Hans Knoblauch

2.3k total citations
40 papers, 1.3k citations indexed

About

Hans Knoblauch is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Hans Knoblauch has authored 40 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 15 papers in Molecular Biology and 11 papers in Surgery. Recurrent topics in Hans Knoblauch's work include Lipoproteins and Cardiovascular Health (7 papers), Genetic Syndromes and Imprinting (6 papers) and Cholesterol and Lipid Metabolism (6 papers). Hans Knoblauch is often cited by papers focused on Lipoproteins and Cardiovascular Health (7 papers), Genetic Syndromes and Imprinting (6 papers) and Cholesterol and Lipid Metabolism (6 papers). Hans Knoblauch collaborates with scholars based in Germany, Switzerland and United States. Hans Knoblauch's co-authors include Herbert Schuster, Friedrich C. Luft, Andreas Busjahn, Hans‐Dieter Faulhaber, Bernhard Horsthemke, Karin Buiting, Bertram Müller‐Myhsok, Jürgen Bohlender, Margit Knoblauch and Lutz Roewer and has published in prestigious journals such as Circulation, Nature Genetics and Stroke.

In The Last Decade

Hans Knoblauch

38 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hans Knoblauch Germany 22 670 608 308 260 207 40 1.3k
Nancy L. Heard‐Costa United States 18 493 0.7× 371 0.6× 173 0.6× 106 0.4× 92 0.4× 37 1.2k
Min Jin Go South Korea 18 340 0.5× 315 0.5× 85 0.3× 221 0.8× 151 0.7× 34 1.1k
Sylvia Bähring Germany 19 278 0.4× 823 1.4× 225 0.7× 269 1.0× 147 0.7× 37 1.3k
Randall W. Whitcomb United States 22 451 0.7× 950 1.6× 198 0.6× 1.1k 4.1× 130 0.6× 38 2.7k
Naoko Iwasaki Japan 20 598 0.9× 646 1.1× 48 0.2× 313 1.2× 525 2.5× 61 1.4k
J. Neulen Germany 23 314 0.5× 355 0.6× 80 0.3× 223 0.9× 63 0.3× 75 1.8k
Yunhua L. Muller United States 22 462 0.7× 660 1.1× 63 0.2× 193 0.7× 251 1.2× 54 1.2k
L E Underwood United States 17 283 0.4× 518 0.9× 164 0.5× 1.1k 4.1× 188 0.9× 19 1.6k
S. Longobardi Italy 19 157 0.2× 419 0.7× 238 0.8× 944 3.6× 147 0.7× 31 1.4k
Martine Imbert–Teboul France 28 158 0.2× 1.4k 2.2× 173 0.6× 249 1.0× 143 0.7× 54 2.1k

Countries citing papers authored by Hans Knoblauch

Since Specialization
Citations

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

Fields of papers citing papers by Hans Knoblauch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hans Knoblauch

