Karl Hackmann

3.1k citations

54 papers · 1.3k indexed · h-index 19

Genetics top 5%
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 8
- BRCA gene mutations in cancer 7
- Genetic Syndromes and Imprinting 4
- Congenital Ear and Nasal Anomalies 4
- Genomics and Rare Diseases 3
Genetics top 10%
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 8
- BRCA gene mutations in cancer 7
- Genetic Syndromes and Imprinting 4
- Congenital Ear and Nasal Anomalies 4
- Genomics and Rare Diseases 3
Virology top 10%
Molecular Biology top 10%
- CRISPR and Genetic Engineering 7
- Congenital heart defects research 6
Pathology and Forensic Medicine top 10%

Co-authors: Evelin Schröck Feng Qian Gregory G. Germino Hangxue Xu Andreas Rump Nataliya Di Donato Barbara Klink Hildgund Schrempf
Cited by: Genetics Virology
Journals: European Journal of Medical Genetics (10 papers)Breast Cancer Research and Treatment (3 papers)European Journal of Human Genetics (2 papers)
Partner nations: Germany United States France

In The Last Decade

Karl Hackmann

53 papers receiving 1.2k 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-authorship network

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

#	Work
1	Long-read genome and RNA sequencing resolve a pathogenic intronic germline LINE-1 insertion in APC npj Genomic Medicine ·K.J. Park,Karhleen K. Bucholz,Vitor Rafael Monteiro De Lima,R. de Groot,Werner Eck,Thomas J. Widmann,石天宝,Karl Hackmann,Sylke Winkler,Daniela Richter,Isabel Spier,Stefan Aretz,Daniela E. Aust,Joseph Porrmann,Doreen William,Evelin Schröck,Hanno Glimm,Arne Jahn	2025	1
2	PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome European Journal of Medical Genetics ·A. S. Athigiri Arulalan,Andreas Rump,Andreas Tzschach,Alexander Czech,Evelin Schröck,Karl Hackmann,Nataliya Di Donato	2018	7
3	Novel truncating PPM1D mutation in a patient with intellectual disability European Journal of Medical Genetics ·Joseph Porrmann,Andreas Rump,Karl Hackmann,Nataliya Di Donato,Anne‐Karin Kahlert,Johannes Maximilian Wagner,Arne Jahn,Muhammad Wasiq Ejaz .,Y. P. Chen,Evelin Schröck,Andreas Tzschach,Laura Gieldon	2018	6
4	Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion Ophthalmic Genetics ·Seraina Kunz,Joseph Porrmann,Martin Smitka,Muhammad Wasiq Ejaz .,Evelin Schröck,Karl Hackmann,Robert Herber,Frederik Raiskup,Andreas Tzschach	2018	1
5	Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity Breast Cancer Research ·Judith Penkert,Gunnar Schmidt,Winfried Hofmann,Stephanie Schubert,Maximilian Schieck,Bernd Auber,Tim Ripperger,Karl Hackmann,Marc Sturm,Holger Prokisch,Bernhard Kr,고성재,Thomas Illig,Brigitte Schlegelberger,Doris Steinemann	2018	6
6	Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome Breast Cancer Research and Treatment ·Paola Concolino,M Kamegawa,Karl Hackmann,Ida Paris,Angelo Minucci,Elisa De Paolis,Giovanni Scambia,Cecilia Zuppi,Evelin Schröck,Ettore Capoluongo	2017	15
7	Identification and Characterization of a New BRCA2 Rearrangement in an Italian Family with Hereditary Breast and Ovarian Cancer Syndrome Molecular Diagnosis & Therapy ·Paola Concolino,M Kamegawa,Karl Hackmann,Angelo Minucci,Giovanni Luca Scaglione,Maria De Bonis,Alessandra Costella,Cecilia Zuppi,Evelin Schröck,Ettore Capoluongo	2017	12
8	Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH Breast Cancer Research and Treatment ·Karl Hackmann,jafar babapour,T. Kavitha,Anne‐Karin Kahlert,Luisa Mackenroth,Barbara Klink,Nataliya Di Donato,Andreas Tzschach,Karin Kast,Pauline Wimberger,Evelin Schröck,Andreas Rump	2016	12
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,S. M. SZE,Matthias Lehmann,Karl Hackmann,Andreas Rump,Gerrit A. Meijer,Beatriz Carvalho,Achim Temme,Gabriele Schackert,Evelin Schröck,Dietmar Krex,Barbara Klink	2016	78
