Holger Tönnies

3.6k citations

55 papers · 1.6k indexed · h-index 23

Molecular Biology top 10%
Genetics top 2%
Plant Science top 10%
Endocrinology, Diabetes and Metabolism top 10%
Pediatrics, Perinatology and Child Health top 10%

Co-authors: Heidemarie Neitzel Arpad von Moers Dirk Schnabel Frank K.H. van Landeghem Andreas von Deimling Annette Grüters Antony Lafferty S. Schwarz
Topics: Genomic variations and chromosomal abnormalities (23 papers)Chromosomal and Genetic Variations (13 papers)Prenatal Screening and Diagnostics (11 papers)
Cited by: Genetics Molecular Biology Endocrinology, Diabetes and Metabolism
Journals: Proceedings of the National Academy of Sciences Journal of Clinical Investigation Blood
Partner nations: Germany United States United Kingdom

In The Last Decade

Holger Tönnies

55 papers receiving 1.6k citations

Peers

Countries citing papers authored by Holger Tönnies

Since Specialization

Citations

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

Fields of papers citing papers by Holger Tönnies

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Holger Tönnies

This figure shows the co-authorship network connecting the top 25 collaborators of Holger Tönnies. A scholar is included among the top collaborators of Holger Tönnies 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 Holger Tönnies. Holger Tönnies 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	Predictive genetic testing, risk communication, and risk perception: an international expert meeting in Berlin, Germany 2013 ·Journal of Community Genetics ·Eva Fisher,(unknown),Holger Tönnies	5
2	Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption 2007 ·Genes Chromosomes and Cancer ·Stefan Meyer,William Fergusson,Anthony D. Whetton,Flávia Moreira-Leite,Stuart D Pepper,Crispin Miller,(unknown),Daniel J. White,Andrew Will,Tim Eden,Hideyuki Ikeda,Reinhard Ullmann,(unknown),(unknown),Eva Klopocki,Holger Tönnies	24
3	A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH 2007 ·European Journal of Pediatrics ·Eva Klopocki,Luitgard Graul‐Neumann,Ulrike Grieben,Holger Tönnies,Hans‐Hilger Ropers,Denise Horn,Stefan Mundlos,Reinhard Ullmann	43
4	Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure 2007 ·Orphanet Journal of Rare Diseases ·Bernd Gruhn,J. Seidel,F Zintl,Raymonda Varon,Holger Tönnies,Heidemarie Neitzel,Astrid Bechtold,Holger Hoehn,Detlev Schindler	47
5	CGH of microdissected Kaposi's sarcoma lesions reveals recurrent loss of chromosome Y in early and additional chromosomal changes in late tumour stages 2006 ·AIDS ·Pawan Pyakurel,(unknown),Esmeralda Castaños‐Vélez,Ephata Kaaya,Birger Christensson,Holger Tönnies,Peter Biberfeld,Thomas Heiden	17
6	Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8 2006 ·American Journal of Medical Genetics Part A ·Raymonda Varon,(unknown),Klaus Wagner,(unknown),(unknown),(unknown),Erwin Petek,Holger Tönnies,(unknown),Karl Sperling,Peter M. Kroisel	7
7	Symptoms of OTC deficiency but not DMD in a female carrier of an Xp21.1 deletion including the genes for dystrophin and OTC 2006 ·European Journal of Pediatrics ·Sibylle Jakubiczka,Thomas Bettecken,Klaus Mohnike,Reinhard Schneppenheim,Markus Stümm,Holger Tönnies,Marianne Volleth,Peter Wieacker	6
8	Complete Reversal of ABCG2-Depending Atypical Multidrug Resistance by RNA Interference in Human Carcinoma Cells 2006 ·Oligonucleotides ·(unknown),Franziska Rompe,Holger Tönnies,(unknown),Paweł Surowiak,A. Stege,Verena Materna,Hermann Lage	23
9	Ulnar–mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene 2006 ·European Journal of Human Genetics ·Eva Klopocki,Luitgard M. Neumann,Holger Tönnies,Hans‐Hilger Ropers,Stefan Mundlos,Reinhard Ullmann	34
10	Nuchal cystic hygroma in five fetuses from 1819 to 1826 in the Meckel‐anatomical collections at the University of Halle, Germany 2006 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),Karsten Stock,(unknown),Lennart Olsson,John M. Opitz,(unknown),Holger Tönnies	2
11	Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2‐q13 2006 ·Prenatal Diagnosis ·Marc Trimborn,Rolf‐Dieter Wegner,Holger Tönnies,Nanette Sarioglu,(unknown),Heidemarie Neitzel	9
12	Acrofacial dysostosis (AFD) with preaxial limb hypoplasia (Nager AFD) and club foot diagnosed in a fetus from 1812 in the anatomical collections at the University of Halle, Germany 2005 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),(unknown),Karsten Stock,(unknown),Lennart Olsson,(unknown),Holger Tönnies	3
13	Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the sonic hedgehog gene and the HLXB9 gene at 7q36.3 2004 ·American Journal of Medical Genetics Part A ·Denise Horn,Holger Tönnies,Heidemarie Neitzel,Dagmar Wahl,Georg Klaus Hinkel,Arpad von Moers,Oliver Bartsch	37
14	Genomic Aberrations and Survival in Cutaneous T Cell Lymphomas 2004 ·Journal of Investigative Dermatology ·Tanja Fischer,Sylke Gellrich,J. Marcus Muche,(unknown),Heike Audring,Heidemarie Neitzel,Peter Walden,Wolfram Sterry,Holger Tönnies	47
15	Genotype/phenotype analysis in a patient with pure and complete trisomy 12p 2004 ·American Journal of Medical Genetics Part A ·Walter Zumkeller,Marianne Volleth,Petra Muschke,Holger Tönnies,Anita Heller,Thomas Liehr,Peter Wieacker,Markus Stümm	22
16	Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition 2002 ·The American Journal of Human Genetics ·Heidemarie Neitzel,Luitgard M. Neumann,Detlev Schindler,(unknown),Holger Tönnies,Marc Trimborn,Alice Krebsová,(unknown),Karl Sperling	82
17	Familial interstitial 570 kbp deletion of the UBE3A gene region causing Angelman syndrome but not Prader‐Willi syndrome 2002 ·American Journal of Medical Genetics ·Joachim Bürger,Denise Horn,Holger Tönnies,Heidemarie Neitzel,André Reis	38
18	Johann Friedrich Meckel d. J. (1781–1833) und die moderne Teratologie 2002 ·Annals of Anatomy - Anatomischer Anzeiger ·(unknown),(unknown),(unknown),Holger Tönnies,(unknown)	6
19	Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency 2002 ·Journal of Clinical Investigation ·Heiko Krude,(unknown),Heike Biebermann,Arpad von Moers,Dirk Schnabel,(unknown),Holger Tönnies,Dagmar Weise,Antony Lafferty,S. Schwarz,(unknown),Andreas von Deimling,Frank K.H. van Landeghem,Roberto DiLauro,Annette Grüters	236
20	Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature 2001 ·European Journal of Pediatrics ·Jörg Müsebeck,Klaus Mohnike,(unknown),Holger Tönnies,Heidemarie Neitzel,Dirk Schnabel,(unknown),Peter Wieacker,Markus Stümm	21

About Holger Tönnies

Holger Tönnies is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 55 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Chromosomal and Genetic Variations (13 papers) and Prenatal Screening and Diagnostics (11 papers). The work is most often cited by research in Genetics (833 citations), Molecular Biology (927 citations) and Endocrinology, Diabetes and Metabolism (180 citations). Holger Tönnies has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Heidemarie Neitzel, Arpad von Moers, Dirk Schnabel, Frank K.H. van Landeghem, Andreas von Deimling, Annette Grüters, Antony Lafferty, S. Schwarz, Roberto DiLauro and Heiko Krude. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Blood.

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