Search details
1.
The Lancet Commission on the future of care and clinical research in autism.
Lancet
; 399(10321): 271-334, 2022 01 15.
Article
in English
| MEDLINE | ID: mdl-34883054
2.
Childhood acute myeloid leukemia shows a high level of germline predisposition.
Blood
; 138(22): 2293-2298, 2021 12 02.
Article
in English
| MEDLINE | ID: mdl-34521114
3.
BAM-matcher: a tool for rapid NGS sample matching.
Bioinformatics
; 32(17): 2699-701, 2016 09 01.
Article
in English
| MEDLINE | ID: mdl-27153667
4.
Resensitising proteasome inhibitor-resistant myeloma with sphingosine kinase 2 inhibition.
Neoplasia
; 24(1): 1-11, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34826777
5.
A Phase II Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy, Safety, and Tolerability of Arbaclofen Administered for the Treatment of Social Function in Children and Adolescents With Autism Spectrum Disorders: Study Protocol for AIMS-2-TRIALS-CT1.
Front Psychiatry
; 12: 701729, 2021.
Article
in English
| MEDLINE | ID: mdl-34504446
6.
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer.
Leukemia
; 35(11): 3245-3256, 2021 11.
Article
in English
| MEDLINE | ID: mdl-33850299
7.
Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia.
Leukemia
; 34(8): 2051-2063, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32076119
8.
Access to Dental Visits and Correlates of Preventive Dental Care in Children with Autism Spectrum Disorder.
J Autism Dev Disord
; 50(10): 3739-3747, 2020 Oct.
Article
in English
| MEDLINE | ID: mdl-32112232
9.
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.
Blood Adv
; 4(6): 1131-1144, 2020 03 24.
Article
in English
| MEDLINE | ID: mdl-32208489
10.
The Genomic Landscape of Sporadic Prolactinomas.
Endocr Pathol
; 30(4): 318-328, 2019 Dec.
Article
in English
| MEDLINE | ID: mdl-31473917
11.
The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution.
Leukemia
; 33(12): 2842-2853, 2019 12.
Article
in English
| MEDLINE | ID: mdl-31089247
12.
Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome.
Nat Rev Drug Discov
; 17(4): 280-299, 2018 04.
Article
in English
| MEDLINE | ID: mdl-29217836
13.
Arbaclofen in Children and Adolescents with Autism Spectrum Disorder: A Randomized, Controlled, Phase 2 Trial.
Neuropsychopharmacology
; 42(7): 1390-1398, 2017 Jun.
Article
in English
| MEDLINE | ID: mdl-27748740
14.
ASXL1 and BIM germ line variants predict response and identify CML patients with the greatest risk of imatinib failure.
Blood Adv
; 1(18): 1369-1381, 2017 Aug 08.
Article
in English
| MEDLINE | ID: mdl-29296778
15.
Clinical trial strategies for rare neurodevelopmental disorders: challenges and opportunities.
Nat Rev Drug Discov
; 20(9): 653-654, 2021 09.
Article
in English
| MEDLINE | ID: mdl-34002058
16.
Distal ventriculoperitoneal shunt failure caused by silicone allergy. Case report.
J Neurosurg
; 102(3): 536-9, 2005 Mar.
Article
in English
| MEDLINE | ID: mdl-15796391
17.
Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.
Child Neuropsychol
; 11(1): 109-17, 2005 Feb.
Article
in English
| MEDLINE | ID: mdl-15846854
18.
Language development in preschool-age children adopted from China.
J Speech Lang Hear Res
; 48(1): 93-107, 2005 Feb.
Article
in English
| MEDLINE | ID: mdl-15938062
19.
Local drug delivery to the brain.
Adv Drug Deliv Rev
; 54(7): 987-1013, 2002 Oct 16.
Article
in English
| MEDLINE | ID: mdl-12384318
20.
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.
Am J Psychiatry
; 161(9): 1700-2, 2004 Sep.
Article
in English
| MEDLINE | ID: mdl-15337663