Birgit Weiß

2.2k citations

23 papers · 1.6k indexed · 1 hit paper · h-index 16

Impact in

Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Developmental Biology top 10%

Papers in ⓘ

Genetics 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
Developmental Neuroscience 1

Co-authors: Gudrun Rappold (21 shared papers)Stefan Kirsch (4 shared papers)Beate Niesler (2 shared papers)Maki Fukami (3 shared papers)Tsutomu Ogata (3 shared papers)Gerhard Binder (2 shared papers)M. Winkelmann (1 shared paper)Andreas Rump (1 shared paper)
Journals: Nature Genetics (3 papers)Frontiers in Endocrinology (2 papers)Genomics (2 papers)Human Molecular Genetics (1 paper)FEBS Letters (1 paper)
Partner nations: Germany United States Netherlands

In The Last Decade

Birgit Weiß

23 papers receiving 1.6k citations

Hit Papers

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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome 1997 · 701 citations

Peers

Countries citing papers authored by Birgit Weiß

Since Specialization

Citations

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

Fields of papers citing papers by Birgit Weiß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Birgit Weiß, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Birgit Weiß Line = papers co-authored together Birgit Weiß links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome Nature Genetics ·Ercole Rao, Birgit Weiß, Maki Fukami, Andreas Rump, Beate Niesler, Annelyse Mertz, Koji Muroya, Gerhard Binder, Stefan Kirsch, M. Winkelmann, Gabriele Nordsiek, U. Heinrich, M.H. Breuning, Michael B. Ranke, André Rosenthal, Tsutomu Ogata, Gudrun Rappold Hit paper breakdown →	1997	701
2	Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation Nature Genetics ·Simone Berkel, Christian R. Marshall, Birgit Weiß, Jennifer Howe, Ralph Roeth, Ute Moog, Volker Endris, Wendy Roberts, Péter Szatmári, Dalila Pinto, Michael Bonin, Angelika Rieß, Hartmut Engels, Rolf Sprengel, Stephen W. Scherer, Gudrun Rappold	2010	410
3	A human pseudoautosomal gene, ADP/ATP translocase, escapes X–inactivation whereas a homologue on Xq is subject to X–inactivation Nature Genetics ·K. Schiebel, Birgit Weiß, Doris Wöhrle, Gudrun Rappold	1993	68
4	Expression of Apolipoprotein A‐I in Porcine Brain Endothelium In Vitro Journal of Neurochemistry ·Babette Möckel, Holger Zinke, Regina Flach, Birgit Weiß, Hartmut Weiler‐Güttler, Hans Günter Gassen	1994	63
5	Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients. Pharmacogenetics ·Beate Niesler, Birgit Weiß, Christine Fischer, Markus M. Nöthen, Peter Propping, Brigitta Bondy, Marcella Rietschel, Wolfgang Maier, Margot Albus, Ernst Franzek, Gudrun Rappold	2001	52
6	BNP is a transcriptional target of the short stature homeobox gene SHOX Human Molecular Genetics ·Antonio Marchini, Beate Häcker, Tiina Marttila, V. Hesse, Joyce Emons, Birgit Weiß, Marcel Karperien, Gudrun Rappold	2007	46
7	Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation Basic Research in Cardiology ·Sandra Hoffmann, Sebastian Clauß, Ina M. Berger, Birgit Weiß, Antonino Montalbano, Ralph Röth, Madeline Bucher, Ina Klier, Reza Wakili, Hervé Seitz, Eric Schulze‐Bahr, Hugo A. Katus, Friederike Flachsbart, Almut Nebel, S. Guenther, Erik Bagaev, Wolfgang Rottbauer, Stefan Kääb, Steffen Just, Gudrun Rappold	2016	36
8	Biodiversity, the ultimate agri-environmental indicator? Agriculture Ecosystems & Environment ·Wolfgang Büchs, Alexandra Harenberg, Joachim Zimmermann, Birgit Weiß	2003	35
9	Organisation of the murine 5‐HT₃ receptor gene and assignment tohuman chromosome 11 FEBS Letters ·Peter Uetz, Fawzy Abdelatty, Alfredo Villarroel, Gudrun Rappold, Birgit Weiß, Michael Koenen	1994	31
10	Investigation of SHANK3 in schizophrenia American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ana de Sena Cortabitarte, Franziska Degenhardt, Jana Strohmaier, Maren Lang, Birgit Weiß, Ralph Roeth, Ina Giegling, Stefanie Heilmann‐Heimbach, Andrea Hofmann, Dan Rujescu, Christine Fischer, Marcella Rietschel, Markus M. Nöthen, Gudrun Rappold, Simone Berkel	2017	31
