Manuel Carlos Loureiro de Lemos
AuthID: R-000-K5Y
1
TITLE: Germline genetic variants in young-onset sporadic pituitary macroadenomas: A multigene panel analysis
AUTHORS: Leonor Gaspar; Catarina Gonçalves; Ema Nobre; Fernando Fonseca; Cláudia Amaral; João Duarte; Luísa Raimundo; Catarina Saraiva; Luísa Cortez; Olinda Marques; Manuel Lemos;
PUBLISHED: 2025, SOURCE: JOURNAL OF CLINICAL AND TRANSLATIONAL ENDOCRINOLOGY, VOLUME: 40
AUTHORS: Leonor Gaspar; Catarina Gonçalves; Ema Nobre; Fernando Fonseca; Cláudia Amaral; João Duarte; Luísa Raimundo; Catarina Saraiva; Luísa Cortez; Olinda Marques; Manuel Lemos;
PUBLISHED: 2025, SOURCE: JOURNAL OF CLINICAL AND TRANSLATIONAL ENDOCRINOLOGY, VOLUME: 40
INDEXED IN: 
Scopus 
WOS
Scopus WOS2
TITLE: Computational Resources and Infrastructures for a Novel Bioinformatics Laboratory: A Case Study
AUTHORS: Maldonado, E. ; Lemos, Manuel C.;
PUBLISHED: 2025, SOURCE: TECHNOLOGIES, VOLUME: 13, ISSUE: 7
AUTHORS: Maldonado, E. ; Lemos, Manuel C.;
PUBLISHED: 2025, SOURCE: TECHNOLOGIES, VOLUME: 13, ISSUE: 7
3
TITLE: Genetics of GH Deficiency: Insights From a Cohort of 203 Patients
AUTHORS: Ribeiro, Ana Claudia; Coutinho, Eduarda; Syed, Najeeb; Bastos, Margarida; Bacelar, Conceicao; Costa, Carla; Freitas, Paula; Gomes, Leonor; Agapito, Ana; Fonseca, Fernando; Amaral, Daniela; Carvalho, Davide; Sampaio, Maria Lurdes; Pereira, Bernardo Dias; Antunes, Ana Maria; Leite, Valeriano; Castro, Joao Jacome; Barros, Luisa; Pina, Rosa; Martins, Sofia Almeida; ...More
PUBLISHED: 2025, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
AUTHORS: Ribeiro, Ana Claudia; Coutinho, Eduarda; Syed, Najeeb; Bastos, Margarida; Bacelar, Conceicao; Costa, Carla; Freitas, Paula; Gomes, Leonor; Agapito, Ana; Fonseca, Fernando; Amaral, Daniela; Carvalho, Davide; Sampaio, Maria Lurdes; Pereira, Bernardo Dias; Antunes, Ana Maria; Leite, Valeriano; Castro, Joao Jacome; Barros, Luisa; Pina, Rosa; Martins, Sofia Almeida; ...More
PUBLISHED: 2025, SOURCE: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
4
TITLE: Genetic architecture of congenital hypogonadotropic hypogonadism: insights from analysis of a Portuguese cohort
AUTHORS: Carrico, Josianne Nunes; Goncalves, Catarina Ines; Al Naama, Asma; Syed, Najeeb; Aragues, Jose Maria; Bastos, Margarida; Fonseca, Fernando; Borges, Teresa; Pereira, Bernardo Dias; Pignatelli, Duarte; Carvalho, Davide ; Cunha, Filipe; Saavedra, Ana; Rodrigues, Elisabete; Saraiva, Joana; Ruas, Luisa; Vicente, Nuno; Martins, Joao Martin; De Sousa Lages, Adriana; Oliveira, Maria Joao; ...More
PUBLISHED: 2024, SOURCE: HUMAN REPRODUCTION OPEN, VOLUME: 2024, ISSUE: 3
AUTHORS: Carrico, Josianne Nunes; Goncalves, Catarina Ines; Al Naama, Asma; Syed, Najeeb; Aragues, Jose Maria; Bastos, Margarida; Fonseca, Fernando; Borges, Teresa; Pereira, Bernardo Dias; Pignatelli, Duarte; Carvalho, Davide ; Cunha, Filipe; Saavedra, Ana; Rodrigues, Elisabete; Saraiva, Joana; Ruas, Luisa; Vicente, Nuno; Martins, Joao Martin; De Sousa Lages, Adriana; Oliveira, Maria Joao; ...More
