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TITLE: Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility  Full Text
AUTHORS: Daniela Felício; Andreia Dias; Sandra Martins ; Estefânia Carvalho; Alexandra Lopes; Nádia Pinto ; Carolina Lemos; Mariana Santos; Miguel Alves Ferreira;
PUBLISHED: 2023, SOURCE: Journal of Headache and Pain, VOLUME: 24, ISSUE: 1
INDEXED IN: Scopus CrossRef
12
TITLE: RAMP1 PROMOTER METHYLATION STATUS IN PORTUGUESE AND SPANISH WOMEN WITH MIGRAINE  Full Text
AUTHORS: Carvalho, Estefania; Dias, Andreia; Guerrero, Angel L.; Gomez, Carlos; Sousa, Alda; Lopes, Alexandra M.; Martins, Sandra; Pinto, Nadia ; Lemos, Carolina; Alves Ferreira, Miguel;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
13
TITLE: The sequence of the repetitive motif influences the frequency of multistep mutations in Short Tandem Repeats  Full Text
AUTHORS: Antao Sousa, Sofia; Pinto, Nadia ; Rende, Pablo; Amorim, Antonio ; Gusmao, Leonor;
PUBLISHED: 2023, SOURCE: SCIENTIFIC REPORTS, VOLUME: 13, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 1
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TITLE: A High Methylation Level of a Novel -284 bp CpG Island in the RAMP1 Gene Promoter Is Potentially Associated with Migraine in Women  Full Text
AUTHORS: Carvalho, Estefania; Dias, Andreia; Sousa, Alda; Lopes, Alexandra M. ; Martins, Sandra ; Pinto, Nadia ; Lemos, Carolina; Alves Ferreira, Miguel;
PUBLISHED: 2022, SOURCE: BRAIN SCIENCES, VOLUME: 12, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 1
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TITLE: EPIGENETIC ANALYSIS OF THE CGRP PATHWAY GENES INVOLVED IN MIGRAINE  Full Text
AUTHORS: Carvalho, Estefania; Dias, Andreia; Sousa, Alda; Sequeiros, Jorge; Lopes, Alexandra; Martins, Sandra; Pinto, Nadia ; Lemos, Carolina; Alves Ferreira, Miguel;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
17
TITLE: Haplodiploid Markers and Their Forensic Relevance
AUTHORS: Antonio Amorim; Nadia Pinto ;
PUBLISHED: 2022, SOURCE: Handbook of DNA Profiling
INDEXED IN: CrossRef: 1
18
TITLE: How frequently are Autosomal and X-STRs multistep mutations perceived as single-step?  Full Text
AUTHORS: Antao Sousa, Sofia; Conde Sousa, Eduardo; Gusmao, Leonor; Amorim, Antonio ; Pinto, Nadia ;
PUBLISHED: 2022, SOURCE: FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 1 Unpaywall
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TITLE: How often have X- and autosomal-STRs mutations equivocal parental origin been assigned?  Full Text
AUTHORS: Antao Sousa, Sofia; Sousa, Eduardo Conde; Gusmao, Leonor; Amorim, Antonio ; Pinto, Nadia ;
PUBLISHED: 2022, SOURCE: FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES, VOLUME: 8
INDEXED IN: Scopus WOS CrossRef: 1 Unpaywall
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TITLE: Paternal half-sisters or unrelated-How can the X-chromosomal evidence be quantified when one female presents trisomy X?  Full Text
AUTHORS: Faustino, Marisa; Turchi, Chiara; Kling, Daniel; Gusmao, Leonor; Amorim, Antonio ; Pinto, Nadia ;
PUBLISHED: 2022, SOURCE: FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES, VOLUME: 8, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef Unpaywall
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