Jochen Hecht

10.3k total citations
77 papers, 3.5k citations indexed

About

Jochen Hecht is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Jochen Hecht has authored 77 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 22 papers in Genetics and 8 papers in Epidemiology. Recurrent topics in Jochen Hecht's work include Genomics and Chromatin Dynamics (11 papers), Genomics and Phylogenetic Studies (8 papers) and Congenital limb and hand anomalies (7 papers). Jochen Hecht is often cited by papers focused on Genomics and Chromatin Dynamics (11 papers), Genomics and Phylogenetic Studies (8 papers) and Congenital limb and hand anomalies (7 papers). Jochen Hecht collaborates with scholars based in Germany, Spain and United States. Jochen Hecht's co-authors include Stefan Mundlos, Peter Krawitz, Peter N. Robinson, Verena Heinrich, Christian Haass, Alexander Hruscha, Bettina Schmid, Richard Reinhardt, Sigmar Stricker and Ulrike Krüger and has published in prestigious journals such as Nucleic Acids Research, Circulation and Journal of Clinical Investigation.

In The Last Decade

Jochen Hecht

75 papers receiving 3.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jochen Hecht Germany 32 2.1k 987 433 284 280 77 3.5k
Stefan Krebs Germany 33 2.6k 1.2× 578 0.6× 693 1.6× 239 0.8× 314 1.1× 134 4.5k
Licia Selleri United States 42 3.3k 1.6× 1.1k 1.1× 622 1.4× 165 0.6× 156 0.6× 110 5.0k
Kyle Vogan United States 18 2.2k 1.0× 791 0.8× 351 0.8× 126 0.4× 344 1.2× 45 3.4k
Brigitte Royer‐Pokora Germany 37 3.8k 1.8× 1.3k 1.3× 682 1.6× 189 0.7× 246 0.9× 118 5.5k
T Sekiya Japan 20 2.0k 0.9× 826 0.8× 313 0.7× 298 1.0× 372 1.3× 53 4.3k
Didier Décimo France 29 3.3k 1.5× 998 1.0× 441 1.0× 99 0.3× 263 0.9× 56 4.3k
Louise van der Weyden United Kingdom 35 2.7k 1.2× 700 0.7× 941 2.2× 200 0.7× 545 1.9× 97 4.7k
David Roazen United States 2 2.1k 1.0× 1.8k 1.8× 240 0.6× 609 2.1× 271 1.0× 2 4.3k
Khalid Shakir United States 2 2.1k 1.0× 1.8k 1.8× 240 0.6× 612 2.2× 273 1.0× 2 4.3k
Ami Levy‐Moonshine United States 5 2.2k 1.1× 1.9k 1.9× 256 0.6× 634 2.2× 280 1.0× 5 4.5k

