Bettina Blaumeiser

4.1k total citations
40 papers, 650 citations indexed

About

Bettina Blaumeiser is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Urology. According to data from OpenAlex, Bettina Blaumeiser has authored 40 papers receiving a total of 650 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Pediatrics, Perinatology and Child Health, 16 papers in Genetics and 12 papers in Urology. Recurrent topics in Bettina Blaumeiser's work include Prenatal Screening and Diagnostics (16 papers), Hair Growth and Disorders (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Bettina Blaumeiser is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Hair Growth and Disorders (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Bettina Blaumeiser collaborates with scholars based in Belgium, Germany and United States. Bettina Blaumeiser's co-authors include Markus M. Nöthen, Regina C. Betz, S. Hanneken, Roland Kruse, Sibylle Eigelshoven, Gerhard Lutz, Silke Redler, J. De Weert, Julien Lambert and Yves Jacquemyn and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Bone and Mineral Research and Journal of Investigative Dermatology.

In The Last Decade

Bettina Blaumeiser

37 papers receiving 638 citations

Peers

Countries citing papers authored by Bettina Blaumeiser

Since Specialization

Citations

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

Fields of papers citing papers by Bettina Blaumeiser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bettina Blaumeiser

This figure shows the co-authorship network connecting the top 25 collaborators of Bettina Blaumeiser. A scholar is included among the top collaborators of Bettina Blaumeiser 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 Bettina Blaumeiser. Bettina Blaumeiser 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	The impact of confined placental mosaicism on prenatal cell-free DNA screening: Insights from a monocentric study of 99 cases 2024 ·Placenta ·Jessica Rosenblum, Bettina Blaumeiser, Katrien Janssens	1
2	Monocentric Study on the Performance of Noninvasive Prenatal Testing on Cell‐Free DNA for the Detection of Monosomy X 2024 ·Prenatal Diagnosis ·(unknown), Erik Fransén, Bettina Blaumeiser, Katrien Janssens	1
3	Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and Challenges 2023 ·Diagnostics ·(unknown), Marjan De Rademaeker, (unknown), Nele Boeckx, Bettina Blaumeiser, Katrien Janssens	8
4	Preconceptionele uitgebreide dragerschapsscreening: een genetische test voor koppels met een kinderwens 2023 ·Tijdschrift voor Geneeskunde ·(unknown), Hannah Verdin, Bettina Blaumeiser, (unknown), Paul Coucke, Sandra Janssens	0
5	Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles 2023 ·European Journal of Human Genetics ·Ilse Parijs, Nathalie Brison, Leen Vancoillie, Machteld Baetens, Bettina Blaumeiser, (unknown), Julie Désir, Boyan Dimitrov, Nathalie Fieremans, Katrien Janssens, Sandra Janssens, (unknown), Björn Menten, (unknown), (unknown), Ann Van Den Bogaert, Koenraad Devriendt, Kris Van Den Bogaert, Joris Vermeesch	2
6	Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approach 2019 ·Journal of Medical Ethics ·(unknown), Bettina Blaumeiser, Katrien Janssens, Patrick Loobuyck, Yves Jacquemyn	13
7	Parent-of-origin Effect in Alopecia Areata: A Large-scale Pedigree Study 2017 ·Acta Dermato Venereologica ·Silke Redler, (unknown), Bettina Blaumeiser, Natalie Garcia Bartels, Gerhard Lutz, (unknown), Roland Kruse, Hans Wolff, Markus Böhm, Ulrike Blume‐Peytavi, Tim Becker, Markus M. Nöthen, Regina C. Betz	2
8	Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies 2016 ·Genetics in Medicine ·Nathalie Brison, Kris Van Den Bogaert, Luc Dehaspe, (unknown), Katrien Janssens, Bettina Blaumeiser, Hilde Peeters, Hilde Van Esch, Griet Van Buggenhout, Annick Vogels, Thomy de Ravel, Eric Legius, Koenraad Devriendt, Joris Vermeesch	39
