Christine Herold

4.6k total citations
26 papers, 718 citations indexed

About

Christine Herold is a scholar working on Genetics, Molecular Biology and Urology. According to data from OpenAlex, Christine Herold has authored 26 papers receiving a total of 718 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Urology. Recurrent topics in Christine Herold's work include Genetic Associations and Epidemiology (16 papers), Hair Growth and Disorders (6 papers) and Genetic Mapping and Diversity in Plants and Animals (6 papers). Christine Herold is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Hair Growth and Disorders (6 papers) and Genetic Mapping and Diversity in Plants and Animals (6 papers). Christine Herold collaborates with scholars based in Germany, United States and Netherlands. Christine Herold's co-authors include Tim Becker, Felix F. Brockschmidt, Max P. Baur, Michael Steffens, Markus M. Nöthen, Manuel Mattheisen, Roland Kruse, S. Hanneken, Sibylle Eigelshoven and Rudolph E. Tanzi and has published in prestigious journals such as Bioinformatics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Christine Herold

26 papers receiving 700 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christine Herold Germany 15 319 253 164 106 84 26 718
Bryce J. Cowan Canada 12 637 2.0× 65 0.3× 37 0.2× 89 0.8× 92 1.1× 18 983
J.W. Delleman Netherlands 17 360 1.1× 275 1.1× 15 0.1× 60 0.6× 137 1.6× 45 872
S Hayasaka Japan 17 279 0.9× 61 0.2× 23 0.1× 136 1.3× 33 0.4× 79 1.0k
Denny Schanze Germany 18 393 1.2× 223 0.9× 7 0.0× 37 0.3× 50 0.6× 55 749
Joe J. Hoo United States 20 388 1.2× 510 2.0× 25 0.2× 20 0.2× 67 0.8× 54 900
Ada Rosenmann Israel 16 347 1.1× 252 1.0× 17 0.1× 33 0.3× 146 1.7× 36 650
V Der Kaloustian United States 9 296 0.9× 149 0.6× 18 0.1× 19 0.2× 44 0.5× 14 553
Jeppe Dyrberg Andersen Denmark 13 255 0.8× 142 0.6× 20 0.1× 101 1.0× 148 1.8× 57 509
A. Franceschetti Switzerland 12 288 0.9× 128 0.5× 13 0.1× 45 0.4× 108 1.3× 75 633
Nallathambi Jeyabalan India 18 355 1.1× 172 0.7× 7 0.0× 19 0.2× 82 1.0× 31 841

Countries citing papers authored by Christine Herold

Since Specialization
Citations

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

Fields of papers citing papers by Christine Herold

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Herold

This figure shows the co-authorship network connecting the top 25 collaborators of Christine Herold. A scholar is included among the top collaborators of Christine Herold 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 Christine Herold. Christine Herold 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.
Herold, Christine, Kristina Mullin, Tian Liu, et al.. (2016). Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer’s disease with OSBPL6, PTPRG, and PDCL3. Molecular Psychiatry. 21(11). 1608–1612. 72 indexed citations
2.
Liu, Fan, Merel A. Hamer, Stefanie Heilmann‐Heimbach, et al.. (2015). Prediction of male-pattern baldness from genotypes. European Journal of Human Genetics. 24(6). 895–902. 41 indexed citations
3.
Park, Suyeon, Sungyoung Lee, Young Lee, et al.. (2015). Adjusting heterogeneous ascertainment bias for genetic association analysis with extended families. BMC Medical Genetics. 16(1). 62–62. 7 indexed citations
4.
Lacour, André, Dmitriy Drichel, Christine Herold, et al.. (2015). Novel genetic matching methods for handling population stratification in genome-wide association studies. BMC Bioinformatics. 16(1). 84–84. 6 indexed citations
5.
Drichel, Dmitriy, Christine Herold, André Lacour, et al.. (2014). Rare Variant Testing of Imputed Data: An Analysis Pipeline Typified. Human Heredity. 78(3-4). 164–178. 1 indexed citations
6.
Drichel, Dmitriy, et al.. (2014). Analysis of the progression of systolic blood pressure using imputation of missing phenotype values. BMC Proceedings. 8(S1). S83–S83. 4 indexed citations
7.
Heilmann‐Heimbach, Stefanie, Dale R. Nyholt, F.F. Brockschmidt, et al.. (2013). No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia. Queensland's institutional digital repository (The University of Queensland). 2 indexed citations
8.
Herold, Christine, Alfredo Ramı́rez, Dmitriy Drichel, et al.. (2013). A One-Degree-of-Freedom Test for Supra-Multiplicativity of SNP Effects. PLoS ONE. 8(10). e78038–e78038. 1 indexed citations
9.
Redler, Silke, F.F. Brockschmidt, Christine Herold, et al.. (2012). Investigation of selected cytokine genes suggests that IL2RA and the TNF / LTA locus are risk factors for severe alopecia areata. British Journal of Dermatology. 167(6). 1360–1365. 32 indexed citations
10.
Meesters, Christian, Markus Leber, Christine Herold, et al.. (2012). Quick, “Imputation-free” meta-analysis with proxy-SNPs. BMC Bioinformatics. 13(1). 231–231. 5 indexed citations
11.
Herold, Christine, et al.. (2012). Integrated Genome-Wide Pathway Association Analysis with INTERSNP. Human Heredity. 73(2). 63–72. 8 indexed citations
12.
Redler, Silke, Felix F. Brockschmidt, Christine Herold, et al.. (2012). Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance. Journal of Investigative Dermatology. 132(9). 2192–2197. 98 indexed citations
13.
Becker, Tim, Christine Herold, Christian Meesters, Manuel Mattheisen, & Max P. Baur. (2010). Significance Levels in Genome-Wide Interaction Analysis (GWIA). Annals of Human Genetics. 75(1). 29–35. 19 indexed citations
14.
Steffens, Michael, Tim Becker, Thomas Sander, et al.. (2010). Feasible and Successful: Genome-Wide Interaction Analysis Involving All 1.9 × 10<sup>11</sup> Pair-Wise Interaction Tests. Human Heredity. 69(4). 268–284. 19 indexed citations
15.
Becker, Tim, Antònia Flaquer, Felix F. Brockschmidt, Christine Herold, & Michael Steffens. (2009). Evaluation of Potential Power Gain with Imputed Genotypes in Genome-Wide Association Studies. Human Heredity. 68(1). 23–34. 3 indexed citations
16.
Schumacher, Johannes, Gonzalo Laje, Rami Abou Jamra, et al.. (2009). The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. Human Molecular Genetics. 18(14). 2719–2727. 67 indexed citations
17.
Scholl, Hendrik P. N., Monika Fleckenstein, Lars G. Fritsche, et al.. (2009). CFH, C3 and ARMS2 Are Significant Risk Loci for Susceptibility but Not for Disease Progression of Geographic Atrophy Due to AMD. PLoS ONE. 4(10). e7418–e7418. 74 indexed citations
18.
Herold, Christine, Michael Steffens, Felix F. Brockschmidt, Max P. Baur, & Tim Becker. (2009). INTERSNP: genome-wide interaction analysis guided by a priori information. Bioinformatics. 25(24). 3275–3281. 102 indexed citations
19.
Redler, Silke, F.F. Brockschmidt, Kathrin Giehl, et al.. (2009). The TRAF1/C5 locus confers risk for familial and severe alopecia areata. British Journal of Dermatology. 162(4). 866–869. 16 indexed citations
20.
Herold, Christine & Tim Becker. (2008). Genetic association analysis with FAMHAP: a major program update. Bioinformatics. 25(1). 134–136. 54 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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