Thomas Schwarzbraun

1.3k total citations
26 papers, 852 citations indexed

About

Thomas Schwarzbraun is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Thomas Schwarzbraun has authored 26 papers receiving a total of 852 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 4 papers in Epidemiology. Recurrent topics in Thomas Schwarzbraun's work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Chromatin Dynamics (4 papers). Thomas Schwarzbraun is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Chromatin Dynamics (4 papers). Thomas Schwarzbraun collaborates with scholars based in Austria, Germany and Canada. Thomas Schwarzbraun's co-authors include Michael R. Speicher, Jochen B. Geigl, Anna C. Obenauf, Erwin Petek, Lily Wang, Erich A. Nigg, Christian Windpassinger, John B. Vincent, Klaus Wagner and Abdul Noor and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Trends in Genetics.

In The Last Decade

Thomas Schwarzbraun

26 papers receiving 830 citations

Peers

Countries citing papers authored by Thomas Schwarzbraun

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Schwarzbraun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Schwarzbraun

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Schwarzbraun. A scholar is included among the top collaborators of Thomas Schwarzbraun 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 Thomas Schwarzbraun. Thomas Schwarzbraun 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	Cardio-pathogenic variants in unexplained intrauterine fetal death: a retrospective pilot study 2021 ·Scientific Reports ·(unknown), Martina Kollmann, (unknown), Gregor Hoermann, Peter Husslein, Ingrid Lafer, Erwin Petek, Thomas Schwarzbraun	6
2	Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families 2014 ·Neurogenetics ·(unknown), Katharina M. Roetzer, Abdul Noor, Anath C. Lionel, (unknown), Thomas Schwarzbraun, (unknown), Anna Mikhailov, Christian R. Marshall, Christian Windpassinger, Erwin Petek, Stephen W. Scherer, Wolfgang Kaschnitz, John B. Vincent	90
3	Re‐alignment‐procedures for Skeletal Dysplasia in Three Patients with Genetically Diverse Syndromes 2013 ·Orthopaedic Surgery ·Ali Al Kaissi, Rudolf Ganger, Katharina M. Roetzer, Thomas Schwarzbraun, Klaus Klaushofer, Franz Grill	3
4	Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation 2011 ·European Journal of Paediatric Neurology ·(unknown), Arndt Rolfs, Thomas Schwarzbraun, Christine Klein, Finbar O’Callaghan	15
5	MODY type 2 in Greig cephalopolysyndactyly syndrome (GCPS) as part of a contiguous gene deletion syndrome 2011 ·American Journal of Medical Genetics Part A ·Amnon Zung, Erwin Petek, Bruria Ben‐Zeev, Thomas Schwarzbraun, (unknown)	15
6	Androgen receptor expression in breast cancer patients tested for BRCA1 and BRCA2 mutations 2010 ·Histopathology ·Gunda Pristauz, Edgar Petru, Elvira Stacher, Jochen B. Geigl, Thomas Schwarzbraun, Oleksiy Tsybrovskyy, Raimund Winter, Farid Moinfar	25
7	Further evidence for the pathogenicity of 15q24 microduplications distal to the minimal critical regions 2010 ·American Journal of Medical Genetics Part A ·Katharina M. Roetzer, Thomas Schwarzbraun, Anna C. Obenauf, Erwin Hauser, Michael R. Speicher	9
8	The G protein-coupled receptor associated sorting protein GASP-1 regulates the signaling and trafficking of the viral chemokine receptor US28 2010 ·Traffic ·(unknown), (unknown), Dawn Thompson, Henry F. Vischer, Gerald P. Parzmair, (unknown), Wolfgang Platzer, Thomas Schwarzbraun, Helmut Schaider, Martine J. Smit, Lene Martini, Jennifer L. Whistler, Maria Waldhoer	6
