Birgitta Gläser

546 total citations
21 papers, 422 citations indexed

About

Birgitta Gläser is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Birgitta Gläser has authored 21 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Plant Science. Recurrent topics in Birgitta Gläser's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genomics and Chromatin Dynamics (5 papers) and Chromosomal and Genetic Variations (3 papers). Birgitta Gläser is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genomics and Chromatin Dynamics (5 papers) and Chromosomal and Genetic Variations (3 papers). Birgitta Gläser collaborates with scholars based in Germany, United Kingdom and Poland. Birgitta Gläser's co-authors include W. Schempp, Barbara Zoll, Roland Toder, Jürgen Kunz, Susanne Frank, Peter Burfeind, Bastian Pasche, Heidrun Ellinger‐Ziegelbauer, C Dreyer and Gudrun Rappold and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Biochemical and Biophysical Research Communications and International Journal of Molecular Sciences.

In The Last Decade

Birgitta Gläser

21 papers receiving 415 citations

Peers

Countries citing papers authored by Birgitta Gläser

Since Specialization

Citations

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

Fields of papers citing papers by Birgitta Gläser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgitta Gläser

This figure shows the co-authorship network connecting the top 25 collaborators of Birgitta Gläser. A scholar is included among the top collaborators of Birgitta Gläser 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 Birgitta Gläser. Birgitta Gläser 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	CRISPR-Cas12a for Highly Efficient and Marker-Free Targeted Integration in Human Pluripotent Stem Cells 2024 ·International Journal of Molecular Sciences ·(unknown), Jamal Alzubi, Manuel Rhiel, (unknown), (unknown), (unknown), (unknown), (unknown), Valentina Pennucci, Birgitta Gläser, Judith Fischer, Axel Schambach, Thomas Moritz, Nico Lachmann, Tatjana I. Cornu, Claudio Mussolino, Richard Schäfer, Toni Cathomen	3
2	Obsessive–compulsive symptoms and 15q11.2q13.1 duplication syndrome 2023 ·European Neuropsychopharmacology ·(unknown), Alexander Maier, (unknown), Kimon Runge, Kathrin Nickel, Ludger Tebartz van Elst, Miriam A. Schiele, Katharina Domschke, Birgitta Gläser, Andreas Tzschach, Katalin Komlósi, Dominique Endres	1
3	Marfan Syndrome Caused by Disruption of the FBN1 Gene due to A Reciprocal Chromosome Translocation 2021 ·Genes ·(unknown), Katalin Komlósi, (unknown), Jürgen Neesen, Paul Dremsek, Thomas Schwarz, Andreas Tzschach, (unknown), Ekkehart Lausch, Judith Fischer, Birgitta Gläser	16
4	New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation 2020 ·International Journal of Molecular Sciences ·Dominique Endres, Niels Decher, (unknown), (unknown), Katharina Domschke, Katalin Komlósi, Andreas Tzschach, Birgitta Gläser, Miriam A. Schiele, Kimon Runge, Patrick Süß, Florian Schuchardt, Kathrin Nickel, Birgit Stallmeyer, Susanne Rinné, Eric Schulze‐Bahr, Ludger Tebartz van Elst	15
5	Modeling MyD88 Deficiency In Vitro Provides New Insights in Its Function 2020 ·Frontiers in Immunology ·(unknown), (unknown), Roland Elling, Jamal Alzubi, (unknown), Julia Kolter, (unknown), (unknown), Birgitta Gläser, Sandra Ammann, Zoltán Ivics, Judith Fischer, Carsten Speckmann, Klaus Schwarz, Nico Lachmann, Stephan Ehl, Thomas Moritz, Philipp Henneke, Toni Cathomen	8
6	Schizophrenia and Hereditary Polyneuropathy: PMP22 Deletion as a Common Pathophysiological Link? 2019 ·Frontiers in Psychiatry ·Dominique Endres, Simon Maier, Christiane Ziegler, Kathrin Nickel, (unknown), Benjamin Berger, Johann Lambeck, (unknown), Birgitta Gläser, Friedrich Stock, Michael Dacko, Thomas Lange, Irina Mader, Katharina Domschke, Ludger Tebartz van Elst	3
