Miguel J. Xavier, BSc (Hon), MSc, PhD
Miguel J. Xavier, BSc (Hon), MSc, PhD
Institute of Genetic Medicine, Newcastle University
Bestätigte E-Mail-Adresse bei newcastle.ac.uk
Titel
Zitiert von
Zitiert von
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Transgenerational inheritance: how impacts to the epigenetic and genetic information of parents affect offspring health
MJ Xavier, SD Roman, RJ Aitken, B Nixon
Human reproduction update 25 (5), 519-541, 2019
742019
The Rho-family GTPase Rac1 regulates integrin localization in Drosophila immunosurveillance cells
MJ Xavier, MJ Williams
PLoS One 6 (5), e19504, 2011
342011
A directed miniscreen for genes involved in the Drosophila anti-parasitoid immune response
L Howell, CJ Sampson, MJ Xavier, E Bolukbasi, MMS Heck, MJ Williams
Immunogenetics 64 (2), 155-161, 2012
332012
Genome-wide analysis shows association of epigenetic changes in regulators of Rab and Rho GTPases with spinal muscular atrophy severity
GY Zheleznyakova, S Voisin, AV Kiselev, MS Almén, MJ Xavier, ...
European Journal of Human Genetics 21 (9), 988-993, 2013
282013
Disease gene discovery in male infertility: past, present and future
MJ Xavier, A Salas-Huetos, MS Oud, KI Aston, JA Veltman
Human Genetics 140 (1), 7-19, 2021
242021
Paternal impacts on development: identification of genomic regions vulnerable to oxidative DNA damage in human spermatozoa
MJ Xavier, B Nixon, SD Roman, RJ Scott, JR Drevet, RJ Aitken
Human Reproduction 34 (10), 1876-1890, 2019
232019
Bi-allelic mutations in M1AP are a frequent cause of meiotic arrest and severely impaired spermatogenesis leading to male infertility
MJ Wyrwoll, ŞG Temel, L Nagirnaja, MS Oud, AM Lopes, ...
The American Journal of Human Genetics 107 (2), 342-351, 2020
152020
Improved methods of DNA extraction from human spermatozoa that mitigate experimentally-induced oxidative DNA damage.
MJ Xavier, B Nixon, SD Roman, RJ Aitken
PloS One 13 (3), 2018
52018
A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships
BJ Houston, A Riera, MJ Wyrwoll, A Salas-Huetos, MJ Xavier, L Nagirnaja, ...
medRxiv, 2021
42021
The small non-coding RNA profile of mouse oocytes is modified during aging
BP Mihalas, NJ Camlin, MJ Xavier, AE Peters, JE Holt, JM Sutherland, ...
Aging (Albany NY) 11 (10), 2968, 2019
42019
Genomic integrity in the male germ line: evidence in support of the disposable soma hypothesis
MJ Xavier, LA Mitchell, KE McEwan, RJ Scott, RJ Aitken
Reproduction 156 (3), 269-282, 2018
32018
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure
JJ Hardy, MJ Wyrwoll, W Mcfadden, A Malcher, N Rotte, NC Pollock, ...
Human genetics, 1-14, 2021
22021
A de novo paradigm for male infertility
MS Oud, RM Smits, HE Smith, FK Mastrorosa, GS Holt, BJ Houston, ...
Nature Communications 13 (1), 1-10, 2022
2022
Acrylamide modulates the mouse epididymal proteome to drive alterations in the sperm small non-coding RNA profile and dysregulate embryo development
NA Trigg, DA Skerrett-Byrne, MJ Xavier, W Zhou, AL Anderson, ...
Cell Reports 37 (1), 109787, 2021
2021
A de novo paradigm for male infertility
J Veltman, M Oud, R Smits, H Smith, F Mastrorosa, G Holt, B Houston, ...
2021
Maternally inherited copy-number variations may explain cases of severe idiopathic male infertility
FK Mastrorosa, MJ Xavier, A Mikulasova, MS Oud, RM Smith, G Astuti, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 157-157, 2020
2020
Interrogating the parental and zygotic origin of de novo mutations in severe male infertility using long read sequencing
GS Holt, B Alobaidi, L Batty, M Oud, H Smith, P de Vries, R Smits, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 165-165, 2020
2020
Optimising long-range PCR methodology and long-read DNA sequencing
LE Batty, B Alobaidi, GS Holt, MS Oud, HE Smith, PF de Vries, RM Smits, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 602-603, 2020
2020
Biallelic mutations in M1AP are associated with meiotic arrest, severely impaired spermatogenesis and male infertility
C Friedrich, SG Temel, L Nagirnaja, MS Oud, AM Lopes, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 1002-1003, 2020
2020
Further indication of a role for de novo mutations in cases of severe idiopathic male infertility
HE Smith, MS Oud, PF de Vries, B Alobaidi, A Virdi, BJ Houston, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 155-155, 2020
2020
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