Beate Albrecht

8.5k citations

45 papers · 1.7k · h-index 23

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
- Genetics and Neurodevelopmental Disorders
Developmental Biology top 5%

Papers in

Genetics 27
- Genomic variations and chromosomal abnormalities 9
- Genetic Syndromes and Imprinting 9
- Connective tissue disorders research 5
Molecular Biology 21
- Epigenetics and DNA Methylation 6
- Genomics and Chromatin Dynamics 5

Co-authors: Bernhard Horsthemke (5 shared papers)Gabriele Gillessen‐Kaesbach (10 shared papers)Peter Meinecke (5 shared papers)Dagmar Wieczorek (12 shared papers)Hermann‐Josef Lüdecke (5 shared papers)Denise Horn (4 shared papers)Frank Majewski (3 shared papers)Andreas Janecke (2 shared papers)
Journals: European Journal of Human Genetics (8 papers)The American Journal of Human Genetics (3 papers)Human Mutation (3 papers)Journal of Medical Genetics (2 papers)European Journal of Medical Genetics (1 paper)
Partner nations: Germany United States Belgium

In The Last Decade

Beate Albrecht

45 papers receiving 1.6k citations

Peers

Countries citing papers authored by Beate Albrecht

Since Specialization

Citations

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

Fields of papers citing papers by Beate Albrecht

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Beate Albrecht, 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 Beate Albrecht Line = papers co-authored together Beate Albrecht links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I Nature Genetics ·Parastoo Momeni, Gernot Glöckner, Olaf Schmidt, D. von Holtum, Beate Albrecht, Gabriele Gillessen-Kaesbach, Raoul C. M. Hennekam, Peter Meinecke, Bernhard Zabel, André Rosenthal, Bernhard Horsthemke, Hermann‐Josef Lüdecke	2000	244
2	Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification European Journal of Medical Genetics ·Christiane Tasse, Stefan Böhringer, Sven Fischer, Hermann‐Josef Lüdecke, Beate Albrecht, Denise Horn, Andreas Janecke, Rainer Kling, Rainer König, Birgit Lorenz, Frank Majewski, Elisabeth Maeyens, Peter Meinecke, Beate Mitulla, Christopher Mohr, Monika Preischl, H. E. Umstadt, Jürgen Kohlhase, Gabriele Gillessen‐Kaesbach, Dagmar Wieczorek	2005	158
3	Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13 The American Journal of Human Genetics ·Cecilia Giunta, Nursel Elçioğlu, Beate Albrecht, Georg Eich, Céline Chambaz, Andreas Janecke, Heather N. Yeowell, MaryAnn Weis, David R. Eyre, Marius Kraenzlin, Beat Steinmann	2008	150
4	Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes European Journal of Human Genetics ·Seval Türkmen, Gabriele Gillessen‐Kaesbach, Peter Meinecke, Beate Albrecht, Luitgard M. Neumann, V. Hesse, Şükrü Palanduz, S. Balg, Frank Majewski, Sigrun Fuchs, Petra Zschieschang, M. Greiwe, K. Mennicke, Friedmar R. Kreuz, Harald J Dehmel, Burkhard Rodeck, Jürgen Kunze, Sigrid Tinschert, Stefan Mundlos, Denise Horn	2003	97
5	Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements European Journal of Human Genetics ·Heike Starke, Jörg Seidel, Wolfram Henn, Sylvia Reichardt, Marianne Volleth, Markus Stümm, Christine Behrend, K. R. Sandig, Christine Kelbova, Gabriele Senger, Beate Albrecht, I. Hansmann, Anita Heller, Uwe Claussen, Thomas Liehr	2002	91
6	“Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene American Journal of Medical Genetics ·Christiane Zweier, Beate Albrecht, Beate Mitulla, R. Behrens, Maike Beese, Gabriele Gillessen‐Kaesbach, Hans‐Dieter Rott, Anita Rauch	2002	89
7	New insights into the pathogenesis of autosomal‐dominant cutis laxa with report of fiveELNmutations Human Mutation ·Bert Callewaert, Marjolijn Renard, Vishwanathan Hucthagowder, Beate Albrecht, Ingrid Haußer, Edward Blair, Cristina Dias, Alice Albino, Hiroshi Wachi, Fumiaki Sato, Robert P. Mecham, Bart Loeys, Paul Coucke, Anne De Paepe, Zsolt Urbán	2011	83
8	Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion European Journal of Human Genetics ·Dagmar Wieczorek, Mario Krause, Frank Majewski, Beate Albrecht, Denise Horn, Olaf Rieß, Gabriele Gillessen‐Kaesbach	2000	75
9	An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistance European Journal of Human Genetics ·(unknown), Berthold P. Hauffa, Angela Köninger, Gunnar Kleinau, Beate Albrecht, Bernhard Horsthemke, Jörg Gromoll	2010	58
10	Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprintedDLK1/GTL2gene cluster Human Mutation ·Karin Buiting, Deniz Kanber, José I. Martín‐Subero, Wolfgang Lieb, Paulien A. Terhal, Beate Albrecht, Sabine Purmann, Stephanie Groß, Christina Lich, Reiner Siebert, Bernhard Horsthemke, Gabriele Gillessen‐Kaesbach	2008	57