10	Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities? American Journal of Medical Genetics Part A ·Karl Hackmann,Andreas Rump,Stefan A. Haas,Johannes R. Lemke,Jean‐Pierre Fryns,Andreas Tzschach,Dagmar Wieczorek,Beate Albrecht,Alma Kuechler,Tim Ripperger,W Lafarge Maxime,Konrad Oexle,Sigrid Tinschert,Evelin Schröck,Vera M. Kalscheuer,Nataliya Di Donato	2015	8
11	Distinct phenotype of PHF6 deletions in females European Journal of Medical Genetics ·Nataliya Di Donato,Е. В. Речкина,Louis C. Bock,C. Le Caignec,Barbara Klink,Cornelia Kraus,Evelin Schröck,Karl Hackmann	2014	15
12	Interstitial deletion 1p36.32 in two brothers with a distinct phenotype – Overgrowth, macrocephaly and nearly normal intellectual function European Journal of Medical Genetics ·Nataliya Di Donato,Barbara Klink,Gabriele Hahn,Evelin Schröck,Karl Hackmann	2014	3
13	Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3 American Journal of Medical Genetics Part A ·Karl Hackmann,Yasin Kara,Jens Schallner,María Guadalupe Rodríguez-Carrillo,Lele Li,Evelin Schröck,Andreas Rump,Christine Fauth,Sigrid Tinschert,Konrad Oexle	2013	13
14	Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice PLoS Pathogens ·Ilona Hauber,Karima Chgoura,Jan Chemnitz,Shakil Mirza,Janet Chusainow,Rolf Stucka,Philip Hartjen,Axel Schambach,Patrick Ziegler,Karl Hackmann,Evelin Schröck,Udo Schumacher,Christoph Lindner,Adam Grundhoff,Christopher Baum,Markus G. Manz,Frank Buchholz,Joachim Hauber	2013	47
15	Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection Oncogenesis ·Martin Michaelis,Stefan Barth,Rainer Breitling,Jochen Bruch,Daniela Steinberger,Florian Rothweiler,Karl Hackmann,Evelin Schröck,H. W. Doerr,Darren K. Griffin,Jindřich Činátl	2012	5
16	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,Beatrice Gruendler,Brigitte Mohr,Monika Füssel,Uta Oelschlägel,Christian Thiede,Christoph Röllig,Uwe Platzbecker,Johannes Schetelig,Thomas Illmer,Markus Schaich,Barbara Seliger,Arndt Hartmann,Gustavo Baretton,Christian Zietz,Gerhard Ehninger,Evelin Schröck,Martin Bornhäuser	2012	37
17	Partial deletion of GLRB and GRIA2 in a patient with intellectual disability European Journal of Human Genetics ·Karl Hackmann,成都铁路局货运事业部,Lele Li,Maja von der Hagen,Barbara Klink,Evelin Schröck,Andreas Rump,Nataliya Di Donato	2012	19
18	Macrocephaly, obesity, mental (intellectual) disability, and ocular abnormalities: Alternative definition and further delineation of MOMO syndrome American Journal of Medical Genetics Part A ·Nataliya Di Donato,(unknown),Karl Hackmann,Andreas Rump,Angela Huebner,Maja von der Hagen,Gabriele Hahn,Evelin Schröck,Sigrid Tinschert	2012	6
19	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,Klaus Piontek,Miguel A. García-González,Luís F. Menezes,Hangxue Xu,Gregory G. Germino,Jianping Zuo,Feng Qian	2007	136
20	Characterization of cis-Autoproteolysis of Polycystin-1, the Product of Human Polycystic Kidney Disease 1 Gene Journal of Biological Chemistry ·Muhammad Try Putra,Karl Hackmann,Hangxue Xu,Gregory G. Germino,Feng Qian	2007	86

About Karl Hackmann

Karl Hackmann is a scholar working on Genetics, Genetics and Virology, having authored 54 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (8 papers), BRCA gene mutations in cancer (7 papers), CRISPR and Genetic Engineering (7 papers), Congenital heart defects research (6 papers), Genetic Syndromes and Imprinting (4 papers), Congenital Ear and Nasal Anomalies (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (614 citations), Genetics (128 citations) and Virology (52 citations). Karl Hackmann has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Evelin Schröck, Feng Qian, Gregory G. Germino, Hangxue Xu, Andreas Rump, Nataliya Di Donato, Barbara Klink, Hildgund Schrempf, Andreas Schlösser and Sigrid Tinschert. Their work appears in journals such as European Journal of Medical Genetics, Breast Cancer Research and Treatment, European Journal of Human Genetics, Molecular Diagnosis & Therapy and PLoS ONE.

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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