Thomas Meitinger

130.1k total citations · 6 hit papers
319 papers, 19.1k citations indexed

About

Thomas Meitinger is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Thomas Meitinger has authored 319 papers receiving a total of 19.1k indexed citations (citations by other indexed papers that have themselves been cited), including 198 papers in Molecular Biology, 116 papers in Genetics and 29 papers in Clinical Biochemistry. Recurrent topics in Thomas Meitinger's work include Mitochondrial Function and Pathology (39 papers), Metabolism and Genetic Disorders (29 papers) and Genetic Associations and Epidemiology (22 papers). Thomas Meitinger is often cited by papers focused on Mitochondrial Function and Pathology (39 papers), Metabolism and Genetic Disorders (29 papers) and Genetic Associations and Epidemiology (22 papers). Thomas Meitinger collaborates with scholars based in Germany, Austria and United States. Thomas Meitinger's co-authors include Tim M. Strom, Holger Prokisch, Peter Lichtner, Michael J. Econs, Bettina Lorenz‐Depiereux, Monika Grabowski, Alfons Meindl, Kenneth E. White, W. Evans and Thomas Illig and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Thomas Meitinger

315 papers receiving 18.7k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

2000 1.2k citations Kenneth E. White, Michael J. Econs et al. profile →
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita

1994 656 citations Tim M. Strom, Thomas Meitinger et al. profile →
Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

2005 616 citations Peter Lichtner, Thomas Meitinger et al. Human Molecular Genetics profile →
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

1994 549 citations Tim M. Strom, Alfons Meindl et al. profile →
A genome-wide perspective of genetic variation in human metabolism

2009 475 citations Christian Gieger, Thomas Meitinger et al. profile →
Mutations in the deubiquitinase gene USP8 cause Cushing's disease

2014 405 citations Martín Reincke, Thomas Meitinger et al. profile →

Peers

Countries citing papers authored by Thomas Meitinger

Since Specialization

Citations

This map shows the geographic impact of Thomas Meitinger's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Thomas Meitinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Meitinger more than expected).

Fields of papers citing papers by Thomas Meitinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas Meitinger. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Thomas Meitinger. The network helps show where Thomas Meitinger may publish in the future.

