Lisbeth Tranebjærg

11.9k citations

163 papers · 6.7k indexed · 1 hit paper · h-index 43

Impact in

Sensory Systems top 0.5%
- Hearing, Cochlea, Tinnitus, Genetics
Neurology top 1%
- Neuroinflammation and Neurodegeneration Mechanisms

Papers in

Sensory Systems 30
- Hearing, Cochlea, Tinnitus, Genetics 30
Genetics 61
- Genetics and Neurodevelopmental Disorders 26
- Genomic variations and chromosomal abnormalities 16

Co-authors: Nanna Dahl Rendtorff Claes Möller Herbert A. Lubs William J. Kimberling Niels Tommerup Martina C. Cornel Charles E. Schwartz Øivind Nilssen
Journals: European Journal of Human Genetics (19 papers)The American Journal of Human Genetics (7 papers)Journal of Medical Genetics (7 papers)Clinical Genetics (7 papers)Human Molecular Genetics (6 papers)
Partner nations: Denmark Norway United States

In The Last Decade

Lisbeth Tranebjærg

160 papers receiving 6.5k citations

Hit Papers

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Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype 2002 · 522 citations

Peers

Countries citing papers authored by Lisbeth Tranebjærg

Since Specialization

Citations

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

Fields of papers citing papers by Lisbeth Tranebjærg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Lisbeth Tranebjærg, 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 Lisbeth Tranebjærg Line = papers co-authored together Lisbeth Tranebjærg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Cascade counselling and testing. Recommendations of the European Society of Human Genetics European Journal of Human Genetics ·Guido de Wert, Carla van El, Angus Clarke, Christophe Cordier, Florence Fellmann, Maurizio Genuardi, Sabine Hentze, Hülya Kayserili, Milan Maçek, Jane Horan, Béla Melegh, Álvaro Mendes, Emmanuelle Rial‐Sebbag, Vigdís Stefánsdóttir, Lisbeth Tranebjærg, Fiona Ulph, Francesca Forzano	2025	0
2	Identification and analysis of deletion breakpoints in four Mohr-Tranebjærg syndrome (MTS) patients Scientific Reports ·Nanna Dahl Rendtorff, Hyunbae Chun Dongyun Yang, Marianne Lodahl, John Tolmie, Catherine McWilliam, Mads Bak, Niels Tommerup, Lusine Nazaryan‐Petersen, Henricus P. M. Kunst, Melanie Wong, Shelagh Joss, Valério Carelli, Lisbeth Tranebjærg	2022	3
3	Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome The American Journal of Human Genetics ·Acosta Sandra, Hanne Jensen, Jennifer J. Johnston, Emilio Di Maria, Katja Kloth, Н Г Суконна, Julie C. Sapp, Thomas N. Darling, Laryssa A. Huryn, Lisbeth Tranebjærg, Élisa Cinotti, Christian Kubisch, Eyvind Rødahl, Ove Bruland, Leslie G. Biesecker, Gunnar Houge, Cecilie Bredrup	2018	18
4	Partial USH2A deletions contribute to Usher syndrome in Denmark European Journal of Human Genetics ·Bae Kyoungjin, Nanna Dahl Rendtorff, Lionel Barber, Anders Albrechtsen, Mana M. Mehrjouy, Mads Bak, Niels Tommerup, Lisbeth Tranebjærg, Thomas Rosenberg, Hanne Jensen, Lisbeth Birk Møller	2015	8
5	Whole-genome sequencing in health care European Journal of Human Genetics ·Carla van El, Martina C. Cornel, Pascal Borry, Ros Hastings, Florence Fellmann, Shirley V. Hodgson, Heidi Howard, Anne Cambon‐Thomsen, Bartha Maria Knoppers, Hanne Meijers‐Heijboer, Hans Scheffer, Lisbeth Tranebjærg, Wybo Dondorp, Guido M. W. R. de Wert	2013	256
6	Mitochondrial 12S Ribosomal RNA A1555G Mutation Associated with Cardiomyopathy and Hearing Loss following High-Dose Chemotherapy and Repeated Aminoglycoside Exposure The Journal of Pediatrics ·van der Sluijs Jc, Lisbeth Tranebjærg, Tim Jensen, Henrik Hasle	2013	11
7	A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome Human Mutation ·Jorieke E. H. Bergman, Nicole Janssen, Almer M. van der Sloot, Hermien E. K. de Walle, Jeroen Schoots, Nanna Dahl Rendtorff, Lisbeth Tranebjærg, Lies H. Hoefsloot, Conny M.A. van Ravenswaaij‐Arts, Robert M.W. Hofstra	2012	50
8	Phenotype in 18 Danish subjects with genetically verified CHARGE syndrome Clinical Genetics ·Lucie-Patrizia Arndt, Amila Jeevan Wijayawardhana, Stense Farholt, Mikkel Bille, Lisbeth Tranebjærg, Ida Vogel, Sven Kreiborg	2012	30
