Susann Friedel

2.5k total citations
27 papers, 1.6k citations indexed

About

Susann Friedel is a scholar working on Genetics, Psychiatry and Mental health and Cognitive Neuroscience. According to data from OpenAlex, Susann Friedel has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Psychiatry and Mental health and 6 papers in Cognitive Neuroscience. Recurrent topics in Susann Friedel's work include Attention Deficit Hyperactivity Disorder (8 papers), Genetic Associations and Epidemiology (6 papers) and Autism Spectrum Disorder Research (5 papers). Susann Friedel is often cited by papers focused on Attention Deficit Hyperactivity Disorder (8 papers), Genetic Associations and Epidemiology (6 papers) and Autism Spectrum Disorder Research (5 papers). Susann Friedel collaborates with scholars based in Germany, United Kingdom and United States. Susann Friedel's co-authors include Johannes Hebebrand, Anke Hinney, H. Schäfer, Astrid Dempfle, Helmut Remschmidt, Günter Brönner, André Scherag, Timo D. Müller, Thuy Trang Nguyen and Harald Grallert and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and PEDIATRICS.

In The Last Decade

Susann Friedel

27 papers receiving 1.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Susann Friedel Germany 22 491 407 343 325 293 27 1.6k
Joanne Voisey Australia 24 297 0.6× 175 0.4× 128 0.4× 126 0.4× 206 0.7× 81 1.7k
Ivaldo Silva Brazil 16 212 0.4× 130 0.3× 146 0.4× 527 1.6× 146 0.5× 41 1.3k
Song‐Ping Han China 20 159 0.3× 191 0.5× 449 1.3× 118 0.4× 287 1.0× 46 2.0k
Pradeep Sahota United States 21 143 0.3× 353 0.9× 813 2.4× 351 1.1× 206 0.7× 70 1.6k
Susann Scherag Germany 17 184 0.4× 189 0.5× 149 0.4× 209 0.6× 50 0.2× 19 821
Rachel Maayan Israel 30 157 0.3× 563 1.4× 152 0.4× 110 0.3× 500 1.7× 78 2.5k
Maria A. Morgan United States 14 230 0.5× 234 0.6× 362 1.1× 84 0.3× 431 1.5× 30 1.5k
Chrisana Gundlah United States 14 473 1.0× 134 0.3× 109 0.3× 156 0.5× 551 1.9× 14 1.7k
J.F. Cubells United States 15 195 0.4× 363 0.9× 195 0.6× 76 0.2× 899 3.1× 21 2.0k
Masaaki Narita Japan 17 352 0.7× 182 0.4× 563 1.6× 146 0.4× 384 1.3× 34 1.2k

Countries citing papers authored by Susann Friedel

Since Specialization
Citations

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

Fields of papers citing papers by Susann Friedel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susann Friedel. 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 Susann Friedel. The network helps show where Susann Friedel may publish in the future.

Co-authorship network of co-authors of Susann Friedel

This figure shows the co-authorship network connecting the top 25 collaborators of Susann Friedel. A scholar is included among the top collaborators of Susann Friedel 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 Susann Friedel. Susann Friedel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Konrad, Kerstin, Astrid Dempfle, Susann Friedel, et al.. (2009). Familiality and molecular genetics of attention networks in ADHD. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 148–158. 21 indexed citations
2.
Hammer, Christian, Johannes Kapeller, Max Endele, et al.. (2009). Functional variants of the serotonin receptor type 3A and B gene are associated with eating disorders. Pharmacogenetics and Genomics. 19(10). 790–799. 30 indexed citations
3.
Vogel, Carla Ivane Ganz, Brandon Greene, André Scherag, et al.. (2009). Non-replication of an association of CTNNBL1polymorphisms and obesity in a population of Central European ancestry. BMC Medical Genetics. 10(1). 14–14. 18 indexed citations
4.
Albayrak, Özgür, Susann Friedel, Benno G. Schimmelmann, Anke Hinney, & Johannes Hebebrand. (2008). Genetic aspects in attention-deficit/hyperactivity disorder. Journal of Neural Transmission. 115(2). 305–315. 44 indexed citations
5.
Reinehr, Thomas, Johannes Hebebrand, Susann Friedel, et al.. (2008). Lifestyle Intervention in Obese Children With Variations in the Melanocortin 4 Receptor Gene. Obesity. 17(2). 382–389. 114 indexed citations
6.
7.
Friedel, Susann, Kathrin Reichwald, André Scherag, et al.. (2007). Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13. BMC Genetics. 8(1). 17–17. 26 indexed citations
8.
Schimmelmann, Benno G., Susann Friedel, Astrid Dempfle, et al.. (2007). No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD. Journal of Neural Transmission. 114(4). 523–526. 25 indexed citations
9.
Hinney, Anke, Thuy Trang Nguyen, André Scherag, et al.. (2007). Genome Wide Association (GWA) Study for Early Onset Extreme Obesity Supports the Role of Fat Mass and Obesity Associated Gene (FTO) Variants. PLoS ONE. 2(12). e1361–e1361. 384 indexed citations
10.
Okamura, Naoe, Kenji Hashimoto, Masaomi Iyo, et al.. (2007). Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 31(7). 1444–1448. 107 indexed citations
11.
Heiser, Philip, Astrid Dempfle, Susann Friedel, et al.. (2006). Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample. Journal of Neural Transmission. 114(4). 513–521. 32 indexed citations
12.
Dempfle, Astrid, Stefan A. Wudy, Kathrin Saar, et al.. (2006). Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies. Human Molecular Genetics. 15(18). 2772–2783. 37 indexed citations
13.
Walitza, Susanne, Tobias Renner, Astrid Dempfle, et al.. (2005). Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder. Molecular Psychiatry. 10(12). 1126–1132. 134 indexed citations
14.
Hebebrand, Johannes, Astrid Dempfle, Kathrin Saar, et al.. (2005). A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs. Molecular Psychiatry. 11(2). 196–205. 89 indexed citations
15.
Friedel, Susann, Frank Geller, Astrid Dempfle, et al.. (2004). Mutation screen of the brain derived neurotrophic factor gene (BDNF): Identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention‐deficit/hyperactivity disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 132B(1). 96–99. 123 indexed citations
16.
Hinney, Anke, Susann Friedel, Helmut Remschmidt, & Johannes Hebebrand. (2004). Genetic Risk Factors in Eating Disorders. PubMed. 4(4). 209–223. 29 indexed citations
17.
Heiser, Philip, Susann Friedel, Astrid Dempfle, et al.. (2004). Molecular genetic aspects of attention-deficit/hyperactivity disorder. Neuroscience & Biobehavioral Reviews. 28(6). 625–641. 52 indexed citations
18.
Wang, Haijun, Frank Geller, Astrid Dempfle, et al.. (2004). Ghrelin Receptor Gene: Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Short Normal Stature. The Journal of Clinical Endocrinology & Metabolism. 89(1). 157–162. 112 indexed citations
19.
Saar, Kathrin, Frank Geller, Franz Rüschendorf, et al.. (2003). Genome Scan for Childhood and Adolescent Obesity in German Families. PEDIATRICS. 111(2). 321–327. 53 indexed citations
20.
Hebebrand, Johannes, et al.. (2003). Perspectives: molecular genetic research in human obesity. Obesity Reviews. 4(3). 139–146. 47 indexed citations

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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