Search details
1.
Interaction network of human early embryonic transcription factors.
EMBO Rep
; 25(3): 1589-1622, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38297188
2.
Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs.
Genome Res
; 2022 Aug 12.
Article
in English
| MEDLINE | ID: mdl-35961773
3.
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.
Cereb Cortex
; 34(4)2024 Apr 01.
Article
in English
| MEDLINE | ID: mdl-38610086
4.
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Proc Natl Acad Sci U S A
; 119(35): e2202764119, 2022 08 30.
Article
in English
| MEDLINE | ID: mdl-35998220
5.
Primary cilia promote the differentiation of human neurons through the WNT signaling pathway.
BMC Biol
; 22(1): 48, 2024 Feb 27.
Article
in English
| MEDLINE | ID: mdl-38413974
6.
Embryonic LTR retrotransposons supply promoter modules to somatic tissues.
Genome Res
; 31(11): 1983-1993, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34675070
7.
Small RNA expression and miRNA modification dynamics in human oocytes and early embryos.
Genome Res
; 31(8): 1474-1485, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34340992
8.
The Continued Absence of Functional Germline Stem Cells in Adult Ovaries.
Stem Cells
; 41(2): 105-110, 2023 03 02.
Article
in English
| MEDLINE | ID: mdl-36153824
9.
Effects of exercise on whole-blood transcriptome profile in children with overweight/obesity.
Am J Hum Biol
; 36(2): e23983, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-37715654
10.
Long-term follow up of families with pathogenic NFKB1 variants reveals incomplete penetrance and frequent inflammatory sequelae.
Clin Immunol
; 246: 109181, 2023 01.
Article
in English
| MEDLINE | ID: mdl-36356849
11.
Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling.
J Clin Immunol
; 43(2): 358-370, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36260239
12.
A putative silencer variant in a spontaneous canine model of retinitis pigmentosa.
PLoS Genet
; 16(3): e1008659, 2020 03.
Article
in English
| MEDLINE | ID: mdl-32150541
13.
Differentiation of ciliated human midbrain-derived LUHMES neurons.
J Cell Sci
; 133(21)2020 11 09.
Article
in English
| MEDLINE | ID: mdl-33115758
14.
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
; 26(7): 3004-3017, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33057169
15.
Viral infection-related gene upregulation in monocytes in children with signs of ß-cell autoimmunity.
Pediatr Diabetes
; 23(6): 703-713, 2022 09.
Article
in English
| MEDLINE | ID: mdl-35419920
16.
Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants.
J Med Genet
; 58(7): 442-452, 2021 07.
Article
in English
| MEDLINE | ID: mdl-32709676
17.
Cystatin B-deficiency triggers ectopic histone H3 tail cleavage during neurogenesis.
Neurobiol Dis
; 156: 105418, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34102276
18.
A missense variant in IFT122 associated with a canine model of retinitis pigmentosa.
Hum Genet
; 140(11): 1569-1579, 2021 Nov.
Article
in English
| MEDLINE | ID: mdl-33606121
19.
FUT2 Variants Confer Susceptibility to Familial Otitis Media.
Am J Hum Genet
; 103(5): 679-690, 2018 11 01.
Article
in English
| MEDLINE | ID: mdl-30401457
20.
Microbial and transcriptional differences elucidate atopic dermatitis heterogeneity across skin sites.
Allergy
; 76(4): 1173-1187, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33001460