Co-authorship network of co-authors of Thomas Meitinger

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Meitinger. A scholar is included among the top collaborators of Thomas Meitinger based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Thomas Meitinger. Thomas Meitinger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening Center 2024 ·International Journal of Neonatal Screening ·Gwendolyn Gramer, Saskia B. Wortmann, Junmin Fang‐Hoffmann, Dirk Kohlmüller, Jürgen G. Okun, Holger Prokisch, Thomas Meitinger, Georg F. Hoffmann	2
2	Genome Sequencing for Cases Unsolved by Exome Sequencing: Identifying a Single-Exon Deletion in TBCK in a Case from 30 Years Ago 2024 ·Neuropediatrics ·(unknown), Melanie Brügger, (unknown), Matias Wagner, Elisabeth Graf, Riccardo Berutti, Erik Tilch, (unknown), (unknown), Julia Hoefele, Thomas Meitinger, Juliane Winkelmann, Theresa Brunet	1
3	The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome 2022 ·Clinical Genetics ·Bernt Popp, Melanie Brügger, (unknown), Tobias Bartolomaeus, (unknown), Julia Hentschel, Nataliya Di Donato, Andreas Rump, Janina Gburek‐Augustat, Elisabeth Graf, Matias Wagner, Ina Sorge, Johannes R. Lemke, Thomas Meitinger, Rami Abou Jamra, Vincent Strehlow, Theresa Brunet	2
4	Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders 2022 ·Human Molecular Genetics ·Theresa Brunet, Riccardo Berutti, Veronika Dill, Judith S. Hecker, Daniela Choukair, (unknown), Marcus Deschauer, Janine Diehl‐Schmid, Martin Krenn, Gertrud Eckstein, Elisabeth Graf, Thomas Gasser, Tim M. Strom, Julia Hoefele, Katharina S. Götze, Thomas Meitinger, Matias Wagner	4
5	Association of circulating MR-proADM with all-cause and cardiovascular mortality in the general population: Results from the KORA F4 cohort study 2022 ·PLoS ONE ·Christina Gar, Barbara Thorand, Christian Herder, (unknown), Margit Heier, Christa Meisinger, Annette Peters, Wolfgang Köenig, Wolfgang Rathmann, Michael Roden, Michael Stümvoll, Haïfa Maalmi, Thomas Meitinger, (unknown), Jochen Seißler, Cornelia Then	6
6	Association of renin and aldosterone with glucose metabolism in a Western European population: the KORA F4/FF4 study 2022 ·BMJ Open Diabetes Research & Care ·Cornelia Then, Katrin Ritzel, Christian Herder, (unknown), (unknown), Margit Heier, Christa Meisinger, Annette Peters, Wolfgang Köenig, Wolfgang Rathmann, Michael Roden, Haïfa Maalmi, Michael Stümvoll, Thomas Meitinger, Martin Bidlingmaier, Jochen Seißler, Barbara Thorand, Martín Reincke	6
7	MicroRNA-21–Dependent Macrophage-to-Fibroblast Signaling Determines the Cardiac Response to Pressure Overload 2021 ·Circulation ·Deepak Ramanujam, (unknown), Christina M. Beck, (unknown), (unknown), Anne Dueck, Dena Esfandyari, Gunter Meister, Thomas Meitinger, Christian Schulz, Stefan Engelhardt	108
8	A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy 2020 ·Annals of Clinical and Translational Neurology ·Melanie Brügger, (unknown), Theresa Brunet, Tim M. Strom, Thomas Meitinger, Eberhard Lurz, Ingo Borggraefe, Matias Wagner	4
9	TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge 2020 ·Archives of Gynecology and Obstetrics ·Sabine Grill, Juliane Ramser, Heide Hellebrand, Nicole Pfarr, Melanie Boxberg, Christine Brambs, Nina Ditsch, Alfons Meindl, Eva Groß, Thomas Meitinger, Marion Kiechle, Anne S. Quante	6
10	Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases 2020 ·EBioMedicine ·(unknown), Matias Wagner, Sarah L. Stenton, Tim M. Strom, Saskia B. Wortmann, Holger Prokisch, Thomas Meitinger, Konrad Oexle, Thomas Klopstock	39
11	Biallelic loss‐of‐function variants in RBL2 in siblings with a neurodevelopmental disorder 2020 ·Annals of Clinical and Translational Neurology ·Theresa Brunet, Milena Radivojkov‐Blagojevic, Peter Lichtner, Verena Kraus, Thomas Meitinger, Matias Wagner	8
12	Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing 2019 ·Clinical Genetics ·Dominik S. Westphal, Gloria Leszinski, Esther Rieger‐Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner	22
13	Whole‐exome sequencing revealed a nonsense mutation in STKLD1 causing non‐syndromic pre‐axial polydactyly type A affecting only upper limb 2019 ·Clinical Genetics ·Muhammad Umair, Muhammad Bilal, Raja Hussain Ali, Bader Alhaddad, Farooq Ahmad, Abdullah Abdullah, Tobias B. Haack, Majid Alfadhel, Muhammad Ansar, Thomas Meitinger, Wasim Ahmad	8
14	Genetic Factors Explain a Major Fraction of the 50% Lower Lipoprotein(a) Concentrations in Finns 2018 ·Arteriosclerosis Thrombosis and Vascular Biology ·Gertraud Erhart, Claudia Lamina, Terho Lehtimäki, Pedro Marques‐Vidal, Mika Kähönen, Péter Vollenweider, Olli T. Raitakari, Gérard Waeber, Barbara Thorand, Konstantin Strauch, Christian Gieger, Thomas Meitinger, Annette Peters, Florian Kronenberg, Stefan Coassin	32
15	INSIG2 promoter variant, obesity markers and lipid parameters - No association in a large Slavonic Caucasian population sample. 2010 ·PubMed ·Jaroslav A. Hubáček, (unknown), Romana Bohuslavová, Věra Adámková, Věra Lánská, Thomas Meitinger, Arne Pfeufer	6
16	The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives 2007 ·BMC Medical Genetics ·Cristian Pattaro, Fabio Marroni, (unknown), Deborah Mascalzoni, Irene Pichler, Cláudia B. Volpato, (unknown), Alessandro De Grandi, (unknown), (unknown), Christian Fuchsberger, Martin Gögele, (unknown), (unknown), Стефан Стефанов, Florian D. Vogl, Christian J. Wiedermann, Thomas Meitinger, Peter P. Pramstaller	42
17	Integrative analysis of the mitochondrial proteome 2004 ·mediaTUM (Technical University of Munich) ·Holger Prokisch, Christophe Andréoli, Curt Scharfe, Lars M. Steinmetz, Thomas Meitinger	2
18	Expression profiling in patients with complex IV respiratory chain deficiencies 2002 ·European Journal of Human Genetics ·Konstanze Hörtnagel, Michaela Jaksch, Jobst Landgrebe, (unknown), Thomas Meitinger	3
19	Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 2002 ·European Journal of Human Genetics ·Astrid Golla, Annette Jansson, Juliane Ramser, Heide Hellebrand, R. Zahn, Thomas Meitinger, Bernd H. Belohradsky, Alfons Meindl	130
20	The Autosomal Dominant Hypophosphatemic Rickets (ADHR) Gene Is a Secreted Polypeptide Overexpressed by Tumors that Cause Phosphate Wasting 2001 ·The Journal of Clinical Endocrinology & Metabolism ·Kenneth E. White, Kenneth B. Jonsson, Gwénaëlle Carn, Geeta Hampson, Tim D. Spector, Michael Mannstadt, Bettina Lorenz‐Depiereux, Akimitsu Miyauchi, In Myung Yang, Östen Ljunggren, Thomas Meitinger, Tim M. Strom, Harald Jüppner, Michael J. Econs	231

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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