Karl Hackmann

3.1k citations

78 papers · 2.4k · h-index 28

Impact in

Genetics top 2%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Glioma Diagnosis and Treatment
Virology top 10%

Papers in

Genetics 60
- BRCA gene mutations in cancer 20
- Genomic variations and chromosomal abnormalities 18
- Genomics and Rare Diseases 17
- Genetics and Neurodevelopmental Disorders 10
- Genetic and Kidney Cyst Diseases 3
Virology 3
- HIV Research and Treatment 3

Co-authors: Evelin Schröck (42 shared papers)Andreas Rump (17 shared papers)Feng Qian (3 shared papers)Gregory George Germino (3 shared papers)Hangxue Xu (2 shared papers)Nataliya Di Donato (19 shared papers)Barbara Klink (12 shared papers)Sigrid Tinschert (8 shared papers)
Journals: European Journal of Medical Genetics (10 papers)Breast Cancer Research and Treatment (3 papers)European Journal of Human Genetics (3 papers)Journal of Medical Genetics (2 papers)Breast Cancer Research (2 papers)
Partner nations: Germany United States France

In The Last Decade

Karl Hackmann

76 papers receiving 2.4k citations

Peers

Countries citing papers authored by Karl Hackmann

Since Specialization

Citations

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

Fields of papers citing papers by Karl Hackmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Karl Hackmann, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Karl Hackmann Line = papers co-authored together Karl Hackmann links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 78 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Essential role of cleavage of Polycystin-1 at G protein-coupled receptor proteolytic site for kidney tubular structure Proceedings of the National Academy of Sciences ·Shengqiang Yu, Karl Hackmann, Jiangang Gao, Xiaobing He, Miguel Ángel García-González, Luís F. Menezes, Hangxue Xu, Gregory George Germino	2007	154
2	Gene panel testing of 5589 BRCA 1/2 ‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer Cancer Medicine ·Jan Hauke, Judit E. Horvath, Eva Groß, Andrea Gehrig, Ellen Honisch, Karl Hackmann, Gunnar Schmidt, Norbert Arnold	2018	137
3	Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification Human Mutation ·Michael T. Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lídia Feliubadaló, Cora M. Aalfs, Simona Agata	2019	121
4	Mutations in the Glycosylphosphatidylinositol Gene PIGL Cause CHIME Syndrome The American Journal of Human Genetics ·Bobby G. Ng, Karl Hackmann, Melanie A. Jones, Alexey M. Eroshkin, Ping He, Roy Wiliams, Shruti Bhide, Vincent Cantagrel	2012	111
5	Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 BMC Medical Genetics ·Anne Gregor, Beate Albrecht, Ingrid Bader, Emilia K. Bijlsma, Arif Bülent Ekici, Hartmut Engels, Karl Hackmann, Denise Horn	2011	107
6	Directed evolution of a recombinase that excises the provirus of most HIV-1 primary isolates with high specificity Nature Biotechnology ·Janet Karpinski, Ilona Hauber, Jan Chemnitz, Carola Schäfer, Maciej Paszkowski‐Rogacz, Debojyoti Chakraborty, Niklas Beschorner, Helga Hofmann-Sieber	2016	104
7	Characterization of cis-Autoproteolysis of Polycystin-1, the Product of Human Polycystic Kidney Disease 1 Gene Journal of Biological Chemistry ·Wen Wei, Karl Hackmann, Hangxue Xu, Gregory George Germino, Feng Qian	2007	96
8	BRIP1 loss-of-function mutations confer high risk for familial ovarian cancer, but not familial breast cancer Breast Cancer Research ·Nana Weber‐Lassalle, Jan Hauke, Juliane Ramser, Lisa Richters, Eva Groß, Britta Blümcke, Andrea Gehrig, Anne‐Karin Kahlert	2018	95
9	Comprehensive molecular characterization of multifocal glioblastoma proves its monoclonal origin and reveals novel insights into clonal evolution and heterogeneity of glioblastomas Neuro-Oncology ·Khalil Abou‐El‐Ardat, Michael Seifert, Kerstin Becker, Sophie Eisenreich, Karl Hackmann, Andreas Rump, Gerrit A. Meijer, Beatriz G. Carvalho	2016	94