7	Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report 2018 ·BMC Psychiatry ·Kathrin Nickel, Ludger Tebartz van Elst, Katharina Domschke, Birgitta Gläser, Friedrich Stock, Dominique Endres, Simon Maier, Andreas Riedel	10
8	Molecular cytogenetic analysis of a de novo balanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations 2003 ·American Journal of Medical Genetics Part A ·Birgitta Gläser, Katayoon Shirneshan, Karin Bink, Jutta Wirth, Hildegard Kehrer‐Sawatzki, (unknown), Barbara Zoll, Stefan K. Bohlander	10
9	Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies 2002 ·American Journal of Medical Genetics Part A ·Birgitta Gläser, Eva Rossier, Gotthold Barbi, Loredana Delle Chiaie, C. E. Blank, Walther Vogel, Hildegard Kehrer‐Sawatzki	12
10	The murine BTB/POZ zinc finger gene Znf131: predominant expression in the developing central nervous system, in adult brain, testis, and thymus 2002 ·Biochemical and Biophysical Research Communications ·Ralf Ulrich Trappe, (unknown), (unknown), Birgitta Gläser, (unknown), Wolfgang Engel, Peter Burfeind	18
11	Identification and characterization of murine <i>Brunol4</i>, a new member of the elav/bruno family 2002 ·Cytogenetic and Genome Research ·Moritz Meins, (unknown), Christian Wilhelm, (unknown), Shobha Yadav, Birgitta Gläser, Michal Grzmil, Patricia Burfeind, Franco Laccone	16
12	Identification and characterization of a novel murine multigene family containing a PHD-finger-like motif 2002 ·Biochemical and Biophysical Research Communications ·Ralf Ulrich Trappe, (unknown), Birgitta Gläser, Christine Vogel, (unknown), Peter Burfeind, Wolfgang Engel	33
13	Tep22, a novel testicular expressed gene, is involved in the biogenesis of the acrosome and the midpiece of the sperm tail 2002 ·Biochemical and Biophysical Research Communications ·Jürgen Neesen, Tobias M.P. Hartwich, Gunnar Brandhorst, Gerhard Aumüller, Birgitta Gläser, Peter Burfeind, Irene Mendoza-Lujambio	10
14	Isolation and Characterization of the Human Forkhead Gene FOXQ1 2001 ·DNA and Cell Biology ·(unknown), Bastian Pasche, Susanne Frank, Birgitta Gläser, Jürgen Kunz, (unknown), Barbara Zoll	61
15	Transposition of SRY into the ancestral pseudoautosomal region creates a new pseudoautosomal boundary in a progenitor of simian primates [In Process Citation] 1999 ·Human Molecular Genetics ·Birgitta Gläser	23
16	Simian Y Chromosomes: species-specific rearrangements of DAZ, RBM, and TSPY versus contiguity of PAR and SRY 1998 ·Mammalian Genome ·Birgitta Gläser, Frank Grützner, (unknown), Roscoe Stanyon, Norbert Arnold, Kay Taylor, (unknown), (unknown), Roland Toder, W. Schempp	50
17	Genes Located In and Near the Human Pseudoautosomal Region are Located in the X-Y Pairing Region in Dog and Sheep 1997 ·Chromosome Research ·Roland Toder, Birgitta Gläser, K. Schiebel, (unknown), Gudrun Rappold, Jennifer A. Marshall Graves, W. Schempp	35
18	FISH localization of the human Y-homolog of protein kinase PRKX (PRKY) to Yp11.2 and two pseudogenes to 15q26 and Xq12→q13 1997 ·Cytogenetic and Genome Research ·K. Schiebel, Annelyse Mertz, M. Winkelmann, Birgitta Gläser, W. Schempp, Gudrun Rappold	19
19	High-resolution fluorescencein situ hybridization ofRBM- andTSPY-related cosmids on released Y chromatin in humans and pygmy chimpanzees 1996 ·Chromosome Research ·Christian Conrad, Thomas Hierl, Birgitta Gläser, Kay Taylor, (unknown), Ann C. Chandley, W. Schempp	17
20	A naturally occurring short variant of the FTZ-F1-related nuclear orphan receptor xFF1rA and interactions between domains of xFF1rA. 1995 ·Molecular Endocrinology ·Heidrun Ellinger‐Ziegelbauer, Birgitta Gläser, C Dreyer	23

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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