Publications by authors named "Thomas Meitinger"

Claim this Profile
T
The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.
Kajus Merkevicius, Dmitrii Smirnov, Lea D Schlieben, Rebecca Ganetzky, René G Feichtinger, Thomas Meitinger

Brain· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De Novo Variants in PPFIA2 in Individuals With Neurodevelopmental Disorders.
Theresa Brunet, Michael Zech, Ulrich A Schatz, Miriam Adamovičová, Matias Wagner, Thomas Meitinger

Am J Med Genet A· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Combined genomics and proteomics unveils elusive variants and vast aetiologic heterogeneity in dystonia.
Michael Zech, Ivana Dzinovic, Matej Skorvanek, Philip Harrer, Jan Necpal, Thomas Meitinger

Brain· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Thomas Meitinger

Nat Genet· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical scores fail to sufficiently identify children with Familial Hypercholesterolemia.
Raphael S Schmieder, Johannes Krefting, Sara Ates, Lea D Schlieben, Stefan Arens, Thomas Meitinger

Eur J Prev Cardiol· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pleiotropic effects of MORC2 derive from its epigenetic signature.
Fatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, Robert Kopajtich, Masahiro Ando, Thomas Meitinger

Brain· April 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome Sequencing for Cases Unsolved by Exome Sequencing: Identifying a Single-Exon Deletion in TBCK in a Case from 30 Years Ago.
Maureen Jacob, Melanie Brugger, Stephanie Andres, Matias Wagner, Elisabeth Graf, Thomas Meitinger

Neuropediatrics· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Thomas Meitinger

Nat Genet· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Axel Schmidt, Magdalena Danyel, Kathrin Grundmann, Theresa Brunet, Hannah Klinkhammer, Thomas Meitinger

Nat Genet· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson Mendes de Oliveira, Thomas Meitinger

Nat Genet· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bidirectional modulation of TCA cycle metabolites and anaplerosis by metformin and its combination with SGLT2i.
Makoto Harada, Jonathan Adam, Marcela Covic, Jianhong Ge, Stefan Brandmaier, Thomas Meitinger

Cardiovasc Diabetol· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic landscape of pediatric acute liver failure of indeterminate origin.
Dominic Lenz, Lea D Schlieben, Masaru Shimura, Alyssa Bianzano, Dmitrii Smirnov, Thomas Meitinger

Hepatology· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, Julia Calzada-Wack, Yong Li, Thomas Meitinger

Kidney Int· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Ken Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, Henry J Taylor, Xianyong Yin, Thomas Meitinger

Nature· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke.
Theresa Brunet, Benedikt Zott, Victoria Lieftüchter, Dominic Lenz, Axel Schmidt, Thomas Meitinger

Genet Med· February 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening Center.
Gwendolyn Gramer, Saskia B Wortmann, Junmin Fang-Hoffmann, Dirk Kohlmüller, Jürgen G Okun, Thomas Meitinger

Int J Neonatal Screen· February 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications.
Rosalie B T M Sterenborg, Inga Steinbrenner, Yong Li, Melissa N Bujnis, Tatsuhiko Naito, Thomas Meitinger

Nat Commun· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Lisa de las Fuentes, Karen L Schwander, Michael R Brown, Amy R Bentley, Thomas W Winkler, Thomas Meitinger

Front Genet· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Circulating metabolites modulated by diet are associated with depression.
Ashley van der Spek, Isobel D Stewart, Brigitte Kühnel, Maik Pietzner, Tahani Alshehri, Thomas Meitinger

Mol Psychiatry· September 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic insights into resting heart rate and its role in cardiovascular disease.
Yordi J van de Vegte, Ruben N Eppinga, M Yldau van der Ende, Yanick P Hagemeijer, Yuvaraj Mahendran, Thomas Meitinger

Nat Commun· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience.
Korbinian M Riedhammer, Jasmina Ćomić, Velibor Tasic, Jovana Putnik, Nora Abazi-Emini, Thomas Meitinger

Eur J Hum Genet· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Katherine A Kentistou, Lena R Kaisinger, Stasa Stankovic, Marc Vaudel, Edson M de Oliveira, Thomas Meitinger

medRxiv· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus.
Iain Mathieson, Felix R Day, Nicola Barban, Felix C Tropf, David M Brazel, Thomas Meitinger

Nat Hum Behav· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Implication of dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, Julia Calzada-Wack, Yong Li, Thomas Meitinger

medRxiv· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.
Ken Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, Henry J Taylor, Xianyong Yin, Thomas Meitinger

medRxiv· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis