Beate Albrecht

8.4k total citations
45 papers, 1.7k citations indexed

About

Beate Albrecht is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Beate Albrecht has authored 45 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 22 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Beate Albrecht's work include Prenatal Screening and Diagnostics (10 papers), Genetic Syndromes and Imprinting (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Beate Albrecht is often cited by papers focused on Prenatal Screening and Diagnostics (10 papers), Genetic Syndromes and Imprinting (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Beate Albrecht collaborates with scholars based in Germany, United States and United Kingdom. Beate Albrecht's co-authors include Bernhard Horsthemke, Gabriele Gillessen‐Kaesbach, Peter Meinecke, Dagmar Wieczorek, Hermann‐Josef Lüdecke, Denise Horn, Frank Majewski, Raoul C. M. Hennekam, Andreas Janecke and Parastoo Momeni and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Beate Albrecht

45 papers receiving 1.6k citations

Peers

Beate Albrecht

GENET

PPCH

SURGE

Alan Shanske United States

Małgorzata Krajewska‐Walasek Poland

Sarina G. Kant Netherlands

Maria Hoeltzenbein Germany

Stefania Gimelli Switzerland

Kwame Anyane‐Yeboa United States

Gioacchino Scarano Italy

Zvi Borochowitz Israel

G. Shashidhar Pai United States

Susan Holder United Kingdom

Alan Shanske United States

Beate Albrecht

931 ×0.9

GENET

976 ×1.1

310 ×1.2

PPCH

240 ×1.1

SURGE

193 ×1.3

Citations per year, relative to Beate Albrecht Beate Albrecht (= 1×) peers Alan Shanske

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-authorship network of co-authors of Beate Albrecht

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

Beygo, Jasmin, Gabriele Gillessen‐Kaesbach, Beate Albrecht, et al.. (2017). 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. 25(8). 935–945. 31 indexed citations

Jerber, Julie, Maha S. Zaki, Jumana Y. Al‐Aama, et al.. (2016). Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly. The American Journal of Human Genetics. 99(5). 1181–1189. 33 indexed citations

Engels, Hartmut, Kirsten Cremer, Jessica Becker, et al.. (2016). De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations. American Journal of Medical Genetics Part A. 173(2). 435–443. 13 indexed citations

Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations

Pagnamenta, Alistair T., Moira Blyth, Sahar Mansour, et al.. (2015). Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. Journal of Medical Genetics. 53(3). 152–162. 53 indexed citations

Czeschik, Johanna Christina, Beate Albrecht, Hülya Kayserili, et al.. (2014). A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein–Taybi syndrome. Clinical Dysmorphology. 23(2). 67–70. 2 indexed citations

Reuss, A., H. Gerlach, Ulrich Kühn, et al.. (2011). Monozygotic twins discordant for trisomy 18. Ultrasound in Obstetrics and Gynecology. 38(6). 727–728. 12 indexed citations

Kortüm, Fanny, Sigrid Fuchs, Beate Albrecht, et al.. (2011). Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies. Molecular Syndromology. 2(1). 27–34. 7 indexed citations

Nagy, Rebecca, Beate Albrecht, Dagmar Wieczorek, et al.. (2011). Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene. Clinical Genetics. 82(2). 140–146. 26 indexed citations

10.

Kuechler, A., Berthold P. Hauffa, Angela Köninger, et al.. (2010). An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistance. European Journal of Human Genetics. 18(6). 656–661. 56 indexed citations

11.

Eich, Christoph, Markus Roeßler, A. Timmermann, et al.. (2009). Präklinische Kindernotfälle. Notärztliche Wahrnehmung und Einschätzung.. Der Anaesthesist. 58(9). 876–883. 3 indexed citations

12.

Bartsch, Oliver, et al.. (2009). Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein–Taybi syndrome. American Journal of Medical Genetics Part A. 152A(1). 181–184. 44 indexed citations

13.

Giunta, Cecilia, Nursel Elçioğlu, Beate Albrecht, et al.. (2008). 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. 82(6). 1290–1305. 149 indexed citations

14.

Zeschnigk, Michael, Beate Albrecht, Karin Buiting, et al.. (2007). IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia. European Journal of Human Genetics. 16(3). 328–334. 49 indexed citations

15.

Zahn, Susanne, Kristin Bosse, Vera M. Kalscheuer, et al.. (2005). Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1). American Journal of Medical Genetics Part A. 139A(1). 19–24. 15 indexed citations

16.

Jenne, Dieter E., Matthias Vorgerd, J. M. Schröder, et al.. (2005). Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3. Biological Chemistry. 386(1). 61–7. 10 indexed citations

17.

Richter-Unruh, Annette, et al.. (2004). Mosaic trisomy 15 in a short girl with hemihypotrophy and mental retardation. Clinical Dysmorphology. 13(3). 183–186. 5 indexed citations

18.

Richter-Unruh, Annette, et al.. (2004). 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. 163(4-5). 251–256. 35 indexed citations

19.

Türkmen, Seval, Gabriele Gillessen‐Kaesbach, Peter Meinecke, et al.. (2003). Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. European Journal of Human Genetics. 11(11). 858–865. 97 indexed citations

20.

Momeni, Parastoo, Gernot Glöckner, Olaf Schmidt, et al.. (2000). Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I. Nature Genetics. 24(1). 71–74. 241 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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