Christian Windpassinger

5.3k total citations
72 papers, 2.3k citations indexed

About

Christian Windpassinger is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Christian Windpassinger has authored 72 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 23 papers in Genetics and 18 papers in Cell Biology. Recurrent topics in Christian Windpassinger's work include Hereditary Neurological Disorders (10 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Christian Windpassinger is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Christian Windpassinger collaborates with scholars based in Austria, Canada and Pakistan. Christian Windpassinger's co-authors include Erwin Petek, Klaus Wagner, John B. Vincent, Peter M. Kroisel, Michaela Auer‐Grumbach, Abdul Noor, Stephen W. Scherer, Thomas Schwarzbraun, Roland Malli and Muzammil Ahmad Khan and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Environmental Science & Technology.

In The Last Decade

Christian Windpassinger

71 papers receiving 2.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Christian Windpassinger Austria	26	1.3k	500	451	415	207	72	2.3k
Bert van der Zwaag Netherlands	23	1.2k 0.9×	704 1.4×	372 0.8×	316 0.8×	200 1.0×	44	2.2k
Mari Auranen Finland	23	1.3k 1.0×	557 1.1×	343 0.8×	213 0.5×	362 1.7×	59	2.2k
Keling Zang United States	23	1.6k 1.2×	275 0.6×	1.7k 3.8×	464 1.1×	212 1.0×	27	3.8k
Christopher Grunseich United States	24	2.0k 1.5×	601 1.2×	639 1.4×	185 0.4×	193 0.9×	52	2.7k
Zhengmao Hu China	25	1000 0.8×	535 1.1×	430 1.0×	207 0.5×	295 1.4×	127	1.9k
Sakkubai Naidu United States	33	3.2k 2.5×	1.0k 2.1×	351 0.8×	381 0.9×	645 3.1×	80	4.4k
Kimia Kahrizi Iran	30	1.8k 1.4×	835 1.7×	203 0.5×	252 0.6×	162 0.8×	141	3.0k
Carlos Vicario‐Abejón Spain	30	1.3k 1.0×	218 0.4×	1.4k 3.1×	214 0.5×	148 0.7×	64	3.1k
Alexander Zimprich Austria	32	1.1k 0.9×	470 0.9×	1.4k 3.0×	330 0.8×	152 0.7×	76	3.3k

Countries citing papers authored by Christian Windpassinger

Since Specialization

Citations

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

Fields of papers citing papers by Christian Windpassinger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Windpassinger

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Windpassinger. A scholar is included among the top collaborators of Christian Windpassinger 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 Christian Windpassinger. Christian Windpassinger 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

Windpassinger, Christian, et al.. (2025). Functional Movement Disorder in Familial Ataxia: A Case Report of Monozygotic Twins. Movement Disorders Clinical Practice. 12(11). 1992–1994.

Guelly, Christian, Katrin Panzitt, Ulan Kozhamkulov, et al.. (2021). Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes. PeerJ. 9. e10711–e10711. 4 indexed citations

Scharnagl, Hubert, Marcus E. Kleber, Christian Windpassinger, et al.. (2019). Long- and short-term association of low-grade systemic inflammation with cardiovascular mortality in the LURIC study. Clinical Research in Cardiology. 109(3). 358–373. 17 indexed citations

Ahmed, Rizwan Raheem, Christian Windpassinger, Muhammad Salim, et al.. (2019). Genetic Study of Khyber-Pukhtunkhwa Resident Pakistani Families Presenting Primary Microcephaly With Intellectual Disability. Journal of the Pakistan Medical Association. 69(0). 1–1. 5 indexed citations

Feichtinger, René G., Michaela Brunner‐Krainz, Bader Alhaddad, et al.. (2017). Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative Medicine and Cellular Longevity. 2017(1). 7202589–7202589. 33 indexed citations

Bengesser, Susanne, Eva Z. Reininghaus, Nina Lackner, et al.. (2016). Is the molecular clock ticking differently in bipolar disorder? Methylation analysis of the clock gene ARNTL. The World Journal of Biological Psychiatry. 19(sup2). S21–S29. 32 indexed citations

Khan, Muzammil Ahmad, Sumitra Mohan, Muhammad Zubair, & Christian Windpassinger. (2016). Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndrome. BMC Medical Genetics. 17(1). 10–10. 12 indexed citations

Resch, Bernhard, et al.. (2015). Surfactant Protein B Deficiency Caused by Homozygous C248X Mutation—A Case Report and Review of the Literature. SHILAP Revista de lepidopterología. 5(1). e053–e059. 8 indexed citations

Rossmann, Christine, Christian Windpassinger, Daniela Brunner, et al.. (2014). Characterization of rat serum amyloid A4 (SAA4): A novel member of the SAA superfamily. Biochemical and Biophysical Research Communications. 450(4). 1643–1649. 10 indexed citations

10.

Khan, Muzammil Ahmad, Verena Rupp, Meritxell Orpinell, et al.. (2014). A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family. Human Molecular Genetics. 23(22). 5940–5949. 50 indexed citations

11.

Schreibmayer, Wolfgang, Benedikt Schoser, Gernot Desoyé, et al.. (2011). Four and a Half LIM Protein 1C (FHL1C): A Binding Partner for Voltage-Gated Potassium Channel Kv1.5. PLoS ONE. 6(10). e26524–e26524. 10 indexed citations

12.

Windpassinger, Christian, Judith A. Hudson, Bryan Lecky, et al.. (2011). Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 gene. European Journal of Human Genetics. 19(10). 1038–1044. 10 indexed citations

13.

Noor, Abdul, Christian Windpassinger, Irina Vitcu, et al.. (2009). Oligodontia Is Caused by Mutation in LTBP3, the Gene Encoding Latent TGF-β Binding Protein 3. The American Journal of Human Genetics. 84(4). 519–523. 65 indexed citations

14.

Schwarzbraun, Thomas, Reinhard Ullmann, Christian Windpassinger, et al.. (2006). Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development. Cytogenetic and Genome Research. 115(1). 84–89. 6 indexed citations

15.

Petek, Erwin, Thomas Schwarzbraun, Abdul Noor, et al.. (2006). Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome. Molecular Genetics and Genomics. 277(1). 71–81. 46 indexed citations

16.

Raedle, Jochen, Christian Windpassinger, Thomas Schwarzbraun, et al.. (2005). Phenotypic and molecular characterisation of a de novo 5q deletion that includes the APC gene. Journal of Human Genetics. 51(2). 141–146. 10 indexed citations

17.

Schwarzbraun, Thomas, John B. Vincent, Axel Schumacher, et al.. (2004). Cloning, genomic structure, and expression profiles of TULIP1 (GARNL1), a brain-expressed candidate gene for 14q13-linked neurological phenotypes, and its murine homologue. Genomics. 84(3). 577–586. 20 indexed citations

18.

Windpassinger, Christian, Klaus Wagner, Erwin Petek, Renate Fischer, & Michaela Auer‐Grumbach. (2003). Refinement of the "Silver syndrome locus" on chromosome 11q12-q14 in four families and exclusion of eight candidate genes. Human Genetics. 114(1). 99–109. 31 indexed citations

19.

Windpassinger, Christian, Peter M. Kroisel, Klaus Wagner, & Erwin Petek. (2002). The human γ-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression. Gene. 292(1-2). 25–31. 53 indexed citations

20.

Petek, Erwin, Christian Windpassinger, Joseph Cheung, et al.. (2001). Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome. The American Journal of Human Genetics. 68(4). 848–858. 130 indexed citations

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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