9	Altered bone matrix mineralization in a patient with Rett syndrome 2010 ·Bone ·Jochen G. Hofstaetter, Katharina M. Roetzer, P Krepler, (unknown), Thomas Schwarzbraun, Klaus Klaushofer, Paul Roschger	8
10	Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations 2009 ·European Journal of Human Genetics ·Gábriel Miltenberger-Miltényi, Thomas Schwarzbraun, Wolfgang N. Löscher, Julia Wanschitz, Christian Windpassinger, Hans‐Christoph Duba, Rainer Seidl, (unknown), Helga Weirich‐Schwaiger, Heinz Zoller, Gerd Utermann, Michaela Auer‐Grumbach, Andreas Janecke	16
11	Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close toSH3TC2,ADRB2, andHTR4on 5q, and within the desmocollin gene cluster on 18q 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·John B. Vincent, Abdul Noor, Christian Windpassinger, Peter J. Gianakopoulos, Thomas Schwarzbraun, Simon E. Alfred, (unknown), Stephen W. Scherer, Wendy Roberts, Klaus Wagner, Peter M. Kroisel, Erwin Petek	11
12	Defining ‘chromosomal instability’ 2008 ·Trends in Genetics ·Jochen B. Geigl, Anna C. Obenauf, Thomas Schwarzbraun, Michael R. Speicher	254
13	Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the myelin transcription factor 1 gene (MYT1) 2008 ·Clinical Genetics ·(unknown), Erwin Petek, Thomas Schwarzbraun, (unknown), Barbara Plecko	21
14	An X-Linked Myopathy with Postural Muscle Atrophy and Generalized Hypertrophy, Termed XMPMA, Is Caused by Mutations in FHL1 2008 ·The American Journal of Human Genetics ·Christian Windpassinger, Benedikt Schoser, Volker Straub, Sonja Hochmeister, Abdul Noor, Birgit Lohberger, Natalie Farra, Erwin Petek, Thomas Schwarzbraun, (unknown), Wolfgang N. Löscher, Klaus Wagner, Hanns Lochmüller, John B. Vincent, Stefan Quasthoff	105
15	Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenation 2007 ·Chromosoma ·Lily Wang, Thomas Schwarzbraun, Michael R. Speicher, Erich A. Nigg	101
16	A new 3p interstitial deletion including the entire MITF gene causes a variation of Tietz/Waardenburg type IIA syndromes 2007 ·American Journal of Medical Genetics Part A ·Thomas Schwarzbraun, (unknown), Gabriele Gillessen‐Kaesbach, (unknown), Karl‐Heinz Preisegger, Christian Windpassinger, Klaus Wagner, Erwin Petek, Peter M. Kroisel	13
17	Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development 2006 ·Cytogenetic and Genome Research ·Thomas Schwarzbraun, Reinhard Ullmann, (unknown), (unknown), (unknown), Christian Windpassinger, Kay‐Uwe Wagner, Peter M. Kroisel, Erwin Petek	6
18	Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome 2006 ·Molecular Genetics and Genomics ·Erwin Petek, Thomas Schwarzbraun, Abdul Noor, Megha Patel, Kazuhiko Nakabayashi, Sanaa Choufani, Christian Windpassinger, M. Stamenković, Mary M. Robertson, H.N. Aschauer, Hugh Gurling, Peter M. Kroisel, Klaus Wagner, Stephen W. Scherer, John B. Vincent	46
19	Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene 2005 ·Journal of Human Genetics ·(unknown), Jochen Raedle, Christian Windpassinger, Thomas Schwarzbraun, Peter M. Kroisel, Klaus Wagner, Erwin Petek	10
20	Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue 2004 ·Genomics ·Thomas Schwarzbraun, John B. Vincent, Axel Schumacher, Daniel H. Geschwind, João Ricardo Mendes de Oliveira, Christian Windpassinger, (unknown), (unknown), Peter M. Kroisel, Klaus Wagner, Erwin Petek	20

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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