11	Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome Journal of Medical Genetics ·Annmarie Hempel, Alistair T. Pagnamenta, Moira Blyth, Sahar Mansour, Vivienne McConnell, Ikuyo Kou, Shiro Ikegawa, Yoshinori Tsurusaki, Naomichi Matsumoto, Adriana Lo‐Castro, Ghislaine Plessis, Beate Albrecht, Agatino Battaglia, Jenny C. Taylor, Malcolm F. Howard, David A. Keays, Aman Singh Sohal, Susanne J. Kühl, Usha Kini, Alisdair McNeill	2015	53
12	IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia European Journal of Human Genetics ·Michael Zeschnigk, Beate Albrecht, Karin Buiting, Deniz Kanber, Thomas Eggermann, Gerhard Binder, Jörg Gromoll, Eva‐Christina Prott, Saskia Seland, Bernhard Horsthemke	2007	51
13	Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein–Taybi syndrome American Journal of Medical Genetics Part A ·Oliver Bartsch, Janette Labonté, Beate Albrecht, Dagmar Wieczorek, Stanislav Lechno, Ulrich Zechner, Thomas Haaf	2009	44
14	Detection of heterozygousSALL1 deletions by quantitative real time PCR proves the contribution of aSALL1 dosage effect in the pathogenesis of Townes-Brocks syndrome Human Mutation ·Wiktor Borozdin, Katharina Steinmann, Beate Albrecht, Armand Bottani, Koenraad Devriendt, M. Leipoldt, Jürgen Kohlhase	2006	38
15	Short stature in children with an apparently normal male phenotype can be caused by 45,X/46,XY mosaicism and is susceptible to growth hormone treatment European Journal of Pediatrics ·Annette Richter-Unruh, Sabine Knauer-Fischer, Stefan Kaspers, Beate Albrecht, Gabriele Gillessen‐Kaesbach, Berthold P. Hauffa	2004	35
16	Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly The American Journal of Human Genetics ·Julie Jerber, Maha S. Zaki, Jumana Y. Al‐Aama, Rasim Özgür Rosti, Tawfeg Ben‐Omran, Esra Dikoglu, Jennifer L. Silhavy, Caner Çağlar, Damir Musaev, Beate Albrecht, Kevin P. Campbell, Tobias Willer, Mariam Almuriekhi, Ahmet Okay Çağlayan, Jiri Vajsar, Kaya Bilgüvar, Gönül Oğur, Rami Abou Jamra, Murat Günel, Joseph G. Gleeson	2016	34
17	New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome European Journal of Human Genetics ·Jasmin Beygo, Alma Küchler, Gabriele Gillessen‐Kaesbach, Beate Albrecht, Jonas Eckle, Thomas Eggermann, Alexandra Gellhaus, Deniz Kanber, Ulrike Kordaß, Hermann‐Josef Lüdecke, Sabine Purmann, Eva Rossier, Johannes van de Nes, Ilse M. van der Werf, Maren Wenzel, Dagmar Wieczorek, Bernhard Horsthemke, Karin Buiting	2017	31
18	Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability European Journal of Human Genetics ·Frédéric Tran Mau‐Them, Marjolaine Willems, Beate Albrecht, Elodie Sanchez, Jacques Puechberty, Sabine Endele, Anouck Schneider, Nathalie Pallarès, Chantal Missirian, François Rivier, Manon Girard, Muriel Holder, Sylvie Manouvrier, Isabelle Touitou, Geneviève Lefort, Pierre Sarda, Anne Moncla, Séverine Drunat, Dagmar Wieczorek, David Geneviève	2013	30
19	Childhood overgrowth in patients with common NF1 microdeletions European Journal of Human Genetics ·Miriam Spiegel, Konrad Oexle, Denise Horn, Elke Windt, Annegret Buske, Beate Albrecht, Eva‐Christina Prott, E Seemanová, J. Seidel, Thorsten Rosenbaum, Dieter E. Jenne, Hildegard Kehrer‐Sawatzki, Sigrid Tinschert	2005	30
20	Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene Clinical Genetics ·Rebecca Nagy, H Wang, Beate Albrecht, Dagmar Wieczorek, G. Gillessen Kaesbach, Eric Haan, Peter Meinecke, Albert de la Chapelle, J C Westman	2011	26

About Beate Albrecht

Beate Albrecht is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Plant Science, having authored 45 papers that have together received 1.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (6 papers), Connective tissue disorders research (5 papers), Chromosomal and Genetic Variations (5 papers), Genomics and Chromatin Dynamics (5 papers) and Congenital limb and hand anomalies (3 papers). The work is most often cited by research in Genetics (977 citations), Developmental Biology (58 citations), Pediatrics, Perinatology and Child Health (216 citations), Molecular Biology (761 citations) and Genetics (97 citations). Beate Albrecht has collaborated with scholars based in Germany, United States and Belgium. Frequent co-authors include Bernhard Horsthemke, Gabriele Gillessen‐Kaesbach, Peter Meinecke, Dagmar Wieczorek, Hermann‐Josef Lüdecke, Denise Horn, Frank Majewski, Andreas Janecke, Raoul C. M. Hennekam and Beate Mitulla. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Mutation, Journal of Medical Genetics and European Journal of Medical Genetics.

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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