Martina Witsch‐Baumgartner

2.1k total citations
36 papers, 1.3k citations indexed

About

Martina Witsch‐Baumgartner is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Martina Witsch‐Baumgartner has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Surgery and 6 papers in Genetics. Recurrent topics in Martina Witsch‐Baumgartner's work include Cholesterol and Lipid Metabolism (14 papers), Peroxisome Proliferator-Activated Receptors (8 papers) and RNA and protein synthesis mechanisms (6 papers). Martina Witsch‐Baumgartner is often cited by papers focused on Cholesterol and Lipid Metabolism (14 papers), Peroxisome Proliferator-Activated Receptors (8 papers) and RNA and protein synthesis mechanisms (6 papers). Martina Witsch‐Baumgartner collaborates with scholars based in Austria, Germany and United Kingdom. Martina Witsch‐Baumgartner's co-authors include Gerd Utermann, Hartmut Glossmann, Barbara U. Fitzky, Fabian F. Moebius, Martin Erdel, Young‐Ki Paik, Judith Löffler‐Ragg, H. Zwierzina, Judith Löffler and Georg Mathias Sprinzl and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and British Journal of Cancer.

In The Last Decade

Martina Witsch‐Baumgartner

34 papers receiving 1.2k citations

Peers

Countries citing papers authored by Martina Witsch‐Baumgartner

Since Specialization

Citations

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

Fields of papers citing papers by Martina Witsch‐Baumgartner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martina Witsch‐Baumgartner. 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 Martina Witsch‐Baumgartner. The network helps show where Martina Witsch‐Baumgartner may publish in the future.

