Detalhe da pesquisa
1.
GRID1/GluD1 homozygous variants linked to intellectual disability and spastic paraplegia impair mGlu1/5 receptor signaling and excitatory synapses.
Mol Psychiatry
; 2024 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38418578
2.
Noncoding deletions reveal a gene that is critical for intestinal function.
Nature
; 571(7763): 107-111, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31217582
3.
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.
Am J Hum Genet
; 108(1): 115-133, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33308444
4.
ARF1-related disorder: phenotypic and molecular spectrum.
J Med Genet
; 60(10): 999-1005, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37185208
5.
Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy.
Hum Genet
; 142(5): 691-696, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36076104
6.
Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.
Am J Hum Genet
; 106(2): 246-255, 2020 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32004447
7.
Whole-exome sequencing reveals a monogenic cause in 56% of individuals with laterality disorders and associated congenital heart defects.
J Med Genet
; 59(7): 691-696, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34215651
8.
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities.
Genet Med
; 24(11): 2249-2261, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36074124
9.
PPP2R1A neurodevelopmental disorder is associated with congenital heart defects.
Am J Med Genet A
; 188(11): 3262-3277, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36209351
10.
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insights.
Pediatr Nephrol
; 37(7): 1623-1646, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34993602
11.
Mutations in PPCS, Encoding Phosphopantothenoylcysteine Synthetase, Cause Autosomal-Recessive Dilated Cardiomyopathy.
Am J Hum Genet
; 102(6): 1018-1030, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29754768
12.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.
Genet Med
; 23(10): 1922-1932, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34163037
13.
Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux-Lamy syndrome (MPS VI).
Am J Med Genet A
; 185(12): 3804-3809, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34435740
14.
The role of orotic acid measurement in routine newborn screening for urea cycle disorders.
J Inherit Metab Dis
; 44(3): 606-617, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33190319
15.
Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
Acta Haematol
; 144(3): 327-331, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-32980846
16.
Kidney and urinary tract findings among patients with Kabuki (make-up) syndrome.
Pediatr Nephrol
; 36(12): 4009-4012, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34570271
17.
Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome.
Am J Hum Genet
; 100(4): 666-675, 2017 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28318500
18.
Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability.
Am J Hum Genet
; 100(2): 257-266, 2017 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28132689
19.
A founder truncating variant in GDF1 causes autosomal-recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.
Am J Med Genet A
; 182(5): 987-993, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32144877
20.
Reversal of Intestinal Failure With Teduglutide in PERCC1-Associated Enteropathy: A Case Report.
Ann Intern Med
; 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710080