11	Interchromosomal segmental duplications of the pericentromeric region on the human Y chromosome Genome Research ·Stefan Kirsch, Birgit Weiß, Tracie L. Miner, R Waterston, Royden A. Clark, Evan E. Eichler, Claudia Münch, W. Schempp, Gudrun Rappold	2005	28
12	Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency EMBO Molecular Medicine ·Antonino Montalbano, Lonny Juergensen, Ralph Roeth, Birgit Weiß, Maki Fukami, Susanne Fricke‐Otto, Gerhard Binder, Tsutomu Ogata, Eva L. Decker, Gudrun Nuernberg, David Hassel, Gudrun Rappold	2016	18
13	Assignment of a Human Homolog of the Mouse Htr3 Receptor Gene to Chromosome 11q23.1-q23.2 Genomics ·Birgit Weiß, Annelyse Mertz, Evelin Schröck, Michael Koenen, Gudrun Rappold	1995	18
14	Functional Characterization of Rare Variants in the SHOX2 Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation Frontiers in Genetics ·Sandra Hoffmann, Christoph Paone, Simon Sumer, Sabrina Diebold, Birgit Weiß, Ralph Roeth, Sebastian Clauß, Ina Klier, Stefan Kääb, Andreas Schulz, Philipp S. Wild, Adil Ghrib, Tanja Zeller, Renate B. Schnabel, Steffen Just, Gudrun Rappold	2019	17
15	Molecular and evolutionary analysis of the growth-controlling region on the human Y chromosome Human Genetics ·Stefan Kirsch, Birgit Weiß, Klaus Ulrich Zumbach, Gudrun Rappold	2004	16
16	Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency Genetics in Medicine ·Franziska Simm, Anne Griesbeck, Daniela Choukair, Birgit Weiß, Nagarajan Paramasivam, Jürgen Klammt, Matthias Schlesner, Stefan Wiemann, Cristina Martínez, Georg F. Hoffmann, Roland Pfäffle, Markus Bettendorf, Gudrun Rappold	2017	16
17	Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature European Journal of Human Genetics ·Antonino Montalbano, Lonny Juergensen, Maki Fukami, Christian T. Thiel, Nadine H Hauer, Ralph Roeth, Birgit Weiß, Yasuhiro Naiki, Tsutomu Ogata, David Hassel, Gudrun Rappold	2018	11
18	The definition of the Y chromosome growth-control gene (GCY) critical region: relevance of terminal and interstitial deletions. PubMed ·Stefan Kirsch, Birgit Weiß, Karin Schön, Gudrun Rappold	2002	11
19	Identification of <b><i>Transient Receptor Potential Channel 4-Associated Protein</i></b> as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism Hormone Research in Paediatrics ·Daniela Choukair, Birgit Eberle, Philipp Vick, Pia Hermanns, Birgit Weiß, Nagarajan Paramasivam, Matthias Schlesner, Katharina Lornsen, Ralph Roeth, Carina Klutmann, Jennifer Kreis, Georg F. Hoffmann, Joachim Pohlenz, Gudrun Rappold, Markus Bettendorf	2020	10
20	Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes Frontiers in Endocrinology ·Birgit Weiß, Birgit Eberle, Ralph Roeth, Christiaan de Bruin, Julian C. Lui, Nagarajan Paramasivam, Katrin Hinderhofer, Hermine A. van Duyvenvoorde, Jeffrey Baron, Jan M. Wit, Gudrun Rappold	2021	5

About Birgit Weiß

Birgit Weiß is a scholar working on Genetics, Developmental Neuroscience, Molecular Biology, Gender Studies and Endocrinology, Diabetes and Metabolism, having authored 23 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genomics and Chromatin Dynamics (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Thyroid Disorders and Treatments (2 papers), Autism Spectrum Disorder Research (2 papers), Retinoids in leukemia and cellular processes (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (1.1k citations), Developmental Biology (32 citations), Gender Studies (138 citations), Molecular Biology (986 citations) and Cognitive Neuroscience (247 citations). Birgit Weiß has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Gudrun Rappold, Stefan Kirsch, Beate Niesler, Maki Fukami, Tsutomu Ogata, Gerhard Binder, M. Winkelmann, Andreas Rump, Ercole Rao and Michael B. Ranke. Their work appears in journals such as Nature Genetics, Frontiers in Endocrinology, Genomics, Human Molecular Genetics and FEBS Letters.

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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