Countries citing papers authored by Jochen Hecht

Since Specialization
Citations

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

Fields of papers citing papers by Jochen Hecht

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jochen Hecht

This figure shows the co-authorship network connecting the top 25 collaborators of Jochen Hecht. A scholar is included among the top collaborators of Jochen Hecht 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 Jochen Hecht. Jochen Hecht 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.
Esteller-Cucala, Paula, Lukas F. K. Kuderna, Claudia Fontsere, et al.. (2023). Y chromosome sequence and epigenomic reconstruction across human populations. Communications Biology. 6(1). 623–623. 2 indexed citations
2.
Hecht, Jochen, et al.. (2023). Epidemiology of healthcare-associated SARS-CoV-2 outbreaks in Germany between March 2020 and May 2022. Journal of Hospital Infection. 134. 108–120. 8 indexed citations
3.
Willis, Jesse R., Ester Saus, Susana Iraola‐Guzmán, et al.. (2022). Citizen-science reveals changes in the oral microbiome in Spain through age and lifestyle factors. npj Biofilms and Microbiomes. 8(1). 38–38. 43 indexed citations
4.
Brotons, Pedro, Iolanda Jordán, Quique Bassat, et al.. (2021). The Positive Rhinovirus/Enterovirus Detection and SARS-CoV-2 Persistence beyond the Acute Infection Phase: An Intra-Household Surveillance Study. Viruses. 13(8). 1598–1598. 16 indexed citations
5.
Gargano, Michael, Jochen Hecht, Jonas Ibn-Salem, et al.. (2019). Computational Processing and Quality Control of Hi-C, Capture Hi-C and Capture-C Data. Genes. 10(7). 548–548. 6 indexed citations
6.
Witte, Katrin, Karsten Jürchott, Jochen Hecht, et al.. (2019). Increased presence and differential molecular imprinting of transit amplifying cells in psoriasis. Journal of Molecular Medicine. 98(1). 111–122. 8 indexed citations
7.
Nienen, Mikalai, Ulrik Stervbo, Felix Mölder, et al.. (2019). The Role of Pre-existing Cross-Reactive Central Memory CD4 T-Cells in Vaccination With Previously Unseen Influenza Strains. Frontiers in Immunology. 10. 593–593. 22 indexed citations
8.
Orgeur, Mickael, Marvin Martens, Sonya Nassari, et al.. (2018). Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factors. Development. 145(7). 42 indexed citations
9.
Mackenroth, Luisa, Björn Fischer‐Zirnsak, Johannes Egerer, et al.. (2016). An overlapping phenotype of Osteogenesis imperfecta and Ehlers–Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing. American Journal of Medical Genetics Part A. 170(4). 1080–1085. 15 indexed citations
10.
Hecht, Jochen, et al.. (2016). Q-nexus: a comprehensive and efficient analysis pipeline designed for ChIP-nexus. BMC Genomics. 17(1). 873–873. 7 indexed citations
11.
Ibrahim, Daniel M., Naeimeh Tayebi, Alexej Knaus, et al.. (2015). A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. American Journal of Medical Genetics Part A. 170(3). 615–621. 15 indexed citations
12.
Krawitz, Peter, Ulrike Krüger, Sandra Appelt, et al.. (2014). Screening for single nucleotide variants, small indels and exon deletions with a next‐generation sequencing based gene panel approach for U sher syndrome. Molecular Genetics & Genomic Medicine. 2(5). 393–401. 22 indexed citations
13.
Neumann, Martín, Sandra Heesch, Cornelia Schlee, et al.. (2013). Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT3A mutations. Blood. 121(23). 4749–4752. 143 indexed citations
14.
Broecker, Felix, Michael Kube, Jochen Klumpp, et al.. (2013). Analysis of the Intestinal Microbiome of a Recovered <b><i>Clostridium difficile</i></b> Patient after Fecal Transplantation. Digestion. 88(4). 243–251. 29 indexed citations
15.
Krawitz, Peter, Yoshiko Murakami, Angelika Rieß, et al.. (2013). PGAP2 Mutations, Affecting the GPI-Anchor-Synthesis Pathway, Cause Hyperphosphatasia with Mental Retardation Syndrome. The American Journal of Human Genetics. 92(4). 584–589. 85 indexed citations
16.
Heinrich, Verena, Jens Stange, Thorsten Dickhaus, et al.. (2011). The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process. Nucleic Acids Research. 40(6). 2426–2431. 30 indexed citations
17.
Decker, Eva L., Sebastian Bender, Christian Rödelsperger, et al.. (2011). FGFR3 is a target of the homeobox transcription factor SHOX in limb development. Human Molecular Genetics. 20(8). 1524–1535. 40 indexed citations
18.
Villavicencio‐Lorini, Pablo, Pia Kuss, Julia Friedrich, et al.. (2010). Homeobox genes d11–d13 and a13 control mouse autopod cortical bone and joint formation. Journal of Clinical Investigation. 120(6). 1994–2004. 66 indexed citations
19.
Kuss, Pia, Pablo Villavicencio‐Lorini, Florian Witte, et al.. (2008). Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis. Journal of Clinical Investigation. 119(1). 146–56. 56 indexed citations
20.
Hecht, Jochen, Heiner Kuhl, Stefan A. Haas, et al.. (2006). Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep. BMC Genomics. 7(1). 172–172. 23 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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