João Gonçalves - Concepedia

Author

João Gonçalves

National Institute of Health Dr. Ricardo Jorge ORCID

Also Known As

J Gonçalves, J. Goncalves, J. Gonçalves, JDS Gonçalves, Jennifer Victória Dos Santos Gonçalves, Joao Goncalves, Joao Gonçalves, José Írahe Kasprzykowski Gonçalves, João Goncalves, João Gonçalves

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

National Institute of Health Dr. Ricardo Jorge Universidade do Porto IPO Porto i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto Oregon Health & Science University

About

João Gonçalves is an author at National Institute of Health Dr. Ricardo Jorge specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	507
2	Public Health	4	4	363
3	Biology	1	1	27
4	Cell Biology	1	1	44
5	Molecular Biology	1	1	27

João Gonçalves

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Identification of SOX3 as an XX male sex reversal gene in mice and humans Edwina Sutton, James Hughes, Stefan J. White, Journal of Clinical Investigation SpermatogenesisTestis DifferentiationGeneticsGenomic MechanismMolecular Genetics	2010	276
Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm† Paulo Navarro‐Costa, Paulo Nogueira, M. da G. da C. Carvalho, Human Reproduction	2010	154
Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1 Alexandra M. Lopes, Kenneth I. Aston, Emma E. Thompson, PLoS Genetics	2013	142
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility Margot J. Wyrwoll, Şehime Gülsün Temel, Liina Nagirnaja, The American Journal of Human Genetics	2020	102
A de novo paradigm for male infertility Manon S. Oud, RM Smits, H E Smith, Nature Communications	2022	97
Diverse monogenic subforms of human spermatogenic failure Liina Nagirnaja, Alexandra M. Lopes, Wu‐Lin Charng, Nature Communications	2022	72
CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions Ana Friães, Ana Toste Rêgo, José Maria Aragüés, Molecular Genetics and Metabolism Adrenal GlandMendelian DisorderCongenital Adrenal HyperplasiaGenetic DisorderMedicine	2006	63
No Evidence for an mtDNA Role in Sperm Motility: Data from Complete Sequencing of Asthenozoospermic Males Luı́sa Pereira, João Gonçalves, Ricardo Franco‐Duarte, Molecular Biology and Evolution	2007	60
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia Albert Salas‐Huetos, Frank Tüttelmann, Margot J. Wyrwoll, Human Genetics Genome InstabilityCell DivisionGeneticsMeiosisChromosome Biology	2020	44
Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure Jimmaline J. Hardy, Margot J. Wyrwoll, William M. McFadden, Human Genetics SpermatogenesisGerm Cell BiologyInfertilityDevelopmental BiologyGerm Cell	2021	36

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