Suchergebnisse - "Lewis, M E"

PubPharm (260)

1

Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant

enthalten in: Genes | 2023

von Yip, S. | Calli, K. | Qiao, Y. | +3

2

Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von van Jaarsveld, R. | Reilly, J. | Cornips, M. | +56

3

Genomic architecture of autism from comprehensive whole-genome sequence annotation

enthalten in: Cell | 2022

von Trost, B. | Thiruvahindrapuram, B. | Chan, A. | +98

4

The potential for over diagnosis of Paget's disease of bone using macroscopic analysis

enthalten in: International journal of paleopathology | 2022

von Garnett, E. | Lewis, M.

5

Genomic architecture of Autism Spectrum Disorder from comprehensive whole-genome sequence annotation

enthalten in: bioRxiv.org | 2022

von Trost, B. | Thiruvahindrapuram, B. | Chan, A. | +101

6

Tackling healthcare access barriers for individuals with autism from diagnosis to adulthood

enthalten in: Pediatric research | 2022

von Malik-Soni, N. | Shaker, A. | Luck, H. | +5

CommentIn: Pediatr Res. 2022 Apr;91(5):1025-1027. - PMID 34108624

7

Complex Autism Spectrum Disorder with Epilepsy, Strabismus and Self-Injurious Behaviors in a Patient with a De Novo Heterozygous POLR2A Variant

enthalten in: Genes | 2022

von Evans, D. | Qiao, Y. | Trost, B. | +5

8

Highly prevalent Russian HIV-1 V3-loop sequence variants are susceptible to maraviroc

enthalten in: Antiviral chemistry & chemotherapy | 2021

von Lewis, M. | Jubb, B. | Simpson, P. | +7

9

V3-Loop genotypes do not predict maraviroc susceptibility of CCR5-tropic virus or clinical response through week 48 in HIV-1-infected, treatment-experienced persons receiving optimized background regimens

enthalten in: Antiviral chemistry & chemotherapy | 2021

von Lewis, M. | Simpson, P. | Mori, J. | +7

10

Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome

enthalten in: American journal of medical genetics. Part A | 2021

von Dyment, D. | O'Donnell-Luria, A. | Agrawal, P. | +73

1
2
3
4
5
6
7
8
9
10
11
Nächster »
[26]