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TITLE: A de novo paradigm for male infertility
AUTHORS: Oud M.S.; Smits R.M.; Smith H.E.; Mastrorosa F.K.; Holt G.S.; Houston B.J.; de Vries P.F.; Alobaidi B.K.S.; Batty L.E.; Ismail H.; Greenwood J.; Sheth H.; Mikulasova A.; Astuti G.D.N.; Gilissen C.; McEleny K.; Turner H.; Coxhead J.; Cockell S.; Braat D.D.M.; Fleischer K.; D’Hauwers K.W.M.; Schaafsma E.; Donald F Conrad; Douglas T Carrell; James M Hotaling; Timothy G Jenkins; Rob McLachlan; Moira K O’Bryan; Moira K O’Bryan; Peter N Schlegel; Michael L Eisenberg; Jay I Sandlow; Emily S Jungheim; Kenan R Omurtag; Alexandra M Lopes ; Susana Seixas; Filipa Carvalho ; Susana Fernandes; Alberto Barros ; João Gonçalves; Iris Caetano; Graça Pinto; Sónia Correia; Maris Laan; Margus Punab; Ewa Rajpert De Meyts; Niels Jørgensen; Kristian Almstrup; Csilla G Krausz; Keith A Jarvi; Nagirnaja L.; Nagirnaja L.; Conrad D.F.; Friedrich C.; Kliesch S.; Aston K.I.; Aston K.I.; Riera-Escamilla A.; Krausz C.; Gonzaga-Jauregui C.; Santibanez-Koref M.; Elliott D.J.; Vissers L.E.L.M.; Tüttelmann F.; Ramos L.; Xavier M.J.; van der Heijden G.W.; Veltman J.A.; ...More
PUBLISHED: 2022, SOURCE: NATURE COMMUNICATIONS, VOLUME: 13, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 50
2
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
3
TITLE: Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management
AUTHORS: Kasak, Laura; Lillepea, Kristiina; Nagirnaja, Liina; Aston, Kenneth, I; Schlegel, Peter N.; Goncalves, Joao; Carvalho, Filipa ; Moreno Mendoza, Daniel; Almstrup, Kristian; Eisenberg, Michael L.; Jarvi, Keith A.; O'Bryan, Moira K.; Lopes, Alexandra M. ; Conrad, Donald F.; Punab, Margus; Laan, Maris;
PUBLISHED: 2022, SOURCE: HUMAN REPRODUCTION, VOLUME: 37, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 5 Unpaywall
4
TITLE: Clinical and genetic characterization of seven Portuguese patients with KMT2B variants
AUTHORS: Lopes, Alexandra M. ; Sousa, Susana; Lopes, Ana; Silva, Paulo; Morais, Sara; Brandao, Ana F.; Lopes, Fatima; Bastos Ferreira, Rita; Jorge, Andre; Januario, Cristina; Costa, Henrique M.; Bras, Ana C.; Quental, Rita; Leao, Miguel; Damasio, Joana; Magalhaes, Marina; Freixo, Joao P.; Sequeiros, Jorge; Oliveira, Jorge;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
5
TITLE: Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility  Full Text
AUTHORS: Cervan Martin, Miriam; Bossini Castillo, Lara; Guzman Jimenez, Andrea; Rivera Egea, Rocio; Garrido, Nicolas; Lujan, Saturnino; Romeu, Gema; Santos Ribeiro, Samuel; Antonio Castilla, Jose; del Carmen Gonzalvo, Maria; Clavero, Ana; Maldonado, Vicente; Javier Vicente, Francisco; Burgos, Miguel; Jimenez, Rafael; Gonzalez Munoz, Sara; Sanchez Curbelo, Josvany; Lopez Rodrigo, Olga; Pereira Caetano, Iris; Marques, Patricia Isabel; Carvalho, Filipa ; Barros, Alberto ; Bassas, Lluis; Seixas, Susana; Goncalves, Joao; Larriba, Sara; Lopes, Alexandra Manuel ; Jesus Palomino Morales, Rogelio; David Carmona, Francisco; ...More
PUBLISHED: 2022, SOURCE: ANDROLOGY, VOLUME: 10, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 4 Unpaywall
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TITLE: Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome
