Detalhe da pesquisa
1.
How Do We Recognize a Face?
Cell
; 169(6): 975-977, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28575674
2.
DNA Phenotyping: Snapshot of a Criminal.
Cell
; 166(5): 1061-1064, 2016 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27565333
3.
A high-performance neuroprosthesis for speech decoding and avatar control.
Nature
; 620(7976): 1037-1046, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612505
4.
An interactive atlas of three-dimensional syndromic facial morphology.
Am J Hum Genet
; 111(1): 39-47, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38181734
5.
Individual differences in human gaze behavior generalize from faces to objects.
Proc Natl Acad Sci U S A
; 121(12): e2322149121, 2024 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38470925
6.
Dynamic brain communication underwriting face pareidolia.
Proc Natl Acad Sci U S A
; 121(16): e2401196121, 2024 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38588422
7.
Accurate estimation of biological age and its application in disease prediction using a multimodal image Transformer system.
Proc Natl Acad Sci U S A
; 121(3): e2308812120, 2024 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38190540
8.
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Am J Hum Genet
; 110(2): 215-227, 2023 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36586412
9.
DNMT3B PWWP mutations cause hypermethylation of heterochromatin.
EMBO Rep
; 25(3): 1130-1155, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38291337
10.
PHF6-mediated transcriptional control of NSC via Ephrin receptors is impaired in the intellectual disability syndrome BFLS.
EMBO Rep
; 25(3): 1256-1281, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38429579
11.
Behavioral signatures of face perception emerge in deep neural networks optimized for face recognition.
Proc Natl Acad Sci U S A
; 120(32): e2220642120, 2023 08 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37523537
12.
Re-cognizing the new self: The neurocognitive plasticity of self-processing following facial transplantation.
Proc Natl Acad Sci U S A
; 120(14): e2211966120, 2023 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36972456
13.
Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation.
Hum Mol Genet
; 32(9): 1439-1456, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36458887
14.
An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome.
Am J Hum Genet
; 109(10): 1867-1884, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36130591
15.
Single-cell transcriptomic signatures and gene regulatory networks modulated by Wls in mammalian midline facial formation and clefts.
Development
; 149(14)2022 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35781558
16.
A 3.8-million-year-old hominin cranium from Woranso-Mille, Ethiopia.
Nature
; 573(7773): 214-219, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31462770
17.
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome.
J Med Genet
; 61(5): 490-501, 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38296633
18.
Eye drift during fixation predicts visual acuity.
Proc Natl Acad Sci U S A
; 119(49): e2200256119, 2022 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36442088
19.
Deep models of superficial face judgments.
Proc Natl Acad Sci U S A
; 119(17): e2115228119, 2022 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35446619
20.
Illusory faces are more likely to be perceived as male than female.
Proc Natl Acad Sci U S A
; 119(5)2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35074880