Detalhe da pesquisa
1.
Solid organ transplantation after hematopoietic stem cell transplantation in childhood: A multicentric retrospective survey.
Am J Transplant
; 19(6): 1798-1805, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30586230
2.
Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans.
Nucleic Acids Res
; 44(8): 3750-62, 2016 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27060133
3.
Ex vivo drug sensitivity profiling-guided treatment of a relapsed pediatric mixed-phenotype acute leukemia with venetoclax and azacitidine.
Pediatr Blood Cancer
; 69(10): e29678, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35353439
4.
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Nature
; 478(7367): 97-102, 2011 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-21881559
5.
Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats.
PLoS Genet
; 10(6): e1004418, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24945355
6.
[Suspicion of constitutional abnormality at diagnosis of childhood leukemia: Update of the leukemia committee of the French Society of Childhood Cancers]. / Suspicion d'anomalie constitutionnelle au diagnostic de leucémie chez l'enfant : mise au point du comité leucémies de la Société française des cancers de l'enfant.
Bull Cancer
; 111(3): 291-309, 2024 Mar.
Artigo
em Francês
| MEDLINE | ID: mdl-38267311
7.
Rapid multiplexed genotyping of simple tandem repeats using capture and high-throughput sequencing.
Hum Mutat
; 34(9): 1304-11, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23696428
8.
[What are the genetic practices of SFCE oncopediatricians? A study of the CONECT-AML ethical group]. / Quelles sont les pratiques en génétique des pédiatres onco-hématologues de la SFCE ? Une enquête du groupe socle éthique CONECT-AML.
Bull Cancer
; 109(11): 1162-1176, 2022 Nov.
Artigo
em Francês
| MEDLINE | ID: mdl-36058716
9.
Type I hyperprolinemia: genotype/phenotype correlations.
Hum Mutat
; 31(8): 961-5, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20524212
10.
Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group.
Leukemia
; 37(8): 1723-1726, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37328541
11.
Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.
Plast Reconstr Surg
; 137(3): 952-961, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26910679
12.
Abundant contribution of short tandem repeats to gene expression variation in humans.
Nat Genet
; 48(1): 22-9, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26642241
13.
The emerging role of SHANK genes in neuropsychiatric disorders.
Dev Neurobiol
; 74(2): 113-22, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24124131
14.
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.
Arch Gen Psychiatry
; 66(9): 947-56, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19736351