PUBLISHED: 2024, SOURCE: HUMAN REPRODUCTION OPEN, VOLUME: 2024, ISSUE: 3
5
TITLE: Palmoplantar pustulosis; [Pustulose palmo-plantar]
AUTHORS: Inês Farinha; Joni Carvalho; Carlos Loureiro; Ana Todo Bom;
PUBLISHED: 2024, SOURCE: Revista Portuguesa de Imunoalergologia, VOLUME: 32, ISSUE: 2
AUTHORS: Inês Farinha; Joni Carvalho; Carlos Loureiro; Ana Todo Bom;
PUBLISHED: 2024, SOURCE: Revista Portuguesa de Imunoalergologia, VOLUME: 32, ISSUE: 2
INDEXED IN: Scopus
Scopus6
TITLE: Kallmann Syndrome: Functional Analysis of a CHD7 Missense Variant Shows Aberrant RNA Splicing Full Text
AUTHORS: Carrico, Josianne Nunes; Goncalves, Catarina Ines; Aragues, Jose Maria; Lemos, Manuel Carlos;
PUBLISHED: 2024, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 25, ISSUE: 22
AUTHORS: Carrico, Josianne Nunes; Goncalves, Catarina Ines; Aragues, Jose Maria; Lemos, Manuel Carlos;
PUBLISHED: 2024, SOURCE: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, VOLUME: 25, ISSUE: 22
7
TITLE: Growth Hormone deficiency: spectrum of causal genetic variants in Portuguese patients
AUTHORS: Ribeiro, Ana C.; Syed, Najeeb; Saraiva, Luis R.; Lemos, Manuel C.;
PUBLISHED: 2024, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 32
AUTHORS: Ribeiro, Ana C.; Syed, Najeeb; Saraiva, Luis R.; Lemos, Manuel C.;
PUBLISHED: 2024, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 32
INDEXED IN: WOS
WOS8
TITLE: Regulation of ABC transporters by sex steroids may explain differences in drug resistance between sexes
AUTHORS: Mineiro, Rafael; Santos, Cecilia; Goncalves, Isabel; Lemos, Manuel; Cavaco, Jose Eduardo B.; Quintela, Telma;
PUBLISHED: 2023, SOURCE: JOURNAL OF PHYSIOLOGY AND BIOCHEMISTRY, VOLUME: 79, ISSUE: 3
AUTHORS: Mineiro, Rafael; Santos, Cecilia; Goncalves, Isabel; Lemos, Manuel; Cavaco, Jose Eduardo B.; Quintela, Telma;
PUBLISHED: 2023, SOURCE: JOURNAL OF PHYSIOLOGY AND BIOCHEMISTRY, VOLUME: 79, ISSUE: 3
9
TITLE: Low frequency of AIP mutations in patients with young-onset sporadic pituitary macroadenomas
AUTHORS: Gaspar, L. M.; Goncalves, C. I.; Saraiva, C.; Cortez, L.; Amaral, C.; Nobre, E.; Lemos, M. C.;
PUBLISHED: 2023, SOURCE: JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, VOLUME: 46, ISSUE: 11
AUTHORS: Gaspar, L. M.; Goncalves, C. I.; Saraiva, C.; Cortez, L.; Amaral, C.; Nobre, E.; Lemos, M. C.;
PUBLISHED: 2023, SOURCE: JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, VOLUME: 46, ISSUE: 11
10
TITLE: Hypoparathyroidism, deafness and renal dysplasia syndrome caused by a GATA3 splice site mutation leading to the activation of a cryptic splice site Full Text
AUTHORS: Goncalves, Catarina I. I.; Carrico, Josianne N. N.; Omar, Omneya M. M.; Abdalla, Ebtesam; Lemos, Manuel C. C.;
PUBLISHED: 2023, SOURCE: FRONTIERS IN ENDOCRINOLOGY, VOLUME: 14
AUTHORS: Goncalves, Catarina I. I.; Carrico, Josianne N. N.; Omar, Omneya M. M.; Abdalla, Ebtesam; Lemos, Manuel C. C.;
PUBLISHED: 2023, SOURCE: FRONTIERS IN ENDOCRINOLOGY, VOLUME: 14
INDEXED IN: WOS
WOS