Hanspeter Goldschmidt

826 total citations
13 papers, 608 citations indexed

About

Hanspeter Goldschmidt is a scholar working on Physiology, Genetics and Endocrine and Autonomic Systems. According to data from OpenAlex, Hanspeter Goldschmidt has authored 13 papers receiving a total of 608 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Physiology, 5 papers in Genetics and 4 papers in Endocrine and Autonomic Systems. Recurrent topics in Hanspeter Goldschmidt's work include Adipose Tissue and Metabolism (4 papers), Regulation of Appetite and Obesity (4 papers) and Genetic Syndromes and Imprinting (2 papers). Hanspeter Goldschmidt is often cited by papers focused on Adipose Tissue and Metabolism (4 papers), Regulation of Appetite and Obesity (4 papers) and Genetic Syndromes and Imprinting (2 papers). Hanspeter Goldschmidt collaborates with scholars based in Germany, United Kingdom and United States. Hanspeter Goldschmidt's co-authors include Anke Hinney, Wolfgang Siegfried, Johannes Hebebrand, Frank Geller, Helmut Remschmidt, H. Schäfer, Anne‐Kathrin Wermter, Sarah Hohmann, Claudia Hess and Andreas Ziegler and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and Journal of Nutrition.

In The Last Decade

Hanspeter Goldschmidt

13 papers receiving 589 citations

Peers

Hanspeter Goldschmidt

EAS

PHYSI

GENET

T. Görg Germany

Megan Greenwald-Yarnell United States

Gregory B. Thomas Australia

Aryana Zavosh United States

Frank H. Koegler United States

R. Schick Germany

Xiaofeng Yan United States

Chi Kin Ip Australia

Kevin Gamber United States

Gábor Mezei Hungary

T. Görg Germany

Hanspeter Goldschmidt

366 ×1.2

EAS

275 ×1.2

149 ×0.8

PHYSI

100 ×0.8

GENET

83 ×0.8

Citations per year, relative to Hanspeter Goldschmidt Hanspeter Goldschmidt (= 1×) peers T. Görg

Countries citing papers authored by Hanspeter Goldschmidt

Since Specialization

Citations

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

Fields of papers citing papers by Hanspeter Goldschmidt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanspeter Goldschmidt

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Hölter, Katja, Anne‐Kathrin Wermter, André Scherag, et al.. (2007). Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3gene in extremely obese children and adolescents. BMC Medical Genetics. 8(1). 21–21. 13 indexed citations

Reichwald, Kathrin, André Scherag, Frank Geller, et al.. (2005). Human Galanin (GAL) and Galanin 1 Receptor (GALR1) Variations Are Not Involved in Fat Intake and Early Onset Obesity. Journal of Nutrition. 135(6). 1387–1392. 21 indexed citations

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

Geller, Frank, Wolfgang Siegfried, Hanspeter Goldschmidt, et al.. (2003). No Evidence for Involvement of the Promoter Polymorphism - 866 G/A of the UCP2 Gene in Childhood-Onset Obesity in Humans. Experimental and Clinical Endocrinology & Diabetes. 111(2). 73–76. 23 indexed citations

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

Hinney, Anke, Sarah Hohmann, Frank Geller, et al.. (2003). Melanocortin-4 Receptor Gene: Case-Control Study and Transmission Disequilibrium Test Confirm that Functionally Relevant Mutations Are Compatible with a Major Gene Effect for Extreme Obesity. The Journal of Clinical Endocrinology & Metabolism. 88(9). 4258–4267. 167 indexed citations

Hinney, Anke, Frank Geller, H. Schäfer, et al.. (2002). No evidence for involvement of the calpain-10 gene `high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity. Molecular Genetics and Metabolism. 76(2). 152–156. 9 indexed citations

Hinney, Anke, Anne Z. Hoch, Frank Geller, et al.. (2002). Ghrelin Gene: Identification of Missense Variants and a Frameshift Mutation in Extremely Obese Children and Adolescents and Healthy Normal Weight Students. The Journal of Clinical Endocrinology & Metabolism. 87(6). 2716–2716. 99 indexed citations

Oeffner, Frank, Thomas Korn, Helmut Roth, et al.. (2001). Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation. International Journal of Obesity. 25(6). 767–769. 6 indexed citations

10.

Hinney, Anke, Frank Geller, G Gerber, et al.. (2001). No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit β3 in body weight regulation. Experimental and Clinical Endocrinology & Diabetes. 109(8). 402–405. 14 indexed citations

11.

Hinney, Anke, Andreas Ziegler, Frank Oeffner, et al.. (2000). Independent Confirmation of a Major Locus for Obesity on Chromosome 10. The Journal of Clinical Endocrinology & Metabolism. 85(8). 2962–2965. 53 indexed citations

12.

Oeffner, Frank, Dorothea Bornholdt, Andreas Ziegler, et al.. (2000). Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents. Acta Diabetologica. 37(2). 93–101. 15 indexed citations

13.

Goldschmidt, Hanspeter & Kligman Am. (1968). Increased sebum secretion following selenium sulfide shampoos.. PubMed. 48(5). 489–91. 12 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.

Explore authors with similar magnitude of impact