Beate Albrecht

8.4k citations

45 papers · 1.7k indexed · h-index 23

Genetics top 2%
Molecular Biology top 10%
Pediatrics, Perinatology and Child Health top 5%
Surgery
Plant Science

Co-authors: Bernhard Horsthemke Gabriele Gillessen‐Kaesbach Peter Meinecke Dagmar Wieczorek Hermann‐Josef Lüdecke Denise Horn Frank Majewski Raoul C. M. Hennekam
Topics: Prenatal Screening and Diagnostics (10 papers)Genetic Syndromes and Imprinting (9 papers)Genomic variations and chromosomal abnormalities (9 papers)
Cited by: Genetics Developmental Biology Pediatrics, Perinatology and Child Health
Journals: Nature GeneticsSHILAP Revista de lepidopterologíaThe American Journal of Human Genetics
Partner nations: Germany United States United Kingdom

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-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

#	Work	Indexed citations
1	New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome 2017 ·European Journal of Human Genetics ·Jasmin Beygo,(unknown),Gabriele Gillessen‐Kaesbach,Beate Albrecht,(unknown),Thomas Eggermann,Alexandra Gellhaus,Deniz Kanber,(unknown),Hermann‐Josef Lüdecke,Sabine Purmann,Eva Rossier,Johannes van de Nes,Ilse M. van der Werf,(unknown),Dagmar Wieczorek,Bernhard Horsthemke,Karin Buiting	31
2	Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly 2016 ·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,(unknown),Ahmet Okay Çağlayan,Jiri Vajsar,Kaya Bilgüvar,Gönül Oğur,Rami Abou Jamra,Murat Günel,Joseph G. Gleeson	33
3	De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations 2016 ·American Journal of Medical Genetics Part A ·(unknown),Hartmut Engels,Kirsten Cremer,Jessica Becker,Eva Wohlleber,Beate Albrecht,(unknown),Hermann‐Josef Lüdecke,Mohnish Suri,(unknown),Alessandra Renieri,Guido Kukuk,Thomas Wieland,Joris Andrieux,Tim M. Strom,Dagmar Wieczorek,Anne Dieux‐Coëslier,Alexander M. Zink	13
4	Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities? 2015 ·American Journal of Medical Genetics Part A ·Karl Hackmann,Andreas Rump,Stefan A. Haas,Johannes R. Lemke,Jean‐Pierre Fryns,Andreas Tzschach,Dagmar Wieczorek,Beate Albrecht,Alma Kuechler,Tim Ripperger,(unknown),Konrad Oexle,Sigrid Tinschert,Evelin Schröck,Vera M. Kalscheuer,Nataliya Di Donato	8
5	Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome 2015 ·Journal of Medical Genetics ·(unknown),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,(unknown),Susanne J. Kühl,Usha Kini,Alisdair McNeill	53
6	A patient with a de-novo deletion 3p25.3 and features overlapping with Rubinstein–Taybi syndrome 2014 ·Clinical Dysmorphology ·Johanna Christina Czeschik,Beate Albrecht,Hülya Kayserili,Alma Kuechler,Nicholas Wagner,Dagmar Wieczorek,Hermann‐Josef Lüdecke	2
7	Monozygotic twins discordant for trisomy 18 2011 ·Ultrasound in Obstetrics and Gynecology ·A. Reuss,H. Gerlach,(unknown),(unknown),Ulrich Kühn,Anja Stein,(unknown),Beate Albrecht,(unknown),(unknown),B. Eiben	12
8	Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies 2011 ·Molecular Syndromology ·Fanny Kortüm,(unknown),Sigrid Fuchs,Beate Albrecht,Gabriele Gillessen‐Kaesbach,Ulrike Mütze,E Seemanová,Sigrid Tinschert,Dagmar Wieczorek,Georg Rosenberger,Kerstin Kutsche	7
9	Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene 2011 ·Clinical Genetics ·Rebecca Nagy,(unknown),Beate Albrecht,Dagmar Wieczorek,(unknown),Eric Haan,Peter Meinecke,Albert de la Chapelle,(unknown)	26
10	An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistance 2010 ·European Journal of Human Genetics ·A. Kuechler,Berthold P. Hauffa,Angela Köninger,Gunnar Kleinau,Beate Albrecht,Bernhard Horsthemke,Jörg Gromoll	56
11	Präklinische Kindernotfälle. Notärztliche Wahrnehmung und Einschätzung. 2009 ·Der Anaesthesist ·Christoph Eich,Markus Roeßler,A. Timmermann,Jan Heuer,(unknown),Beate Albrecht,Sebastian G. Russo	3
12	Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein–Taybi syndrome 2009 ·American Journal of Medical Genetics Part A ·Oliver Bartsch,(unknown),Beate Albrecht,Dagmar Wieczorek,(unknown),Ulrich Zechner,Thomas Haaf	44
13	Spondylocheiro Dysplastic Form of the Ehlers-Danlos Syndrome—An Autosomal-Recessive Entity Caused by Mutations in the Zinc Transporter Gene SLC39A13 2008 ·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	149
14	IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia 2007 ·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	49
15	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) 2005 ·American Journal of Medical Genetics Part A ·Susanne Zahn,(unknown),Kristin Bosse,Vera M. Kalscheuer,Peter Propping,Gesa Schwanitz,Beate Albrecht,Hartmut Engels	15
16	Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3 2005 ·Biological Chemistry ·Dieter E. Jenne,(unknown),Matthias Vorgerd,J. M. Schröder,Joachim Weis,(unknown),Beate Albrecht,Peter Nürnberg,Holger Thiele,Clemens R. Müller,Gerhard Meng,Christian Witt,Siegfried Labeit	10
17	Mosaic trisomy 15 in a short girl with hemihypotrophy and mental retardation 2004 ·Clinical Dysmorphology ·(unknown),Annette Richter-Unruh,Beate Albrecht,Gabriele Gillessen‐Kaesbach,Berthold P. Hauffa	5
18	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 2004 ·European Journal of Pediatrics ·Annette Richter-Unruh,(unknown),Stefan Kaspers,Beate Albrecht,Gabriele Gillessen‐Kaesbach,Berthold P. Hauffa	35
19	Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes 2003 ·European Journal of Human Genetics ·Seval Türkmen,Gabriele Gillessen‐Kaesbach,Peter Meinecke,Beate Albrecht,Luitgard M. Neumann,V. Hesse,Şükrü Palanduz,(unknown),Frank Majewski,Sigrun Fuchs,(unknown),(unknown),(unknown),Friedmar R. Kreuz,(unknown),Burkhard Rodeck,Jürgen Kunze,Sigrid Tinschert,Stefan Mundlos,Denise Horn	97
20	Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I 2000 ·Nature Genetics ·Parastoo Momeni,Gernot Glöckner,Olaf Schmidt,(unknown),Beate Albrecht,Gabriele Gillessen-Kaesbach,Raoul C. M. Hennekam,Peter Meinecke,Bernhard Zabel,André Rosenthal,Bernhard Horsthemke,Hermann‐Josef Lüdecke	241

About Beate Albrecht

Beate Albrecht is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 45 papers that have together received 1.7k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (10 papers), Genetic Syndromes and Imprinting (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). The work is most often cited by research in Genetics (1.0k citations), Developmental Biology (62 citations) and Pediatrics, Perinatology and Child Health (264 citations). Beate Albrecht has collaborated with scholars based in Germany, United States and United Kingdom. Frequent 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. Their work appears in journals such as Nature Genetics, SHILAP Revista de lepidopterología and The American Journal of Human 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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