9	Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene Clinical Genetics ·Chen Sun, Marijke Van Ghelue, Lisbeth Tranebjærg, Manuela Cuoghi, Ø. Nilssen, T. Torbergsen	2010	19
10	Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22 Hereditas ·Kristina Arheden, Umadevi Tantravahi, Niels Tommerup, Lisbeth Tranebjærg, Felix Mitelman	2008	0
11	Branchio-Oto-Renal Syndrome: Detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, sequencing and MLPA analyses European Journal of Human Genetics ·KIYOKO NONOYMA, Nanna Dahl Rendtorff, Klaus Kjaer, Hans Eiberg, Torsten Johnsen, Steen Gimsing, S J Rose, Δημήτριος Ζαμπούλης, G. B. Akram Khaleghei, Lisbeth Tranebjærg	2007	1
12	A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment European Journal of Human Genetics ·Nanna Dahl Rendtorff, Mei Zhu, Toril Fagerheim, Anthony J. Bent, MaryPat Jones, Tanya M. Teslovich, Elizabeth M. Gillanders, M. Michael Barmada, E. Teig, Jeffrey M. Trent, Karen H. Friderici, Dietrich Stephan, Lisbeth Tranebjærg	2006	54
13	Identification of a Novel EYA1 Splice-Site Mutation in a Danish Branchio-Oto-Renal Syndrome Family Genetic Testing ·胡珍斌, Zeynep Tümer, Niels Tommerup, Lisbeth Tranebjærg, Lars Allan Larsen	2004	7
14	Deoxyribonucleic Acid Contamination in Archival Human Temporal Bones: A Potentially Significant Problem Otology & Neurotology ·Michael J. McKenna, Arthur G. Kristiansen, Anke Tropitzsch, Lisbeth Tranebjærg, Saumil N. Merchant	2002	5
15	Two families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysis Scandinavian Audiology ·Michael Bille, A. F. López Sánchez, Lisbeth Tranebjærg, Toril Fagerheim, Amelia Putri	2001	3
16	A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation The American Journal of Human Genetics ·U. Uju, Lisbeth Tranebjærg, B. Quéfélec, Thomas Rosenberg, Claes Möller, Magdalena Beneyto, Michael D. Weston, Ahmad Saad Khan, Øivind Nilssen	2001	67
17	Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia European Journal of Human Genetics ·Yiwei Liu, Bjarne Udd, Vesa Juvonen, Peter M. Andersen, А. В. Рогозин, Weronika Lip, P. Sistonen, Гурбанмырадова Л., Lisbeth Tranebjærg, Carina Wallgren‐Pettersson, C. Vallo	2000	18
18	DFNA7 Advances in oto-rhino-laryngology ·Lisbeth Tranebjærg, Eugenio D’Amico, Rafia Farooq	2000	4
19	Localization to Xq22 and clinical update of a family with X-linked recessive mental retardation with progression sensorineural deafness, progressive tapeto-retinal degeneration and dystonia American Journal of Medical Genetics Part A ·Lisbeth Tranebjærg, Charles E. Schwartz, Vladimíra Michálková, David Barker, M. K. Andrews, J. Fernando Arena, Tobias Gedde‐Dahl, Margareta Mikkelsen, Svein Ivar Mellgren, Karen E. Anderson	1994	1
20	New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20q. Journal of Medical Genetics ·Michael B. Petersen, Lisbeth Tranebjærg, Niels Tommerup, Per Nygaard, Kartika Amanda	1987	44

About Lisbeth Tranebjærg

Lisbeth Tranebjærg is a scholar working on Sensory Systems, Genetics, Molecular Biology, Cell Biology and Otorhinolaryngology, having authored 163 papers that have together received 6.7k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (30 papers), Genetics and Neurodevelopmental Disorders (26 papers), Genomic variations and chromosomal abnormalities (16 papers), RNA regulation and disease (15 papers), Congenital heart defects research (14 papers), Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (12 papers) and Endoplasmic Reticulum Stress and Disease (11 papers). The work is most often cited by research in Sensory Systems (838 citations), Neurology (733 citations), Genetics (2.3k citations), Clinical Biochemistry (360 citations) and Molecular Biology (3.6k citations). Lisbeth Tranebjærg has collaborated with scholars based in Denmark, Norway and United States. Frequent co-authors include Nanna Dahl Rendtorff, Claes Möller, Herbert A. Lubs, William J. Kimberling, Niels Tommerup, Martina C. Cornel, Charles E. Schwartz, Øivind Nilssen, Thomas Rosenberg and Rolf Adolfsson. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics and Human Molecular Genetics.

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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