Co-authorship network of co-authors of Martina Witsch‐Baumgartner

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Retrospective identification of the first cord blood–transplanted severe aplastic anemia in a STAT1-associated chronic mucocutaneous candidiasis family: case report, review of literature and pathophysiologic background 2024 ·Frontiers in Immunology ·Franz‐Martin Fink, R. Höpfl, Martina Witsch‐Baumgartner, Gabriele Kropshofer, Sabine Martin, (unknown), Maximilian Heeg, Christina Peters, Johannes Zschocke, Oskar A. Haas	0
2	Amp(1q) and tetraploidy are commonly acquired chromosomal abnormalities in relapsed multiple myeloma 2022 ·European Journal Of Haematology ·(unknown), Emina Jukic, (unknown), Markus A. Keller, (unknown), (unknown), (unknown), Irmgard Verdorfer, (unknown), Martina Witsch‐Baumgartner, David Nachbaur, Wolfgang Willenbacher, Eberhard Gunsilius, Dominik Wolf‎, Johannes Zschocke, Normann Steiner	6
3	Identifying adult hypophosphatasia in the rheumatology unit 2022 ·Osteologie/Osteology ·(unknown), (unknown), (unknown), Judith Haschka, Katharina M. Roetzer, Gökhan Uyanık, Martina Witsch‐Baumgartner, Georg Schett, Jochen Zwerina, Roland Kocijan	1
4	Identifying adult hypophosphatasia in the rheumatology unit 2022 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), Judith Haschka, Katharina M. Roetzer, Gökhan Uyanık, (unknown), Martina Witsch‐Baumgartner, Georg Schett, Jochen Zwerina, Roland Kocijan	14
5	EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency 2020 ·European Journal of Human Genetics ·Sabina Baumgartner‐Parzer, Martina Witsch‐Baumgartner, Wolfgang Hoeppner	56
6	Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant 2020 ·Clinical Oral Investigations ·(unknown), Elisabeth Maurer, Martina Witsch‐Baumgartner, Robert Stigler, Johannes Zschocke, Adrian Lussi, Ines Kapferer‐Seebacher	4
7	Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern 2019 ·Birth Defects Research ·Katharina Schoner, Martina Witsch‐Baumgartner, (unknown), (unknown), R. Bald, Susanne Gerit Kircher, Annette Ramaswamy, Britta Kluge, (unknown), Ralf Schmitz, Bárbara Fritz, Johannes Zschocke, Franco Laccone, Helga Rehder	14
8	Influences of Pregnancy on Different Genetic Subtypes of Non-Dystrophic Myotonia and Periodic Paralysis 2016 ·Gynecologic and Obstetric Investigation ·Sabine Rudnik‐Schöneborn, Martina Witsch‐Baumgartner, Klaus Zerres	6
9	A recurrent germline mutation in the PIGA gene causes Simpson‐Golabi‐Behmel syndrome type 2 2015 ·American Journal of Medical Genetics Part A ·Christine Fauth, Katharina Steindl, Annick Toutain, Sandra A. Farrell, Martina Witsch‐Baumgartner, Daniela Karall, Pascal Joset, (unknown), Alessandra Baumer, Oliver Maier, Johannes Zschocke, Rosanna Weksberg, Christian R. Marshall, Anita Rauch	30
10	Genotype-based databases for variants causing rare diseases 2014 ·Gene ·(unknown), (unknown), Andrea Deutschmann, Anna Schossig, Christine Fauth, Johannes Zschocke, Martina Witsch‐Baumgartner	10
11	Single nucleotide polymorphism array analysis in men with idiopathic azoospermia or oligoasthenozoospermia syndrome 2013 ·Fertility and Sterility ·(unknown), P. H. Vogt, J. Zimmer, Martina Witsch‐Baumgartner, Christine Fauth, Johannes Zschocke, Germar‐Michael Pinggera, Dieter Kotzot	10
12	Maternal ABCA1 genotype is associated with severity of Smith–Lemli–Opitz syndrome and with viability of patients homozygous for null mutations 2012 ·European Journal of Human Genetics ·(unknown), Elisabeth Steichen‐Gersdorf, Barbara Kollerits, Johannes Zschocke, Martina Witsch‐Baumgartner	18
13	Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2 2012 ·European Journal of Human Genetics ·Erik‐Jan Kamsteeg, Wolfram Kreß, Claudio Catalli, Jens Michael Hertz, Martina Witsch‐Baumgartner, Michael F. Buckley, Baziel G.M. van Engelen, Marianne Schwartz, Hans Scheffer	100
14	Identification of the rare EGFR mutation p.G796S as somatic and germline mutation in white patients with squamous cell carcinoma of the head and neck 2008 ·Head & Neck ·Ilona Schwentner, Martina Witsch‐Baumgartner, Georg Mathias Sprinzl, Jens Krugmann, Alexandar Tzankov, Siegfried Jank, H. Zwierzina, Judith Löffler‐Ragg	25
15	Gefitinib-responsive EGFR-positive colorectal cancers have different proteome profiles from non-responsive cell lines 2005 ·European Journal of Cancer ·Judith Löffler‐Ragg, Sergej Skvortsov, Bettina Sarg, Ira Skvortsova, Martina Witsch‐Baumgartner, (unknown), Herbert Lindner, H. Zwierzina	26
16	Identification of 14 novel mutations inDHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of theDHCR7 mutational spectra in Spain and Italy 2005 ·Human Mutation ·Martina Witsch‐Baumgartner, Peter T. Clayton, Núria Clusellas, Dorothea Haas, Richard I. Kelley, Małgorzata Krajewska‐Walasek, Silvia Lechner, Massimiliano Rossi, Johannes Zschocke, Gerd Utermann	26
17	Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome 2004 ·Journal of Medical Genetics ·Martina Witsch‐Baumgartner, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	62
18	Molecular prenatal diagnosis of Smith–Lemli–Opitz syndrome is reliable and efficient 2002 ·Prenatal Diagnosis ·(unknown), Gerd Utermann, Martina Witsch‐Baumgartner	18
19	Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations 2001 ·European Journal of Human Genetics ·Martina Witsch‐Baumgartner, Elżbieta Ciara, Jürgen Löffler, (unknown), Udo Seedorf, John Burn, Gabriele Gillessen‐Kaesbach, G. F. Hoffmann, (unknown), Helen Mundy, Peter T. Clayton, (unknown), Małgorzata Krajewska‐Walasek, Gerd Utermann	53
20	Mutational Spectrum in the Δ7-Sterol Reductase Gene and Genotype-Phenotype Correlation in 84 Patients with Smith-Lemli-Opitz Syndrome 2000 ·The American Journal of Human Genetics ·Martina Witsch‐Baumgartner, Barbara U. Fitzky, M. Ogorelkova, H.G. Kraft, Fabian F. Moebius, Hartmut Glossmann, Udo Seedorf, Gabriele Gillessen‐Kaesbach, Georg F. Hoffmann, Peter T. Clayton, Richard I. Kelley, Gerd Utermann	154

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.

Explore authors with similar magnitude of impact