AUTHORS: Cervan Martin, Miriam; Bossini Castillo, Lara; Guzman Jimenez, Andrea; Rivera Egea, Rocio; Garrido, Nicolas; Lujan, Saturnino; Romeu, Gema; Santos Ribeiro, Samuel; Castilla, Jose A.; Gonzalvo, M. Carmen; Clavero, Ana; Vicente, F. Javier; Maldonado, Vicente; Gonzalez Munoz, Sara; Rodriguez Martin, Inmaculada; Burgos, Miguel; Jimenez, Rafael; Pinto, Maria Graca; Pereira, Isabel; Nunes, Joaquim; Sanchez Curbelo, Josvany; Lopez Rodrigo, Olga; Pereira Caetano, Iris; Marques, Patricia Isabel; Carvalho, Filipa ; Barros, Alberto ; Bassas, Lluis; Seixas, Susana; Goncalves, Joao; Larriba, Sara; Lopes, Alexandra M. ; Carmona, F. David; Palomino Morales, Rogelio J.; ...More
PUBLISHED: 2022, SOURCE: JOURNAL OF PERSONALIZED MEDICINE, VOLUME: 12, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef Unpaywall
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TITLE: Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
AUTHORS: Guzmán Jiménez, A; González Muñoz, S; Cerván Martín, M; Rivera Egea, R; Garrido, N; Luján, S; Santos Ribeiro, S; Castilla, JA; Gonzalvo, MC; Clavero, A; Vicente, FJ; Maldonado, V; Villegas Salmerón, J; Burgos, M; Jiménez, R; Pinto, MG; Pereira, I; Nunes, J; Sánchez Curbelo, J; López Rodrigo, O; Pereira Caetano, I; Marques, PI; Carvalho, F ; Barros, A ; Bassas, L; Seixas, S; Gonçalves, J; Lopes, AM ; Larriba, S; Palomino Morales, RJ; Carmona, FD; Bossini Castillo, L; Group IVIRMA; Clinical Group Lisbon; ...More
PUBLISHED: 2022, SOURCE: FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, VOLUME: 10
INDEXED IN: Scopus WOS CrossRef: 1 Unpaywall
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TITLE: Copy number variants in a large cohort analysed with whole-exome sequencing: lessons for genetic diagnosis
AUTHORS: Lopes, Fatima; Lopes, Alexandra M. ; Silva, Paulo; Sousa, Susana; Morais, Sara; Sa, Joana; Brandao, Ana Filipa; Lopes, Ana; Bastos Ferreira, Rita; Freixo, Joao Parente; Sequeiros, Jorge; Oliveira, Jorge;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
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TITLE: DDB1-and CUL4-associated factor 12-like protein 1 (Dcaf12l1) is not essential for male fertility in mice
AUTHORS: Houston, Brendan J.; Lopes, Alexandra M. ; Laan, Maris; Nagirnaja, Liina; O'Connor, Anne E.; Merriner, D. Jo; Nguyen, Joseph; Punab, Margus; Riera Escamilla, Antoni; Krausz, Csilla; Aston, Kenneth Ivan; Conrad, Donald F.; O'Bryan, Moira K.;
PUBLISHED: 2022, SOURCE: DEVELOPMENTAL BIOLOGY, VOLUME: 490
INDEXED IN: Scopus WOS
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TITLE: Diverse monogenic subforms of human spermatogenic failure
AUTHORS: Nagirnaja, Liina; Lopes, Alexandra M. ; Charng, Wu Lin; Miller, Brian; Stakaitis, Rytis; Golubickaite, Ieva; Stendahl, Alexandra; Luan, Tianpengcheng; Friedrich, Corinna; Mahyari, Eisa; Fadial, Eloise; Kasak, Laura; Vigh Conrad, Katinka; Oud, Manon S.; Xavier, Miguel J.; Cheers, Samuel R.; James, Emma R.; Guo, Jingtao; Jenkins, Timothy G.; Riera Escamilla, Antoni; Barros, Alberto; Carvalho, Filipa ; Fernandes, Susana; Goncalves, Joao; Gurnett, Christina A.; Jorgensen, Niels; Jezek, Davor; Jungheim, Emily S.; Kliesch, Sabine; McLachlan, Robert, I; Omurtag, Kenan R.; Pilatz, Adrian; Sandlow, Jay; Smith, James; Eisenberg, Michael L.; Hotaling, James M.; Jarvi, Keith A.; Punab, Margus; Rajpert De Meyts, Ewa; Carrell, Douglas T.; Krausz, Csilla; Laan, Maris; O'Bryan, Moira K.; Schlegel, Peter N.; Tuettelmann, Frank; Veltman, Joris A.; Almstrup, Kristian; Aston, Kenneth, I; Conrad, Donald F.; ...More
PUBLISHED: 2022, SOURCE: NATURE COMMUNICATIONS, VOLUME: 13, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 34 Unpaywall
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