This figure shows the co-authorship network connecting the top 25 collaborators of Hans Knoblauch. A scholar is included among the top collaborators of Hans Knoblauch 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 Hans Knoblauch. Hans Knoblauch 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.
Moser, Sylvain, Hans Knoblauch, Bertram Müller‐Myhsok, et al.. (2025). CATT haplotype of the FKBP5 gene and dissociative phenomenology. Scientific Reports. 15(1). 28581–28581.
2.
Vermeulen, Mark, Andreas Wollstein, Kristiaan J. van der Gaag, et al.. (2009). Improving global and regional resolution of male lineage differentiation by simple single-copy Y-chromosomal short tandem repeat polymorphisms. Forensic Science International Genetics. 3(4). 205–213. 75 indexed citations
3.
Kayser, Manfred, Mark Vermeulen, Hans Knoblauch, et al.. (2007). Relating two deep-rooted pedigrees from Central Germany by high-resolution Y-STR haplotyping. Forensic Science International Genetics. 1(2). 125–128. 31 indexed citations
4.
5.
Jefferies, Craig, Paul L. Hofman, Hans Knoblauch, et al.. (2004). Insulin resistance in healthy prepubertal twins. The Journal of Pediatrics. 144(5). 608–613. 30 indexed citations
6.
Knoblauch, Hans, C. Tennstedt, Wolfgang Brueck, et al.. (2003). Two brothers with findings resembling congenital intrauterine infection‐like syndrome (pseudo‐TORCH syndrome). American Journal of Medical Genetics Part A. 120A(2). 261–265. 21 indexed citations
7.
Vergopoulos, Athanasios, Hans Knoblauch, & Herbert Schuster. (2002). DNA Testing for Familial Hypercholesterolemia. PubMed. 2(4). 253–262. 10 indexed citations
8.
Bauerfeind, Anja, Hans Knoblauch, Herbert Schuster, Friedrich C. Luft, & J. Reich. (2002). Single Nucleotide Polymorphism Haplotypes in the Cholesteryl-Ester Transfer Protein (CETP) Gene and Lipid Phenotypes. Human Heredity. 54(4). 166–173. 12 indexed citations
9.
Knoblauch, Hans. (2002). Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population. Human Molecular Genetics. 11(12). 1477–1485. 52 indexed citations
10.
Cai, Li, Amanda L. Lumsden, Ulf P. Guenther, et al.. (2001). A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum. Journal of Molecular Medicine. 79(9). 536–546. 45 indexed citations
11.
Knoblauch, Hans, Herbert Schuster, Friedrich C. Luft, & J. Reich. (2000). A pathway model of lipid metabolism to predict the effect of genetic variability on lipid levels. Journal of Molecular Medicine. 78(9). 507–515. 25 indexed citations
12.
Busjahn, Andreas, Hans Knoblauch, Hans‐Dieter Faulhaber, et al.. (2000). A region on chromosome 3 is linked to dizygotic twinning. Nature Genetics. 26(4). 398–399. 25 indexed citations
13.
Schiller, Simone, Stephanie Spranger, Birgit Schechinger, et al.. (2000). Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome. European Journal of Human Genetics. 8(1). 54–62. 115 indexed citations
14.
Pei, Wei-dong, Heike Baron, Bertram Müller‐Myhsok, et al.. (2000). Support for linkage of familial combined hyperlipidemia to chromosome 1q21–q23 in Chinese and German families. Clinical Genetics. 57(1). 29–34. 64 indexed citations
15.
Boeckel, Thomas P. Van, Athanasios Vergopoulos, Sylvia Bähring, et al.. (1999). A new mutation in the elastin gene causing supravalvular aortic stenosis. The American Journal of Cardiology. 83(7). 1141–1143. 15 indexed citations
16.
Knoblauch, Hans, Michael Urban, & Sigrid Tinschert. (1999). Autosomal recessive versus autosomal dominant inheritance in Larsen syndrome: report of two affected sisters.. PubMed. 10(3). 315–20. 5 indexed citations
17.
Pfeufer, Arne, Andreas Busjahn, Athanasios Vergopoulos, et al.. (1998). Chymase gene locus is not associated with myocardial infarction and is not linked to heart size or blood pressure. The American Journal of Cardiology. 82(8). 979–981. 7 indexed citations
18.
Dittrich, Bärbel, Hans Knoblauch, Karin Buiting, & Bernhard Horsthemke. (1993). Characterization of a DNA Sequence Family in the Prader-Willi/Angelman Syndrome Chromosome Region in 15q11-q13. Genomics. 16(1). 269–271. 4 indexed citations
19.
Robinson, Wendy P., Isabel Lorda‐Sánchez, S Malcolm, et al.. (1993). Increased Parental Ages and Uniparental Disomy 15: A Paternal Age Effect?. European Journal of Human Genetics. 1(4). 280–286. 42 indexed citations
20.
Knoblauch, Hans, et al.. (1992). Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Human Genetics. 90(3). 313–5. 171 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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