These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
186 related articles for article (PubMed ID: 39167997)
1. Emerging X-linked genes associated with neurodevelopmental disorders in females. Lukin J; Smith CM; De Rubeis S Curr Opin Neurobiol; 2024 Oct; 88():102902. PubMed ID: 39167997 [TBL] [Abstract][Full Text] [Related]
2. Pathogenic paternally inherited NLGN4X deletion in a female with autism spectrum disorder: Clinical, cytogenetic, and molecular characterization. Kopp N; Amarillo I; Martinez-Agosto J; Quintero-Rivera F Am J Med Genet A; 2021 Mar; 185(3):894-900. PubMed ID: 33369065 [TBL] [Abstract][Full Text] [Related]
3. Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders. Prem S; Millonig JH; DiCicco-Bloom E Adv Neurobiol; 2020; 25():109-153. PubMed ID: 32578146 [TBL] [Abstract][Full Text] [Related]
4. Targeted sequencing and integrative analysis of 3,195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes. Wang T; Zhang Y; Liu L; Wang Y; Chen H; Fan T; Li J; Xia K; Sun Z J Genet Genomics; 2021 Apr; 48(4):312-323. PubMed ID: 33994118 [TBL] [Abstract][Full Text] [Related]
5. Annual research review: The (epi)genetics of neurodevelopmental disorders in the era of whole-genome sequencing--unveiling the dark matter. Kiser DP; Rivero O; Lesch KP J Child Psychol Psychiatry; 2015 Mar; 56(3):278-95. PubMed ID: 25677560 [TBL] [Abstract][Full Text] [Related]
6. Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk. McKenna B; Koomar T; Vervier K; Kremsreiter J; Michaelson JJ Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30559312 [TBL] [Abstract][Full Text] [Related]
7. Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort. Chen S; Xiong J; Chen B; Zhang C; Deng X; He F; Yang L; Chen C; Peng J; Yin F Clin Chim Acta; 2022 Jan; 524():179-186. PubMed ID: 34800434 [TBL] [Abstract][Full Text] [Related]
8. Dosage Compensation in Females with X-Linked Metabolic Disorders. Juchniewicz P; Piotrowska E; Kloska A; Podlacha M; Mantej J; Węgrzyn G; Tukaj S; Jakóbkiewicz-Banecka J Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33925963 [TBL] [Abstract][Full Text] [Related]
10. High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders. Spataro N; Trujillo-Quintero JP; Manso C; Gabau E; Capdevila N; Martinez-Glez V; Berenguer-Llergo A; Reyes S; Brunet A; Baena N; Guitart M; Ruiz A Genes (Basel); 2023 Mar; 14(3):. PubMed ID: 36980980 [TBL] [Abstract][Full Text] [Related]
11. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders. Nguyen HT; Bryois J; Kim A; Dobbyn A; Huckins LM; Munoz-Manchado AB; Ruderfer DM; Genovese G; Fromer M; Xu X; Pinto D; Linnarsson S; Verhage M; Smit AB; Hjerling-Leffler J; Buxbaum JD; Hultman C; Sklar P; Purcell SM; Lage K; He X; Sullivan PF; Stahl EA Genome Med; 2017 Dec; 9(1):114. PubMed ID: 29262854 [TBL] [Abstract][Full Text] [Related]
12. Why females are mosaics, X-chromosome inactivation, and sex differences in disease. Migeon BR Gend Med; 2007 Jun; 4(2):97-105. PubMed ID: 17707844 [TBL] [Abstract][Full Text] [Related]
13. The pathogenicity of genomic/genetic variant of X-chromosomal genes in males with intellectual disability. Peng JP; Liu F; Xie H; Chen XL Yi Chuan; 2017 Jun; 39(6):455-468. PubMed ID: 28903905 [TBL] [Abstract][Full Text] [Related]
14. The contribution of X-linked coding variation to severe developmental disorders. Martin HC; Gardner EJ; Samocha KE; Kaplanis J; Akawi N; Sifrim A; Eberhardt RY; Tavares ALT; Neville MDC; Niemi MEK; Gallone G; McRae J; ; Wright CF; FitzPatrick DR; Firth HV; Hurles ME Nat Commun; 2021 Jan; 12(1):627. PubMed ID: 33504798 [TBL] [Abstract][Full Text] [Related]
15. Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders. Pang N; Li K; Tan S; Chen M; He F; Chen C; Yang L; Zhang C; Deng X; Yang L; Mao L; Wang G; Duan H; Wang X; Zhang W; Guo H; Peng J; Yin F; Xia K Gene; 2024 Mar; 897():148071. PubMed ID: 38081334 [TBL] [Abstract][Full Text] [Related]
16. Association of maternal diabetes with neurodevelopmental disorders: autism spectrum disorders, attention-deficit/hyperactivity disorder and intellectual disability. Chen S; Zhao S; Dalman C; Karlsson H; Gardner R Int J Epidemiol; 2021 May; 50(2):459-474. PubMed ID: 33221916 [TBL] [Abstract][Full Text] [Related]
17. Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders. Arnett AB; Wang T; Eichler EE; Bernier RA J Neurodev Disord; 2021 Jun; 13(1):24. PubMed ID: 34148555 [TBL] [Abstract][Full Text] [Related]
18. Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders. Turner TN; Wilfert AB; Bakken TE; Bernier RA; Pepper MR; Zhang Z; Torene RI; Retterer K; Eichler EE Am J Hum Genet; 2019 Dec; 105(6):1274-1285. PubMed ID: 31785789 [TBL] [Abstract][Full Text] [Related]
19. Genes that escape from X-chromosome inactivation: Potential contributors to Klinefelter syndrome. Navarro-Cobos MJ; Balaton BP; Brown CJ Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):226-238. PubMed ID: 32441398 [TBL] [Abstract][Full Text] [Related]