Publications by authors named "Birgit Stallmeyer"

Claim this Profile

Mentions over time

Mentions by platform

Video Views

29

Total Likes

0

Extended Reach

4,353

Social Features

5
D
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia.
Ann-Kristin Dicke, Adrian Pilatz, Margot J Wyrwoll, Margus Punab, Christian Ruckert, Liina Nagirnaja, Kenneth I Aston, Donald F Conrad, Sara Di Persio, Nina Neuhaus

Commun Biol· March 2023

Videos about Article: user

1 4

View All Article and Social Media Activity
F
Functional and clinical insights into nuclear receptor variants for advancing precision diagnostics in male infertility.
Avinash S Gaikwad, Margot J Wyrwoll, Sophie A Koser, Jana Emich, Johanna Kuß, Birgit Stallmeyer

EBioMedicine· September 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
How exome sequencing improves the diagnostics and management of men with non-syndromic infertility.
Birgit Stallmeyer, Ann-Kristin Dicke, Frank Tüttelmann

Andrology· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NXT2 is a key component of the RNA nuclear export factor complex in the human testis and essential for spermatogenesis.
Ann-Kristin Dicke, Ammar Ahmedani, Lin Ma, Leonie Herrmann, Godfried W van der Heijden, Birgit Stallmeyer

Nat Commun· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes.
Nadja Rotte, Jessica E M Dunleavy, Michelle D Runkel, Lina Bosse, Daniela Fietz, Birgit Stallmeyer

EMBO Mol Med· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility.
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh

Nat Commun· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Scrutinizing the human TEX genes in the context of human male infertility.
Marie H Sieper, Avinash S Gaikwad, Marion Fros, Philipp Weber, Sara Di Persio, Birgit Stallmeyer

Andrology· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
C19ORF84 connects piRNA and DNA methylation machineries to defend the mammalian germ line.
Ansgar Zoch, Gabriela Konieczny, Tania Auchynnikava, Birgit Stallmeyer, Nadja Rotte

Mol Cell· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation.
Samuel Young, Christian Schiffer, Alice Wagner, Jannika Patz, Anton Potapenko, Birgit Stallmeyer

J Clin Invest· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertility.
Ann-Kristin Dicke, Jakob Albrethsen, Bradley L Hoare, Margot J Wyrwoll, Alexander S Busch, Birgit Stallmeyer

Hum Reprod· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.
Margot J Wyrwoll, Nils Köckerling, Matthias Vockel, Ann-Kristin Dicke, Nadja Rotte, Birgit Stallmeyer

Eur Urol· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.
Kim Joana Westerich, Solveig Reinecke, Jana Emich, Margot Julia Wyrwoll, Birgit Stallmeyer

Hum Reprod· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The second PI(3,5)P binding site in the helix of KCNQ1 stabilizes PIP-at the primary site with potential consequences on intermediate-to-open state transition.
Maurice Dellin, Ina Rohrbeck, Purva Asrani, Julian A Schreiber, Nadine Ritter, Birgit Stallmeyer

Biol Chem· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional assessment of DMRT1 variants and their pathogenicity for isolated male infertility.
Jana Emich, Avinash S Gaikwad, Birgit Stallmeyer, Daniela Fietz, Hans-Christian Schuppe

Fertil Steril· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy.
Susanne Rinné, Birgit Stallmeyer, Alexandra Pinggera, Michael F Netter, Lina A Matschke

Int J Mol Sci· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.
Margot J Wyrwoll, Channah M Gaasbeek, Ieva Golubickaite, Rytis Stakaitis, Manon S Oud, Birgit Stallmeyer

Am J Hum Genet· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Non-syndromal mitral valve prolapse (MVP): a common entity, but not commonly associated with or mutations.
Katharina Uphoff, Sven Dittmann, Patricia Ott, Birgit Stallmeyer, Eric Schulze-Bahr

J Thorac Dis· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Birgit Stallmeyer

Nat Genet· May 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Birgit Stallmeyer

Nat Genet· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death.
Björn Fischer, Sven Dittmann, Andreas Brodehl, Andreas Unger, Birgit Stallmeyer

Int J Cardiol· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls.
Roddy Walsh, Najim Lahrouchi, Rafik Tadros, Florence Kyndt, Charlotte Glinge, Birgit Stallmeyer

Genet Med· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel Loss-Of-Function Mutation.
Dominique Endres, Niels Decher, Isabell Röhr, Kirsty Vowinkel, Katharina Domschke, Birgit Stallmeyer

Int J Mol Sci· November 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
POPDC2 a novel susceptibility gene for conduction disorders.
Susanne Rinné, Beatriz Ortiz-Bonnin, Birgit Stallmeyer, Aytug K Kiper, Lisa Fortmüller

J Mol Cell Cardiol· August 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Najim Lahrouchi, Rafik Tadros, Lia Crotti, Yuka Mizusawa, Pieter G Postema, Birgit Stallmeyer

Circulation· July 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition.
Jason D Roberts, S Yukiko Asaki, Andrea Mazzanti, J Martijn Bos, Izabela Tuleta, Birgit Stallmeyer

Circulation· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis