Rebecca Buchert

1.8k total citations
26 papers, 645 citations indexed

About

Rebecca Buchert is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Rebecca Buchert has authored 26 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Oncology. Recurrent topics in Rebecca Buchert's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers) and Cellular transport and secretion (5 papers). Rebecca Buchert is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers) and Cellular transport and secretion (5 papers). Rebecca Buchert collaborates with scholars based in Germany, Pakistan and Japan. Rebecca Buchert's co-authors include Rami Abou Jamra, André Reis, Arif B. Ekici, Hasan Tawamie, Heinrich Sticht, Markus M. Nöthen, Laurence Colleaux, Elisabeth Graf, Arnold Münnich and Tim M. Strom and has published in prestigious journals such as Nature Communications, Brain and The American Journal of Human Genetics.

In The Last Decade

Rebecca Buchert

25 papers receiving 639 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Rebecca Buchert Germany 13 333 154 139 136 104 26 645
Josef Ekstein United States 12 407 1.2× 193 1.3× 122 0.9× 170 1.3× 104 1.0× 27 851
Chihiro Ohba Japan 16 563 1.7× 341 2.2× 102 0.7× 252 1.9× 107 1.0× 26 922
Hanna Mierzewska Poland 15 444 1.3× 127 0.8× 55 0.4× 105 0.8× 82 0.8× 57 728
John J. McMahon United States 12 567 1.7× 155 1.0× 111 0.8× 224 1.6× 124 1.2× 14 874
Jean‐Baptiste Rivière Canada 18 591 1.8× 575 3.7× 141 1.0× 145 1.1× 79 0.8× 36 1.2k
Jay P. Ross Canada 15 226 0.7× 105 0.7× 79 0.6× 111 0.8× 97 0.9× 39 653
Alysen Clark Canada 5 482 1.4× 47 0.3× 49 0.4× 70 0.5× 96 0.9× 6 662
Youngshin Lim United States 12 334 1.0× 83 0.5× 120 0.9× 159 1.2× 69 0.7× 24 544
Vesna Ponjavic Sweden 22 875 2.6× 107 0.7× 110 0.8× 212 1.6× 51 0.5× 55 1.3k
Ercan Demir Türkiye 11 368 1.1× 65 0.4× 212 1.5× 237 1.7× 30 0.3× 24 732

Countries citing papers authored by Rebecca Buchert

Since Specialization
Citations

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

Fields of papers citing papers by Rebecca Buchert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca Buchert

