Markus M. Nöthen

136.4k citations

521 papers · 18.3k · 2 hit papers · h-index 68

Impact in

Biological Psychiatry top 0.2%
Psychiatry and Mental health top 0.2%
- Bipolar Disorder and Treatment
- Schizophrenia research and treatment

Papers in

Genetics 180
- Genetic Associations and Epidemiology 74
- Genetics and Neurodevelopmental Disorders 59
- Genomic variations and chromosomal abnormalities 32
Molecular Biology 155
- Receptor Mechanisms and Signaling 38

Co-authors: Peter Propping (129 shared papers)Sven Cichon (143 shared papers)Marcella Rietschel (175 shared papers)Erik G. Jönsson (18 shared papers)Thomas G. Schulze (60 shared papers)Per Hoffmann (66 shared papers)Göran C. Sedvall (9 shared papers)Michael Knapp (35 shared papers)
Journals: Psychiatric Genetics (34 papers)Molecular Psychiatry (21 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (19 papers)Schizophrenia Research (15 papers)The American Journal of Human Genetics (13 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Markus M. Nöthen

509 papers receiving 17.9k citations

Markus M. Nöthen's Hit Papers

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Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations 2006 · 453 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2006 Journal of Allergy and Clinical Immunology
1999 Molecular Psychiatry

Peers

Countries citing papers authored by Markus M. Nöthen

Since Specialization

Citations

This map shows the geographic impact of Markus M. Nöthen'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 Markus M. Nöthen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus M. Nöthen more than expected).

Fields of papers citing papers by Markus M. Nöthen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Markus M. Nöthen. 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 Markus M. Nöthen. The network helps show where Markus M. Nöthen may publish in the future.

