Hayley S Mountford[Author] - Search Results

Year	Number of Results
2011	1
2013	1
2014	1
2015	1
2017	2
2018	1
2019	1
2020	4
2021	2
2022	2
2023	1
2024	2
2025	3
2026	0

1

Genetic neurodevelopmental clustering and dyslexia.

Ciulkinyte A, Mountford HS, Fontanillas P; 23andMe Research Team; Bates TC, Martin NG, Fisher SE, Luciano M. Ciulkinyte A, et al. Among authors: mountford hs. Mol Psychiatry. 2025 Jan;30(1):140-150. doi: 10.1038/s41380-024-02649-8. Epub 2024 Jul 15. Mol Psychiatry. 2025. PMID: 39009701 Free PMC article.

2

Genome-Wide Association Study of Motor Coordination.

Mountford HS, Hill A, Barnett AL, Newbury DF. Mountford HS, et al. Front Hum Neurosci. 2021 Jun 9;15:669902. doi: 10.3389/fnhum.2021.669902. eCollection 2021. Front Hum Neurosci. 2021. PMID: 34177493 Free PMC article.

3

Corrigendum: Genome-wide association study of motor coordination.

Mountford HS, Hill A, Barnett AL, Newbury DF. Mountford HS, et al. Front Hum Neurosci. 2024 Jan 23;18:1360116. doi: 10.3389/fnhum.2024.1360116. eCollection 2024. Front Hum Neurosci. 2024. PMID: 38322780 Free PMC article.

4

The Genetic and Molecular Basis of Developmental Language Disorder: A Review.

Mountford HS, Braden R, Newbury DF, Morgan AT. Mountford HS, et al. Children (Basel). 2022 Apr 20;9(5):586. doi: 10.3390/children9050586. Children (Basel). 2022. PMID: 35626763 Free PMC article. Review.

5

A family study implicates GBE1 in the etiology of autism spectrum disorder.

Fanjul-Fernández M, Brown NJ, Hickey P, Diakumis P, Rafehi H, Bozaoglu K, Green CC, Rattray A, Young S, Alhuzaimi D, Mountford HS, Gillies G, Lukic V, Vick T, Finlay K, Coe BP, Eichler EE, Delatycki MB, Wilson SJ, Bahlo M, Scheffer IE, Lockhart PJ. Fanjul-Fernández M, et al. Among authors: mountford hs. Hum Mutat. 2022 Jan;43(1):16-29. doi: 10.1002/humu.24289. Epub 2021 Oct 21. Hum Mutat. 2022. PMID: 34633740 Free PMC article.

6

Longitudinal Reading Measures and Genome Imputation in the National Child Development Study: Prospects for Future Reading Research.

Bridges EC, Rayner NW, Mountford HS, Bates TC, Luciano M. Bridges EC, et al. Among authors: mountford hs. Twin Res Hum Genet. 2023 Feb;26(1):10-20. doi: 10.1017/thg.2023.2. Epub 2023 Mar 10. Twin Res Hum Genet. 2023. PMID: 36896826

7

HIGD2A is Required for Assembly of the COX3 Module of Human Mitochondrial Complex IV.

Hock DH, Reljic B, Ang CS, Muellner-Wong L, Mountford HS, Compton AG, Ryan MT, Thorburn DR, Stroud DA. Hock DH, et al. Among authors: mountford hs. Mol Cell Proteomics. 2020 Jul;19(7):1145-1160. doi: 10.1074/mcp.RA120.002076. Epub 2020 Apr 21. Mol Cell Proteomics. 2020. PMID: 32317297 Free PMC article.

8

Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes.

Perrino PA, Talbot L, Kirkland R, Hill A, Rendall AR, Mountford HS, Taylor J; WGS500 Consortium; Buscarello AN, Lahiri N, Saggar A, Fitch RH, Newbury DF. Perrino PA, et al. Among authors: mountford hs. Commun Biol. 2020 Apr 20;3(1):180. doi: 10.1038/s42003-020-0885-5. Commun Biol. 2020. PMID: 32313182 Free PMC article.

9

Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature review.

Mordaunt DA, Jolley A, Balasubramaniam S, Thorburn DR, Mountford HS, Compton AG, Nicholl J, Manton N, Clark D, Bratkovic D, Friend K, Yu S. Mordaunt DA, et al. Among authors: mountford hs. Am J Med Genet A. 2015 Jun;167(6):1330-6. doi: 10.1002/ajmg.a.36968. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25899669 Review.

10

Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.

Mountford HS, Bishop DVM, Thompson PA, Simpson NH, Newbury DF. Mountford HS, et al. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):256-266. doi: 10.1002/ajmg.c.31791. Epub 2020 May 26. Am J Med Genet C Semin Med Genet. 2020. PMID: 32452638

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