Heterogeneity of Brain Dynamics in Genetic and Psychiatric Conditions
Adrien E. E. Dubois, Sarah Lippé, Charles-Olivier Martin, Inga Sophia Knoth et autres
0 citationsbioRxiv (Cold Spring Harbor Laboratory)
Melissa T. Carter
Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.
76Publications signalées
5465Citations signalées
2Affiliations récentes
Institutions déclarées
Domaines associés
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental DisordersGenomics and Rare DiseasesAutism Spectrum Disorder ResearchCongenital heart defects research
Publications récentes
Adult‐Onset CTC1 ‐Related Disorder With Kidney Disease, Subcutaneous Dystrophic Calcifications and Telomere Length Conservation
Élisabeth Soubry, Julianne K. Postma, Meredith Gillespie, Yoko Ito et autres
0 citationsAmerican Journal of Medical Genetics Part A
The Patient-reported Genetic testing Utility InDEx: A novel measure of personal utility
Elise Poole, Bowen Xiao, Stephanie Luca, Daniel Assamad et autres
0 citationsGenetics in Medicine
The Q1K Integrated EEG and Eye-Tracking Experimental Test Battery for Open Autism Science
Christian O’Reilly, James Desjardins, Gabriel Blanco-Gomez, Scott Huberty et autres
1 citationbioRxiv (Cold Spring Harbor Laboratory)
The Q1K Integrated EEG and Eye-Tracking Experimental Test Battery - Experiment Builder Task Scripts
Christian O’Reilly, James Desjardins, Gabriel Blanco-Gomez, Scott Huberty et autres
0 citationsZenodo (CERN European Organization for Nuclear Research)
The Q1K Integrated EEG and Eye-Tracking Experimental Test Battery - Experiment Builder Task Scripts
Christian O’Reilly, James Desjardins, Gabriel Blanco-Gomez, Scott Huberty et autres
0 citationsZenodo (CERN European Organization for Nuclear Research)
Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder
Kazuyuki Komatsu, Atsushi Sugie, Yohei Nitta, Jiro Osaka et autres
1 citationEuropean Journal of Human Genetics
De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder
Samuel M Bradbrook, Gail E. Graham, Melissa T. Carter, Maria Kibæk et autres
1 citationAmerican Journal of Medical Genetics Part A
Congenital-onset MLASA2 from a novel YARS2 variant: A literature review
Astrid Eisenkölbl, Hanns Lochmüller, Melissa T. Carter, Leslie E. Hamilton et autres
2 citationsJournal of Neuromuscular Diseases
Corticosteroid-binding Globulin Dysfunction Due to Homozygous SERPINA6 Lyon Variant in a Pediatric Patient
Mary Jiang, Caroline Zuijdwijk, Melissa T. Carter, Alexandra Ahmet
0 citationsJCEM Case Reports
Familial inheritance of 14q terminal deletion syndrome and review of the literature
Krista M. Vincent, Bradley Prince, McGowan-Jordan Jean, Melissa T. Carter
1 citationEuropean Journal of Medical Genetics
25 Genomic medicine in paediatric care for neurodevelopmental disorders: An assessment of practices, attitudes and education needs of Ontario paediatricians
Anna Szuto, Megan F. Dickson, Danielle Baribeau, June Carroll et autres
0 citationsPaediatrics & Child Health
BNTIC News n’est pas le producteur de ces données. Recherche à la demande dans Crossref et Europe PMC, sans clé ; OpenAlex reste optionnel. Aucun service payant requis, aucune réponse conservée. Sources et limites.