Alexandra M. Lopes researcher
Lopes, Alexandra Manuel Ferreira
VIAF ID: 99051529 (Personal)
Permalink: http://viaf.org/viaf/99051529
Preferred Forms
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Works
Title | Sources |
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The 8p23 inversion polymorphism determines local recombination heterogeneity across human populations | |
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia | |
Bimodal allele frequency distribution at Y-STR loci DYS392 and DYS438: no evidence for a deviation from the stepwise mutation model | |
Clustered transcripts that escape X inactivation at mouse XqD. | |
Distinctive patterns of evolution of the δ-globin gene (HBD) in primates | |
Evaluating the Neolithic Expansion at Both Shores of the Mediterranean Sea. | |
Evolutionary constraints in the β-globin cluster: the signature of purifying selection at the δ-globin (HBD) locus and its role in developmental gene regulation | |
Exploring the regulatory networks of spermatogenesis from candidate gene approaches to integrative functional genomics | |
Forensic genetics and genomics: Much more than just a human affair | |
Genetic diversity within two Tunisian wild jirds: Meriones shawi and Meriones libycus (Rodentia, Gerbillinae) | |
Grouping of Y-STR haplotypes discloses European geographic clines. | |
The human RPS4 paralogue on Yq11.223 encodes a structurally conserved ribosomal protein and is preferentially expressed during spermatogenesis | |
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. | |
Inactivation status of PCDH11X: sexual dimorphisms in gene expression levels in brain | |
Methylation of two Homo sapiens-specific X-Y homologous genes in Klinefelter's syndrome (XXY). | |
Micro-phylogeographic and demographic history of Portuguese male lineages | |
Microsatellite Variation and Evolutionary History of PCDHX/Y Gene Pair Within the Xq21.3/Yp11.2 Hominid-Specific Homology Block | |
Multispecies Purification of Testicular Germ Cells | |
The mutational spectrum of WT1 in male infertility. | |
A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia | |
On the structural plasticity of the human genome: chromosomal inversions revisited | |
Rare double sex and mab-3-related transcription factor 1 regulatory variants in severe spermatogenic failure | |
Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism | |
Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula. | |
Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome |