Hans‐Dieter Rott

1.8k citations

19 papers · 841 indexed · h-index 14

Biomedical Engineering top 10%
Genetics top 10%
Molecular Biology
Radiology, Nuclear Medicine and Imaging top 10%
Surgery

Co-authors: Gail ter Haar Кazuo Maeda Marvin C. Ziskin Francis Duck Stanley B Barnett Karin Mayer Wolfgang G. Ballhausen Anita Rauch
Topics: Tuberous Sclerosis Complex Research (4 papers)Genetic and rare skin diseases. (4 papers)Ultrasound and Hyperthermia Applications (4 papers)
Cited by: Critical Care and Intensive Care Medicine Genetics Dermatology
Journals: The Lancet The American Journal of Human Genetics Journal of the American Academy of Dermatology
Partner nations: Germany Australia United States

In The Last Decade

Hans‐Dieter Rott

19 papers receiving 798 citations

Peers

Countries citing papers authored by Hans‐Dieter Rott

Since Specialization

Citations

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

Fields of papers citing papers by Hans‐Dieter Rott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hans‐Dieter Rott. 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 Hans‐Dieter Rott. The network helps show where Hans‐Dieter Rott may publish in the future.

Co-authorship network of co-authors of Hans‐Dieter Rott

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation 2003 ·The American Journal of Human Genetics ·Sarah A. Shoichet,Kirsten Hoffmann,Corinna Menzel,Udo Trautmann,Bettina A. Moser,Maria Hoeltzenbein,Bernard Échenne,M. W. Partington,Hans van Bokhoven,Claude Moraine,Jean‐Pierre Fryns,Jamel Chelly,Hans‐Dieter Rott,Hans‐Hilger Ropers,Vera M. Kalscheuer	65
2	Cyst‐like cerebral lesions in tuberous sclerosis 2002 ·American Journal of Medical Genetics ·Hans‐Dieter Rott,Beate Lemcke,Martin Zenker,W. Huk,Jürgen Horst,Karin Mayer	20
3	“Mowat-Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene 2002 ·American Journal of Medical Genetics ·Christiane Zweier,Beate Albrecht,Beate Mitulla,R. Behrens,(unknown),Gabriele Gillessen‐Kaesbach,Hans‐Dieter Rott,Anita Rauch	6
4	“Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene 2002 ·American Journal of Medical Genetics ·Christiane Zweier,Beate Albrecht,Beate Mitulla,R. Behrens,(unknown),(unknown),Hans‐Dieter Rott,Anita Rauch	89
5	International recommendations and guidelines for the safe use of diagnostic ultrasound in medicine 2000 ·Ultrasound in Medicine & Biology ·Stanley B Barnett,Gail ter Haar,Marvin C. Ziskin,Hans‐Dieter Rott,Francis Duck,Кazuo Maeda	275
6	Tuberous sclerosis type 1: Three novel mutations detected in exon 15 by a combination of HDA and TGGE 2000 ·Human Mutation ·(unknown),Karin Mayer,Hans‐Dieter Rott	2
7	Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences11Accession numbers and URLs for data in this article are as follows: Online Mendelian Inheritance in Man: http://www.ncbi.nlm.nih.gov/omim. For TSC1 (MIM 191100) and TSC2 (MIM 191092). The Human Gene Mutation Data Base, Cardiff (HGMD): http://www.uwcm.acuk/uwcm/mg. For TSC1 120735 and for TSC2 120466. TSC Variation Database: http://www.expmed.bwh.harvard.edu/projects/tsc_database. GenBank: http://www.ncbi.nlm.nih.gov/Genbank. For TSC2 cDNA X75621 and TSC2 complete genomic sequence AC005600. 2000 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Karin Mayer,Wolfgang G. Ballhausen,(unknown),Hans‐Dieter Rott	42