Co-authors

The 25 scholars most cited alongside Markus M. Nöthen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Markus M. Nöthen Line = papers co-authored together Markus M. Nöthen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 521 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Polymorphisms in the dopamine D2 receptor gene and their relationships to striatal dopamine receptor density of healthy volunteers Molecular Psychiatry ·Erik G. Jönsson, Markus M. Nöthen, F Grünhage, Lars Farde, Yoshifumi Nakashima, Peter Propping, Göran C. Sedvall Hit paper breakdown →	1999	593
2	Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder Human Molecular Genetics ·J. Deckert, Marco Catalano, Yana V. Syagailo, Monica Bosi, Olga Okladnova, Daniela Di Bella, Markus M. Nöthen, Pietro Maffei, Petra Franke, J. Fritze, W. Maier, Peter Propping, H. Beckmann, Laura Bellodi, Klaus‐Peter Lesch	1999	483
3	A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder Molecular Psychiatry ·Amber E. Baum, Nirmala Akula, Michael Cabanero, Imer Cardona, Winston Corona, Brygida Klemens, Thomas G. Schulze, Sven Cichon, Marcella Rietschel, Markus M. Nöthen, Alexander Georgi, J Schumacher, Markus Schwarz, Rami Abou Jamra, Susanne Höfels, Peter Propping, Jaya M. Satagopan, Sevilla D. Detera‐Wadleigh, John Hardy, Francis J. McMahon	2007	474
4	Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations Journal of Allergy and Clinical Immunology ·Stephan Weidinger, Thomas Illig, Hansjörg Baurecht, Alan D. Irvine, Elke Rodríguez, Amalia Díaz‐Lacava, Norman Klopp, Stefan Wagenpfeil, Yiwei Zhao, Haihui Liao, Simon P. Lee, (unknown), Claudia Jenneck, Laura Maintz, Tobias Hagemann, Heidrun Behrendt, Johannes Ring, Markus M. Nöthen, W.H. Irwin McLean, Natalija Novak Hit paper breakdown →	2006	453
5	Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells Cell stem cell ·Marc Thier, Philipp Wörsdörfer, Yenal B. Lakes, Raphaela Gorris, Stefan Herms, Thoralf Opitz, Dominic Seiferling, Tamara Quandel, Per Hoffmann, Markus M. Nöthen, Oliver Brüstle, Frank Edenhofer	2012	403
6	G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth Nature Genetics ·Sandra M. Pasternack, Ivar von Kügelgen, Khalid Al Aboud, Young‐Ae Lee, Franz Rüschendorf, Katrin Voß, Axel M. Hillmer, Gerhard J. Molderings, Thomas Franz, Alfredo Ramı́rez, Peter Nürnberg, Markus M. Nöthen, Regina C. Betz	2008	297
7	Increased Activity of Coagulation Factor XII (Hageman Factor) Causes Hereditary Angioedema Type III The American Journal of Human Genetics ·Sven Cichon, Ludovic Martin, Hans Christian Hennies, Felicitas Müller, K. Van Driessche, Anna Karpushova, W. J. Stevens, Roberto Colombo, Thomas Renné, Christian Drouet, Konrad Bork, Markus M. Nöthen	2006	253
8	Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression Biological Psychiatry ·Johannes Schumacher, Rami Abou Jamra, Tim Becker, Stephanie Ohlraun, Norman Klopp, Elisabeth B. Binder, Thomas G. Schulze, Monika Deschner, Christine Schmäl, Susanne Höfels, Astrid Zobel, Thomas Illig, Peter Propping, (unknown), Marcella Rietschel, Markus M. Nöthen, Sven Cichon	2005	247
9	Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder Molecular Psychiatry ·J Schumacher, R Abon Jamra, Jan Freudenberg, Tim Becker, Stephanie Ohlraun, A Otte, Monja Tullius, S. Kovalenko, Ann Van Den Bogaert, W. Maier, Marcella Rietschel, Peter Propping, Markus M. Nöthen, Sven Cichon	2004	232
10	Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene The Lancet ·Julie Williams, Gillian Spurlock, Peter McGuffin, Mike Owen, Jean‐Maurice Mallet, Markus M. Nöthen, Michael Gill, H.N. Aschauer, P-O. Nylander, Fabìo Macciardi	1996	194
11	Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia The American Journal of Human Genetics ·Johannes Schumacher, Heidi Anthoni, Faten Dahdouh, Inke R. König, Axel M. Hillmer, Nadine Kluck, Malou Manthey, Ellen Plume, Andreas Warnke, Helmut Remschmidt, Jutta Hülsmann, Sven Cichon, Cecilia M. Lindgren, Peter Propping, Marco Zucchelli, Andreas Ziegler, Myriam Peyrard‐Janvid, Gerd Schulte‐Körne, Markus M. Nöthen, Juha Kere	2005	180
12	Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature The American Journal of Human Genetics ·Rami Abou Jamra, Orianne Philippe, Annick Raas‐Rothschild, Sebastian Eck, Elisabeth Graf, Rebecca Buchert, Guntram Borck, Arif B. Ekici, Felix F. Brockschmidt, Markus M. Nöthen, Arnold Münnich, Tim M. Strom, André Reis, Laurence Colleaux	2011	170
13	Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia The Lancet ·Julie Williams, Peter McGuffin, Markus M. Nöthen, (unknown)	1997	167
14	Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia Human Genetics ·Jeanette Erdmann, Daphne Shimron‐Abarbanell, Marcella Rietschel, Margot Albus, Wolfgang Maier, Judith Körner, Brigitta Bondy, Kevin Chen, Jean C. Shih, Michael Knapp, Peter Propping, Markus M. Nöthen	1996	159
15	The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease The American Journal of Human Genetics ·Ann Van Den Bogaert, Johannes Schumacher, Thomas G. Schulze, A Otte, Stephanie Ohlraun, S. S. Kovalenko, Tim Becker, Jan Freudenberg, Erik G. Jönsson, Marja Mattila‐Evenden, Göran C. Sedvall, Piotr M. Czerski, Paweł Kapelski, Joanna Hauser, Wolfgang Maier, Marcella Rietschel, Peter Propping, Markus M. Nöthen, Sven Cichon	2003	158
16	Loss-of-Function Mutations in the Keratin 5 Gene Lead to Dowling-Degos Disease The American Journal of Human Genetics ·Regina C. Betz, Laura Planko, Sibylle Eigelshoven, S. Hanneken, Sandra M. Pasternack, Heinrich Büssow, Kris Van Den Bogaert, Joerg Wenzel, Markus Braun‐Falco, Arno Rütten, Michael A. Rogers, Thomas Ruzicka, Markus M. Nöthen, Thomas M. Magin, Roland Kruse	2006	145
17	Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease Nature Genetics ·Regina C. Betz, Benedikt Schoser, Dagmar Kasper, K. Ricker, Alfredo Ramı́rez, Valentin Stein, T. Torbergsen, Youngae Lee, Markus M. Nöthen, Thomas F. Wienker, J.-P. Malin, Peter Propping, André Reis, W. Mortier, Thomas J. Jentsch, Matthias Vorgerd, Christian Kubisch	2001	144
18	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder Molecular Psychiatry ·D T Chen, X Jiang, Nirmala Akula, Yin Yao Shugart, Jens R. Wendland, C J M Steele, Layla Kassem, J-H Park, Nilanjan Chatterjee, Stéphane Jamain, A T A Cheng, Marion Leboyer, Pierandrea Muglia, Thomas G. Schulze, Sven Cichon, Markus M. Nöthen, Marcella Rietschel, (unknown), (unknown)	2011	141
19	Haplotype study of three polymorphisms at the dopamine transporter locus confirm linkage to attention-deficit/hyperactivity disorder Biological Psychiatry ·Cathy L. Barr, Chun Xu, Jamie Kroft, Yu Feng, Karen Wigg, Gwyneth Zai, Rosemary Tannock, Russell Schachar, Molly Malone, Wendy Roberts, Markus M. Nöthen, F Grünhage, David J. Vandenbergh, George R. Uhl, Glen Sunohara, Nicole King, James L. Kennedy	2001	139
20	Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease Molecular Psychiatry ·Jürgen Deckert, Markus M. Nöthen, Petra Franke, Cynthia D. Delmo, J. Fritze, Michael Knapp, Wolfgang Maier, H. Beckmann, Peter Propping	1998	132

About Markus M. Nöthen

Markus M. Nöthen is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Cellular and Molecular Neuroscience and Urology, having authored 521 papers that have together received 18.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (74 papers), Bipolar Disorder and Treatment (61 papers), Genetics and Neurodevelopmental Disorders (59 papers), Neurotransmitter Receptor Influence on Behavior (52 papers), Hair Growth and Disorders (46 papers), Receptor Mechanisms and Signaling (38 papers), Genomic variations and chromosomal abnormalities (32 papers) and Schizophrenia research and treatment (32 papers). The work is most often cited by research in Biological Psychiatry (790 citations), Psychiatry and Mental health (3.3k citations), Cellular and Molecular Neuroscience (3.7k citations), Urology (1.1k citations) and Genetics (4.6k citations). Markus M. Nöthen has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Peter Propping, Sven Cichon, Marcella Rietschel, Erik G. Jönsson, Thomas G. Schulze, Per Hoffmann, Göran C. Sedvall, Michael Knapp, Regina C. Betz and F Grünhage. Their work appears in journals such as Psychiatric Genetics, Molecular Psychiatry, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Schizophrenia Research and The American Journal of Human Genetics.

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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