10	Isogenic FUS-eGFP iPSC Reporter Lines Enable Quantification of FUS Stress Granule Pathology that Is Rescued by Drugs Inducing Autophagy Stem Cell Reports ·Lara Marrone, Ina Poser, Ian Casci, Julia Japtok, Peter Reinhardt, Antje Janosch, Cordula Andree, Hyun O. Lee	2018	88
11	Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer JAMA Oncology ·Guido Neidhardt, Jan Hauke, Juliane Ramser, Eva Groß, Andrea Gehrig, Clemens R. Müller, Anne‐Karin Kahlert, Karl Hackmann	2016	74
12	Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations European Journal of Human Genetics ·Nataliya Di Donato, Andreas Rump, Rainer Koenig, Vazken M. Der Kaloustian, Fahed Halal, Karl Hackmann, Gabriele Hahn, Evelin Schröck	2013	72
13	Characterization of the Binding Protein-Dependent Cellobiose and Cellotriose Transport System of the Cellulose Degrader Streptomyces reticuli Applied and Environmental Microbiology ·Andreas Schlösser, Jens Jantos, Karl Hackmann, Hildgund Schrempf	1999	70
14	Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt Journal of Medical Genetics ·Nataliya Di Donato, Teresa Neuhann, Anne‐Karin Kahlert, Barbara Klink, Karl Hackmann, Irmingard M. Neuhann, Jens Schallner, Ian A. Glass	2016	65
15	Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice PLoS Pathogens ·Ilona Hauber, Helga Hofmann-Sieber, Jan Chemnitz, Danilo Dubrau, Janet Chusainow, Rolf Stucka, Philip Hartjen, Axel Schambach	2013	53
16	PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans Journal of Medical Genetics ·Pauline Le Tanno, Marie Bidart, Véronique Satre, Radu Harbuz, Pierre F. Ray, Caroline Bosson, Klaus D. Dieterich, Sylvie Jaillard	2017	50
17	Homozygous loss of CHRNA7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia American Journal of Medical Genetics Part A ·Volker Endris, Karl Hackmann, Teresa Neuhann, Ute Grasshoff, Michael von Bonin, Ulrich Haug, Gabriele Hahn, Jens Schallner	2010	48
18	Clonal Evolution Including Partial Loss of Human Leukocyte Antigen Genes Favoring Extramedullary Acute Myeloid Leukemia Relapse After Matched Related Allogeneic Hematopoietic Stem Cell Transplantation Transplantation ·Friedrich Stölzel, Karl Hackmann, Friederike Kuithan, Brigitte Mohr, Monika Füssel, Uta Oelschlägel, Christian Thiede, Christoph Röllig	2012	48
19	Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers Annals of Oncology ·Arne Jahn, Andreas Rump, Thomas J. Widmann, Christoph Heining, Peter Horak, Barbara Hutter, Nagarajan Paramasivam, Sebastian Uhrig	2022	48
20	The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants International Journal of Cancer ·Stephanie Schubert, Jana Lisa van Luttikhuizen, Bernd Auber, Gunnar Schmidt, Winfried A. Hofmann, Judith Penkert, Colin Davenport, Ursula Hille‐Betz	2018	47

About Karl Hackmann

Karl Hackmann is a scholar working on Genetics, Virology, Pediatrics, Perinatology and Child Health, Neurology and Hematology, having authored 78 papers that have together received 2.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (20 papers), Genomic variations and chromosomal abnormalities (18 papers), Genomics and Rare Diseases (17 papers), Genetics and Neurodevelopmental Disorders (10 papers), HIV Research and Treatment (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genetic and Kidney Cyst Diseases (3 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Genetics (1.3k citations), Virology (57 citations), Genetics (101 citations), Molecular Biology (521 citations) and Developmental Neuroscience (22 citations). Karl Hackmann has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Evelin Schröck, Andreas Rump, Feng Qian, Gregory George Germino, Hangxue Xu, Nataliya Di Donato, Barbara Klink, Sigrid Tinschert, Andreas Schlösser and Hildgund Schrempf. Their work appears in journals such as European Journal of Medical Genetics, Breast Cancer Research and Treatment, European Journal of Human Genetics, Journal of Medical Genetics and Breast Cancer Research.

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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Karl Hackmann

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