Volume 140, Issue 1

Search all Human Genetics articles

January 2021

Special Issue on Molecular Genetics of Male Infertility

Issue Editor:

Csilla Krausz

13 articles in this issue

Editorial for the special issue on the molecular genetics of male infertility
Csilla Krausz
Editorial 18 December 2020 Pages: 1 - 5
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Disease gene discovery in male infertility: past, present and future
M. J. Xavier
A. Salas-Huetos
J. A. Veltman
Review Open access 07 July 2020 Pages: 7 - 19
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
The genetic architecture of morphological abnormalities of the sperm tail
Aminata Touré
Guillaume Martinez
Charles Coutton
Review 16 January 2020 Pages: 21 - 42
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player
Tristan Celse
Caroline Cazin
Pierre F. Ray
Original Investigation 27 October 2020 Pages: 43 - 57
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Genetics of the congenital absence of the vas deferens
Eric Bieth
Safouane M. Hamdi
Roger Mieusset
Review Open access 05 February 2020 Pages: 59 - 76
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease
Biagio Cangiano
Du Soon Swee
Marco Bonomi
Review 21 March 2020 Pages: 77 - 111
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice
Henriett Butz
Gábor Nyírő
Attila Patócs
Review Open access 28 March 2020 Pages: 113 - 134
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives
Laura Kasak
Maris Laan
REVIEW 18 January 2020 Pages: 135 - 154
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse
Brendan J. Houston
Donald F. Conrad
Moira K. O’Bryan
Review 04 April 2020 Pages: 155 - 182
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?
Samuele Soraggi
Meritxell Riera
Kristian Almstrup
Review 16 January 2020 Pages: 183 - 201
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
The X chromosome and male infertility
Matthias Vockel
Antoni Riera-Escamilla
Csilla Krausz
Review Open access 24 December 2019 Pages: 203 - 215
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
Albert Salas-Huetos
Frank Tüttelmann
Kenneth I. Aston
Original Investigation 19 November 2020 Pages: 217 - 227
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility
Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia
Albert Salas-Huetos
Frank Tüttelmann
Kenneth I. Aston
Correction 30 December 2020 Pages: 229 - 229
Part of 2 collections:

Molecular genetics of male infertility

Molecular genetics of male infertility

Volume 140, Issue 1

Editorial for the special issue on the molecular genetics of male infertility

Disease gene discovery in male infertility: past, present and future

The genetic architecture of morphological abnormalities of the sperm tail

Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player

Genetics of the congenital absence of the vas deferens

Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease

Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice

Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives

A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse

Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?

The X chromosome and male infertility

Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia

Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia

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