Markus Zweier

2.2k total citations
23 papers, 937 citations indexed

About

Markus Zweier is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Markus Zweier has authored 23 papers receiving a total of 937 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Markus Zweier's work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Markus Zweier is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Markus Zweier collaborates with scholars based in Switzerland, Germany and United States. Markus Zweier's co-authors include Anita Rauch, André Reis, Christiane Zweier, Arif B. Ekici, Emilia K. Bijlsma, Alfredo Orrico, Lilian Bomme Ousager, Merel A.W. Oortveld, Annette Schenck and Eiko K. de Jong and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Markus Zweier

22 papers receiving 923 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Markus Zweier Switzerland	12	582	547	138	85	80	23	937
Kimberly Chambert United States	10	509 0.9×	704 1.3×	104 0.8×	43 0.5×	102 1.3×	10	1.1k
Anneke T. Vulto-van Silfhout Netherlands	4	656 1.1×	959 1.8×	112 0.8×	69 0.8×	129 1.6×	4	1.3k
Zöe Powis United States	15	387 0.7×	562 1.0×	72 0.5×	60 0.7×	61 0.8×	34	873
Edwin J. Young Canada	13	538 0.9×	551 1.0×	69 0.5×	34 0.4×	90 1.1×	16	1.1k
Megan T. Cho United States	20	508 0.9×	462 0.8×	79 0.6×	27 0.3×	46 0.6×	27	838
Jean‐Baptiste Rivière Canada	18	591 1.0×	575 1.1×	101 0.7×	37 0.4×	145 1.8×	36	1.2k
Cheryl Shoubridge Australia	20	726 1.2×	748 1.4×	112 0.8×	17 0.2×	161 2.0×	49	1.3k
Sami S. Amr United States	18	460 0.8×	269 0.5×	71 0.5×	48 0.6×	21 0.3×	43	961
Rosangela Artuso Italy	14	447 0.8×	606 1.1×	210 1.5×	15 0.2×	32 0.4×	23	900
Yanjie Fan China	15	394 0.7×	304 0.6×	84 0.6×	42 0.5×	193 2.4×	48	792

Countries citing papers authored by Markus Zweier

Since Specialization

Citations

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

Fields of papers citing papers by Markus Zweier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markus Zweier

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

Brouwers, Sofie, Adriano Aguzzi, Thomas Fehr, et al.. (2024). Historic characteristics and mortality of patients in the Swiss Amyloidosis Registry. Swiss Medical Weekly. 154(2). 3485–3485. 2 indexed citations

Zanoni, Paolo, Katharina Steindl, Heinrich Sticht, et al.. (2023). The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohort. European Journal of Human Genetics. 31(7). 784–792. 6 indexed citations

Ivanovski, Ivan, Anaïs Begemann, Katharina Steindl, et al.. (2023). The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies. Molecular Genetics & Genomic Medicine. 11(5). e2148–e2148. 10 indexed citations

Ivanovski, Ivan, Angela Bahr, Markus Zweier, et al.. (2023). A very mild phenotype in six individuals of a three‐generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS‐related RASopathy distinct from Costello syndrome. American Journal of Medical Genetics Part A. 191(8). 2074–2082.

Bartsch, Oliver, Siren Berland, Ian Hayes, et al.. (2022). Further characterization of Borjeson‐Forssman‐Lehmann syndrome in females due to de novo variants in PHF6. Clinical Genetics. 102(3). 182–190. 3 indexed citations

Koller, Samuel, Elena Lang, Silke Feil, et al.. (2021). Genetic Analysis in a Swiss Cohort of Bilateral Congenital Cataract. JAMA Ophthalmology. 139(7). 691–691. 27 indexed citations

Oneda, Beatrice, Pietro Sirleto, Rosa Baldinger, et al.. (2020). Genome-wide non-invasive prenatal testing in single- and multiple-pregnancies at any risk: Identification of maternal polymorphisms to reduce the number of unnecessary invasive confirmation testing. European Journal of Obstetrics & Gynecology and Reproductive Biology. 252. 19–29. 9 indexed citations

Ruperti‐Repilado, Francisco Javier, Markus Zweier, Katharina Rentsch, et al.. (2019). Danger of Herbal Tea: A Case of Acute Cholestatic Hepatitis Due to Artemisia annua Tea. Frontiers in Medicine. 6. 221–221. 16 indexed citations

Begemann, Anaïs, Mario A. Acuña, Markus Zweier, et al.. (2019). Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes. Molecular Medicine. 25(1). 6–6. 39 indexed citations

10.

Azzarello‐Burri, Silvia, Katharina Steindl, Markus Zweier, et al.. (2019). Prevalence of genetic susceptibility for breast and ovarian cancer in a non-cancer related study population: secondary germline findings from a Swiss single centre cohort. Swiss Medical Weekly. 149(3334). w20092–w20092. 5 indexed citations

11.

Vasileiou, Georgia, Juliane Hoyer, Christian T. Thiel, et al.. (2019). Prenatal diagnosis of HNF1B ‐associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome?. Prenatal Diagnosis. 39(12). 1136–1147. 19 indexed citations

12.

Asadollahi, Reza, Markus Zweier, Raphael Schiffmann, et al.. (2017). Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation. European Journal of Medical Genetics. 60(9). 451–464. 32 indexed citations

13.

Zweier, Markus, et al.. (2016). The Buschke–Ollendorff syndrome: a case report of simultaneous osteo-cutaneous malformations in the hand. BMC Research Notes. 9(1). 294–294. 5 indexed citations

14.

Zweier, Markus, Heinrich Sticht, Christiane Zweier, et al.. (2013). Biallelic SEMA3A defects cause a novel type of syndromic short stature. American Journal of Medical Genetics Part A. 161(11). 2880–2889. 9 indexed citations

15.

Hoyer, Juliane, Arif B. Ekici, Sabine Endele, et al.. (2012). Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability. The American Journal of Human Genetics. 90(3). 565–572. 173 indexed citations

16.

Jamra, Rami Abou, Sigrun Wohlfart, Markus Zweier, et al.. (2011). Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity. European Journal of Human Genetics. 19(11). 1161–1166. 63 indexed citations

17.

Zweier, Markus & Anita Rauch. (2011). The MEF2C-Related and 5q14.3q15 Microdeletion Syndrome. Molecular Syndromology. 2(3-5). 164–170. 46 indexed citations

18.

Endele, Sabine, Silvia Azzarello‐Burri, Juliane Hoyer, et al.. (2011). In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of <b><i>SMARCA2</i></b> in Three Patients with Nicolaides-Baraitser Syndrome. Molecular Syndromology. 2(6). 237–244. 45 indexed citations

19.

Zweier, Markus, Anne Gregor, Christiane Zweier, et al.. (2010). Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Human Mutation. 31(6). 722–733. 114 indexed citations

20.

Zweier, Christiane, Eiko K. de Jong, Markus Zweier, et al.. (2009). CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila. The American Journal of Human Genetics. 85(5). 655–666. 244 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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