This figure shows the co-authorship network connecting the top 25 collaborators of Rebecca Buchert. A scholar is included among the top collaborators of Rebecca Buchert 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 Rebecca Buchert. Rebecca Buchert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Laugwitz, Lucia, Rebecca Buchert, Mona Grimmel, et al.. (2024). Elevated cholesterol is a common phenotype for dominant and recessive ATAD3-associated disorders. Brain. 148(4). e24–e28. 1 indexed citations
2.
Faust, Ulrike, Gertrud Strobl‐Wildemann, Marc Sturm, et al.. (2023). Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome. Molecular Genetics & Genomic Medicine. 11(6). e2151–e2151. 3 indexed citations
3.
Bilal, Muhammad, et al.. (2023). Sequence Variants in the <i>WNT10B</i> Underlying Non-Syndromic Split-Hand/Foot Malformation. Molecular Syndromology. 14(6). 469–476.
4.
Bilal, Muhammad, Tobias B. Haack, Rebecca Buchert, et al.. (2023). Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly. European Journal of Human Genetics. 31(11). 1270–1274. 3 indexed citations
5.
Bilal, Muhammad, Tobias B. Haack, Rebecca Buchert, et al.. (2023). Sequence Variants in MEGF8 and GJA1 Underlying Syndactyly. Molecular Syndromology. 14(3). 201–207. 2 indexed citations
6.
Buchert, Rebecca, Thomas Hentrich, Nico Weber, et al.. (2022). Genome Sequencing and Transcriptome Profiling in Twins Discordant for Mayer-Rokitansky-Küster-Hauser Syndrome. Journal of Clinical Medicine. 11(19). 5598–5598. 9 indexed citations
7.
Rapp, Christina, Lucia Laugwitz, Mieke Boon, et al.. (2021). Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy. Clinical Genetics. 100(4). 453–461. 12 indexed citations
8.
Gburek‐Augustat, Janina, Jan‐Christoph Schoene‐Bake, Eva Bültmann, et al.. (2021). Pitfalls in Genetic Diagnostics: Why Phenotyping is Essential. Neuropediatrics. 52(4). 274–283. 1 indexed citations
9.
Bauer, Daniel, et al.. (2020). GlyT1 encephalopathy: Characterization of presumably disease causing GlyT1 mutations. Neurochemistry International. 139. 104813–104813. 5 indexed citations
10.
Laugwitz, Lucia, Rebecca Buchert, Samuel Groeschel, et al.. (2020). Pontocerebellar hypoplasia type 11: Does the genetic defect determine timing of cerebellar pathology?. European Journal of Medical Genetics. 63(7). 103938–103938. 5 indexed citations
11.
Rieß, Olaf, et al.. (2019). Two cases of variant late infantile ceroid lipofuscinosis in Jordan. World Journal of Clinical Cases. 7(2). 203–208. 3 indexed citations
12.
Mazaheri, Neda, Reza Azizi Malamiri, Nafi Dilaver, et al.. (2018). Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant. Neurological Sciences. 39(11). 1917–1925. 16 indexed citations
13.
Bréchet, Aline, Rebecca Buchert, Jochen Schwenk, et al.. (2017). AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability. Nature Communications. 8(1). 15910–15910. 56 indexed citations
14.
Tawamie, Hasan, Igor Martianov, Rebecca Buchert, et al.. (2017). Hypomorphic Pathogenic Variants in TAF13 Are Associated with Autosomal-Recessive Intellectual Disability and Microcephaly. The American Journal of Human Genetics. 100(3). 555–561. 18 indexed citations
15.
Han, Chanshuai, Reem A. Alkhater, Tawfiq Froukh, et al.. (2016). Epileptic Encephalopathy Caused by Mutations in the Guanine Nucleotide Exchange Factor DENND5A. The American Journal of Human Genetics. 99(6). 1359–1367. 27 indexed citations
16.
Buchert, Rebecca, Hasan Tawamie, Christopher Smith, et al.. (2014). A Peroxisomal Disorder of Severe Intellectual Disability, Epilepsy, and Cataracts Due to Fatty Acyl-CoA Reductase 1 Deficiency. The American Journal of Human Genetics. 95(5). 602–610. 95 indexed citations
17.
Riecken, Lars Björn, Hasan Tawamie, Rebecca Buchert, et al.. (2014). Inhibition of RAS Activation Due to a Homozygous Ezrin Variant in Patients with Profound Intellectual Disability. Human Mutation. 36(2). 270–278. 12 indexed citations
18.
Hansen, Lars Hestbjerg, Hasan Tawamie, Yoshiko Murakami, et al.. (2013). Hypomorphic Mutations in PGAP2, Encoding a GPI-Anchor-Remodeling Protein, Cause Autosomal-Recessive Intellectual Disability. The American Journal of Human Genetics. 92(4). 575–583. 73 indexed citations
19.
Buchert, Rebecca, Steffen Uebe, Hasan Tawamie, et al.. (2013). Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation. European Journal of Medical Genetics. 56(11). 599–602. 16 indexed citations
20.
Jamra, Rami Abou, Annick Raas‐Rothschild, Sebastian Eck, et al.. (2011). Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature. The American Journal of Human Genetics. 88(6). 788–795. 167 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Josef Ekstein Breakdown of academic impact, for papers by Chihiro Ohba Breakdown of academic impact, for papers by Hanna Mierzewska Breakdown of academic impact, for papers by John J. McMahon Breakdown of academic impact, for papers by Jean‐Baptiste Rivière Breakdown of academic impact, for papers by Jay P. Ross Breakdown of academic impact, for papers by Alysen Clark Breakdown of academic impact, for papers by Youngshin Lim Breakdown of academic impact, for papers by Vesna Ponjavic Breakdown of academic impact, for papers by Ercan Demir
Rankless by CCL
2026