8	Mutation screening of the entire coding regions of theTSC1 and theTSC2 gene with the protein truncation test (PTT) identifies frequent splicing defects 1999 ·Human Mutation ·Karin Mayer,Wolfgang G. Ballhausen,Hans‐Dieter Rott	32
9	Safety of Ultrasonic Contrast Agents 1999 ·European Journal of Ultrasound ·Hans‐Dieter Rott	4
10	Extracutaneous analogies of Blaschko lines 1999 ·American Journal of Medical Genetics ·Hans‐Dieter Rott	22
11	Acoustic cavitation and capillary bleeding 1999 ·European Journal of Ultrasound ·Hans‐Dieter Rott	5
12	World Federation for Ultrasound in Medicine and Biology, task group report for safety committee of the WFUMB: conclusions and recommendations on thermal and non-thermal mechanisms for biological effects of ultrasound 1998 ·ePrints Soton (University of Southampton) ·Marvin C. Ziskin,Кazuo Maeda,Wesley L. Nyborg,Gail ter Haar,Hans‐Dieter Rott,Jens Bang,Edwin L. Carstensen,Michael Delius,Francis Duck,P. D. Edmonds,Leon A. Frizzell,(unknown),Masao Ide,T.G. Leighton,Douglas L. Miller,R C Preston,(unknown),(unknown),(unknown),(unknown)	17
13	The sensitivity of biological tissue to ultrasound 1997 ·Ultrasound in Medicine & Biology ·(unknown),Hans‐Dieter Rott,Gail ter Haar,Marvin C. Ziskin,Кazuo Maeda	133
14	Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion 1996 ·Human Genetics ·Thomas Liehr,Bernd Rautenstrauß,H. Grehl,(unknown),Arif B. Ekici,Anita Rauch,Hans‐Dieter Rott	33
15	Chromosomal mosaicism in two patients with epidermal verrucous nevus 1994 ·Journal of the American Academy of Dermatology ·(unknown),(unknown),(unknown),Uwe Claussen,O. P. Hornstein,Hans‐Dieter Rott	17
16	Hydantoin syndrome with holoprosencephaly: A possible rare teratogenic effect 1993 ·Teratology ·Dieter Kotzot,Josef Weigl,W. Huk,Hans‐Dieter Rott	13
17	Hypomelanosis of Ito and chromosomal mosaicism in fibroblasts. 1986 ·PubMed ·Hans‐Dieter Rott,(unknown),Eckart Haneke,I. T. Thomas,Jaime L. Frías	35
18	HYPOMELANOSIS OF ITO AND CHROMOSOMAL MOSAICISM IN FIBROBLASTS 1986 ·The Lancet ·Hans‐Dieter Rott,(unknown),Eckart Haneke,I. T. Thomas,Jaime L. Frías	30
19	DUCHENNE MUSCULAR DYSTROPHY: CARRIER DETECTION BY ULTRASOUND AND COMPUTERISED TOMOGRAPHY 1984 ·The Lancet ·Hans‐Dieter Rott,(unknown),(unknown)	1

About Hans‐Dieter Rott

Hans‐Dieter Rott is a scholar working on Developmental Biology, Genetics and Critical Care and Intensive Care Medicine, having authored 19 papers that have together received 841 indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (4 papers), Genetic and rare skin diseases. (4 papers) and Ultrasound and Hyperthermia Applications (4 papers). The work is most often cited by research in Critical Care and Intensive Care Medicine (39 citations), Genetics (209 citations) and Dermatology (56 citations). Hans‐Dieter Rott has collaborated with scholars based in Germany, Australia and United States. Frequent co-authors include Gail ter Haar, Кazuo Maeda, Marvin C. Ziskin, Francis Duck, Stanley B Barnett, Karin Mayer, Wolfgang G. Ballhausen, Anita Rauch, Jaime L. Frías and Eckart Haneke. Their work appears in journals such as The Lancet, The American Journal of Human Genetics and Journal of the American Academy of Dermatology.

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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