructures for the multiplex detection of glucose-6-phosphate dehydrogenase gene mutations.
Anal Biochem
; 451: 56-62, 2014 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24491445
17.
Embryo and fetal gene editing: Technical challenges and progress toward clinical applications.
Mol Ther Methods Clin Dev
; 32(2): 101229, 2024 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38533521
18.
A clinical approach to diagnosis and management of mitochondrial myopathies.
Neurotherapeutics
; 21(1): e00304, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38241155
19.
Spinal muscular atrophy: from gene discovery to clinical trials.
Ann Hum Genet
; 77(5): 435-63, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23879295
20.
Genetics in Ischemic Stroke: Current Perspectives and Future Directions.
J Cardiovasc Dev Dis
; 10(12)2023 Dec 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38132662