9	Investigation of selected cytokine genes suggests that IL2RA and the TNF / LTA locus are risk factors for severe alopecia areata 2012 ·British Journal of Dermatology ·Silke Redler, (unknown), F.F. Brockschmidt, Christine Herold, S. Hanneken, Sibylle Eigelshoven, Kathrin Giehl, Roland Kruse, Gerhard Lutz, Hans Wolff, Bettina Blaumeiser, Markus Böhm, Tim Becker, Markus M. Nöthen, Regina C. Betz	32
10	Follow-Up Study of the First Genome-Wide Association Scan in Alopecia Areata: IL13 and KIAA0350 as Susceptibility Loci Supported with Genome-Wide Significance 2012 ·Journal of Investigative Dermatology ·(unknown), Silke Redler, Felix F. Brockschmidt, Christine Herold, Sandra M. Pasternack, Natalie Garcia Bartels, S. Hanneken, Sibylle Eigelshoven, (unknown), Sandra Barth, Kathrin Giehl, Roland Kruse, Gerhard Lutz, Hans Wolff, Bettina Blaumeiser, Markus Böhm, Ulrike Blume‐Peytavi, Tim Becker, Markus M. Nöthen, Regina C. Betz	98
11	The TRAF1/C5 locus confers risk for familial and severe alopecia areata 2009 ·British Journal of Dermatology ·Silke Redler, F.F. Brockschmidt, (unknown), Kathrin Giehl, Christine Herold, Sibylle Eigelshoven, S. Hanneken, J. De Weert, Gerhard Lutz, Hans Wolff, Roland Kruse, Bettina Blaumeiser, Markus Böhm, Tim Becker, Markus M. Nöthen, Regina C. Betz	16
12	Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins 2008 ·American Journal of Medical Genetics Part A ·Bettina Blaumeiser, Barbara Oehl‐Jaschkowitz, Wiktor Borozdin, Jürgen Kohlhase	10
13	GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profiling 2007 ·Human Mutation ·Anna Caciotti, Maria Alice Donati, Elena Procopio, Mirella Filocamo, Wim J. Kleijer, Wim Wuyts, Bettina Blaumeiser, Alessandra d’Azzo, Lisa Simi, Claudio Orlando, Fiona McKenzie, Agata Fiumara, Enrico Zammarchi, Amelia Morrone	23
14	Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease 2007 ·Journal of Investigative Dermatology ·Regina C. Betz, (unknown), Antònia Flaquer, Silke Redler, S. Hanneken, Sibylle Eigelshoven, Anne-Katrin Kortüm, Thomas Tüting, Julien Lambert, J. De Weert, Axel M. Hillmer, Christine Schmael, Thomas F. Wienker, Roland Kruse, Gerhard Lutz, Bettina Blaumeiser, Markus M. Nöthen	83
15	Investigation of the functional variant c.‐169T > C of the Fc receptor‐like 3 (FCRL3) gene in alopecia areata 2006 ·International Journal of Immunogenetics ·Niklas Schäfer, Bettina Blaumeiser, Tim Becker, Yun Freudenberg‐Hua, S. Hanneken, Sibylle Eigelshoven, Christine Schmael, Jacques Lambert, J. De Weert, Roland Kruse, Markus M. Nöthen, Regina C. Betz	4
16	Investigation of the p.Ser278Arg polymorphism of the autoimmune regulator (AIRE) gene in alopecia areata 2006 ·Tissue Antigens ·(unknown), Bettina Blaumeiser, Tim Becker, Yun Freudenberg‐Hua, S. Hanneken, Sibylle Eigelshoven, (unknown), J. De Weert, Jacques Lambert, Roland Kruse, Markus M. Nöthen, Regina C. Betz	24
17	Familial aggregation of alopecia areata 2006 ·Journal of the American Academy of Dermatology ·Bettina Blaumeiser, (unknown), Rolf Fimmers, S. Hanneken, Sibylle Ritzmann, (unknown), Regina C. Betz, Thomas Ruzicka, Thomas F. Wienker, J. De Weert, Julien Lambert, Roland Kruse, Markus M. Nöthen	73
18	Adams–Oliver syndrome: clinical description of a four‐generation family and exclusion of five candidate genes 2005 ·Clinical Genetics ·Pieter Verdyck, Bettina Blaumeiser, Muriel Holder‐Espinasse, Wim Van Hul, Wim Wuyts	12
19	Prenatal diagnosis of Pfeiffer syndrome type II 2004 ·Prenatal Diagnosis ·Bettina Blaumeiser, (unknown), Wim Wuyts, Markus M. Nöthen	16
20	[Primary malignant melanoma of the female urethra]. 2000 ·PubMed ·Bettina Blaumeiser, Wiebren Tjalma, (unknown), (unknown), (unknown), P. Buytaert	6

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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