Heide Hellebrand

3.8k total citations
21 papers, 1.7k citations indexed

About

Heide Hellebrand is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Heide Hellebrand has authored 21 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Oncology. Recurrent topics in Heide Hellebrand's work include BRCA gene mutations in cancer (3 papers), DNA Repair Mechanisms (2 papers) and RNA regulation and disease (2 papers). Heide Hellebrand is often cited by papers focused on BRCA gene mutations in cancer (3 papers), DNA Repair Mechanisms (2 papers) and RNA regulation and disease (2 papers). Heide Hellebrand collaborates with scholars based in Germany, United Kingdom and United States. Heide Hellebrand's co-authors include Thomas Meitinger, Alfons Meindl, Eberhart Zrenner, Birgit Lorenz, Helene Achatz, A Meindl, Juliane Ramser, Astrid Golla, Eckart Apfelstedt-Sylla and Klaus Rüther and has published in prestigious journals such as Nature Genetics, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Heide Hellebrand

21 papers receiving 1.7k citations

Peers

Countries citing papers authored by Heide Hellebrand

Since Specialization

Citations

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

Fields of papers citing papers by Heide Hellebrand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heide Hellebrand

This figure shows the co-authorship network connecting the top 25 collaborators of Heide Hellebrand. A scholar is included among the top collaborators of Heide Hellebrand 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 Heide Hellebrand. Heide Hellebrand is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge 2020 ·Archives of Gynecology and Obstetrics ·Sabine Grill, Juliane Ramser, Heide Hellebrand, Nicole Pfarr, Melanie Boxberg, Christine Brambs, Nina Ditsch, Alfons Meindl, Eva Groß, Thomas Meitinger, Marion Kiechle, Anne S. Quante	6
2	The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer 2016 ·European Journal of Cancer Prevention ·Guido Neidhardt, Alexandra Becker, Jan Hauke, Judit Horváth, (unknown), Stefanie Heilmann‐Heimbach, Heide Hellebrand, Holger Thiele, Janine Altmüller, Peter Nürnberg, Alfons Meindl, Kerstin Rhiem, Britta Blümcke, Barbara Wappenschmidt, Rita K. Schmutzler, Eric Hahnen	7
3	Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer 2011 ·Human Mutation ·Heide Hellebrand, Christian Sutter, Ellen Honisch, Eva Groß, Barbara Wappenschmidt, Christian Schem, Helmut Deißler, Nina Ditsch, (unknown), Marion Kiechle, Claus R. Bartram, (unknown), Dieter Niederacher, Norbert Arnold, Alfons Meindl	36
4	KIF21A variant R954W in Familial or Sporadic Cases of CFEOM1 2009 ·European Journal of Ophthalmology ·Guenther Rudolph, Michael F. Nentwich, Heide Hellebrand, (unknown), (unknown), (unknown), Anselm Kampik, Alfons Meindl	5
5	Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy 2008 ·The American Journal of Human Genetics ·Juliane Ramser, Mary Ellen Ahearn, C Lenski, Kemal O. Yariz, Heide Hellebrand, Michael von Rhein, Robin D. Clark, Rita K. Schmutzler, Peter Lichtner, Eric P. Hoffman, Alfons Meindl, Lisa Baumbach‐Reardon	124
6	MLPA screening in theBRCA1gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases 2008 ·Human Mutation ·Stefanie Engert, Barbara Wappenschmidt, Beate Betz, Karin Kast, Michael Kutsche, Heide Hellebrand, Timm O. Goecke, Marion Kiechle, Dieter Niederacher, Rita K. Schmutzler, Alfons Meindl	74
7	Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker 2008 ·International Journal of Cancer ·Ariane Sadr‐Nabavi, Juliane Ramser, Jens Volkmann, J. Naehrig, Frank Wiesmann, Beate Betz, Heide Hellebrand, Stefanie Engert, Susanne Seitz, (unknown), Takako Sasaki, Norbert Arnold, Rita K. Schmutzler, Marion Kiechle, Dieter Niederacher, Nadia Harbeck, Edgar Dahl, Alfons Meindl	79
8	A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus: Limit of viability of Xp deletions in males 2006 ·American Journal of Medical Genetics Part A ·Volker O. Melichar, Sabine Guth, Heide Hellebrand, Alfons Meindl, Katharina von der Hardt, Cornelia Kraus, Udo Trautmann, Wolfgang Rascher, Anita Rauch, Martin Zenker	28
9	Persistent Hypogammaglobulinemia Following Mononucleosis in Boys Is Highly Suggestive of X-Linked Lymphoproliferative Disease—Report of Three Cases 2004 ·Journal of Clinical Immunology ·Boris Hügle, (unknown), Heide Hellebrand, Brian K. Adler, Michael Borte, Ulrich Sack, (unknown), (unknown), Jens Otto, A Meindl, Volker Schuster	9
10	High-throughput genotyping by DHPLC of the dihydropyrimidine dehydrogenase gene implicated in (fluoro)pyrimidine catabolism 2003 ·International Journal of Oncology ·Eva Groß, Katharina Seck, (unknown), (unknown), Heide Hellebrand, Adisorn Ratanaphan, Verena Lutz, Hubertus Stockinger, Marion Kiechle	22
11	Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 2002 ·European Journal of Human Genetics ·Astrid Golla, Annette Jansson, Juliane Ramser, Heide Hellebrand, R. Zahn, Thomas Meitinger, Bernd H. Belohradsky, Alfons Meindl	130
12	Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis 2002 ·Gene ·Attila Braun, Attila Aszódi, Heide Hellebrand, Alejandro Berna‐Erro, Reinhard Fässler, Oliver Brandau	34
13	Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP) 1999 ·Human Molecular Genetics ·Oliver Brandau, Volker Schuster, Michael Weiss, Heide Hellebrand, Franz Martin Fink, Alfons Kreczy, W Friedrich, Brigitte Strahm, Charlotte M. Niemeyer, B. H. Belohradsky, A Meindl	81
14	An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness 1998 ·Nature Genetics ·Tim M. Strom, Gerald Nyakatura, Eckart Apfelstedt-Sylla, Heide Hellebrand, Birgit Lorenz, Bernhard H. F. Weber, (unknown), (unknown), Klaus Rüther, Bernd Drescher, Christian Sauer, Eberhart Zrenner, Thomas Meitinger, André Rosenthal, Alfons Meindl	364
15	Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval. 1996 ·Genome Research ·Dirk Schindelhauer, Heide Hellebrand, (unknown), Ingrid Bader, Thomas Meitinger, M Wehnert, Mark Ross, A Meindl	24
16	A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) 1996 ·Nature Genetics ·A Meindl, Katherine L. Dry, Karin A. Herrmann, Forbes Manson, Alfredo Ciccodicola, (unknown), Maria Raquel Santos Carvalho, Helene Achatz, Heide Hellebrand, Alan Lennon, Carmela Migliaccio, Keith Porter, Eberhart Zrenner, Alan C. Bird, Marcelle Jay, Birgit Lorenz, B Wittwer, Michele D’Urso, Thomas Meitinger, Alan F. Wright	391
17	Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product 1996 ·Human Genetics ·Dirk Schindelhauer, Michael Weiss, Heide Hellebrand, Astrid Golla, Martin Hergersberg, Reinhard Seger, B. H. Belohradsky, A Meindl	75
18	Missense mutations in the NDP gene in patients with a less severe course of Norrie disease 1995 ·Human Molecular Genetics ·Alfons Meindl, (unknown), Helene Achatz, Heide Hellebrand, (unknown), Thomas Meitinger	53
19	A patient with an interstitial deletion in Xp22.3 locates the gene for X-linked recessive chondrodysplasia punctata to within a one megabase interval 1994 ·Human Genetics ·Albrecht Klink, (unknown), Heide Hellebrand, (unknown)	15
20	Norrie disease is caused by mutations in an extracellular protein resembling C–terminal globular domain of mucins 1992 ·Nature Genetics ·(unknown), Wolfgang Berger, Thomas Meitinger, Dorien van de Pol, Helene Achatz, (unknown), Martina Haasemann, Heide Hellebrand, Andreas Gal, Frans P.M. Cremers, Hans‐Hilger Ropers	130

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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