Rami Abou Jamra

9.9k total citations
99 papers, 2.8k citations indexed

About

Rami Abou Jamra is a scholar working on Genetics, Molecular Biology and Biochemistry. According to data from OpenAlex, Rami Abou Jamra has authored 99 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 62 papers in Molecular Biology and 11 papers in Biochemistry. Recurrent topics in Rami Abou Jamra's work include Genetics and Neurodevelopmental Disorders (37 papers), Genomics and Rare Diseases (27 papers) and Genomic variations and chromosomal abnormalities (15 papers). Rami Abou Jamra is often cited by papers focused on Genetics and Neurodevelopmental Disorders (37 papers), Genomics and Rare Diseases (27 papers) and Genomic variations and chromosomal abnormalities (15 papers). Rami Abou Jamra collaborates with scholars based in Germany, United States and Netherlands. Rami Abou Jamra's co-authors include Markus M. Nöthen, Sven Cichon, Marcella Rietschel, Peter Propping, Thomas G. Schulze, André Reis, Susanne Höfels, Arif B. Ekici, Rebecca Buchert and Alexander Georgi and has published in prestigious journals such as Nature Communications, Molecular and Cellular Biology and Brain.

In The Last Decade

Rami Abou Jamra

95 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rami Abou Jamra Germany 29 1.4k 1.1k 544 407 317 99 2.8k
Tomoko Toyota Japan 31 1.5k 1.1× 850 0.8× 818 1.5× 344 0.8× 192 0.6× 87 2.8k
Nadine Norton United Kingdom 45 2.8k 2.0× 2.2k 2.0× 1.1k 2.0× 832 2.0× 198 0.6× 108 5.9k
Koko Ishizuka United States 21 1.4k 1.0× 431 0.4× 714 1.3× 218 0.5× 144 0.5× 59 2.5k
Rikke S. Møller Denmark 28 1.0k 0.8× 1.3k 1.2× 426 0.8× 792 1.9× 100 0.3× 121 2.4k
Paul R. Buckland United Kingdom 35 1.6k 1.1× 1.0k 0.9× 1.1k 1.9× 422 1.0× 128 0.4× 82 3.3k
Dawn L. Thiselton United States 24 2.0k 1.5× 575 0.5× 413 0.8× 146 0.4× 162 0.5× 56 2.9k
Steven J. Clapcote United Kingdom 25 1.5k 1.1× 574 0.5× 806 1.5× 216 0.5× 109 0.3× 49 2.5k
Tetsuo Ohnishi Japan 24 2.1k 1.5× 409 0.4× 510 0.9× 146 0.4× 344 1.1× 74 3.0k
Anna Fassio Italy 29 1.3k 1.0× 463 0.4× 979 1.8× 242 0.6× 850 2.7× 56 2.4k
Ben Pickard United Kingdom 29 2.0k 1.5× 1.1k 1.0× 439 0.8× 259 0.6× 73 0.2× 58 2.9k

Countries citing papers authored by Rami Abou Jamra

Since Specialization
Citations

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

Fields of papers citing papers by Rami Abou Jamra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rami Abou Jamra. 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 Rami Abou Jamra. The network helps show where Rami Abou Jamra may publish in the future.

Co-authorship network of co-authors of Rami Abou Jamra

This figure shows the co-authorship network connecting the top 25 collaborators of Rami Abou Jamra. A scholar is included among the top collaborators of Rami Abou Jamra 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 Rami Abou Jamra. Rami Abou Jamra 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.
Faust, H., Matthias Blüher, Antje Körner, et al.. (2025). Detecting monogenic obesity: a systematic exome-wide workup of over 500 individuals. International Journal of Obesity. 49(7). 1400–1411.
2.
Koch‐Hogrebe, Margarete, Claudia Roll, Axel Panzer, et al.. (2024). A Rapid Onset and Fatal Disease Course in a 17-Year-Old Boy with Vanishing White Matter Disease (VWM) Triggered by RSV Infection. Neuropediatrics. 55(S 01). S1–S25.
3.
Bergner, Caroline G., Marjolein Breur, Julia Lier, et al.. (2024). Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy. Brain. 147(10). 3562–3572. 4 indexed citations
4.
Wolf, Christine, Jörn‐Sven Kühl, Sarah Koss, et al.. (2023). Hemophagocytic lymphohistiocytosis–like hyperinflammation due to a de novo mutation in DPP9. Journal of Allergy and Clinical Immunology. 152(5). 1336–1344.e5. 5 indexed citations
5.
Averdunk, Luisa, Khalid Al‐Thihli, Harald Surowy, et al.. (2022). Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain. Clinical Genetics. 103(4). 484–491. 1 indexed citations
6.
Landgraf, Kathrin, Robert Stein, Anja Hilbert, et al.. (2022). Aberrant expression of agouti signaling protein (ASIP) as a cause of monogenic severe childhood obesity. Nature Metabolism. 4(12). 1697–1712. 17 indexed citations
7.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
8.
Popp, Bernt, Melanie Brügger, Tobias Bartolomaeus, et al.. (2022). The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical Genetics. 103(2). 226–230. 2 indexed citations
9.
Krohn, Knut, Diana Le Duc, Mathias A. Böhme, et al.. (2022). Improving one-step scarless genome editing in Drosophila melanogaster by combining ovoD co-CRISPR selection with sgRNA target site masking. Biology Methods and Protocols. 7(1). bpac003–bpac003.
10.
Jamra, Rami Abou, et al.. (2022). Routine Diagnostics Confirm Novel Neurodevelopmental Disorders. Genes. 13(12). 2305–2305. 5 indexed citations
11.
Platzer, Konrad, Heinrich Sticht, Caleb Bupp, et al.. (2022). De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission. Annals of Neurology. 92(6). 958–973. 12 indexed citations
12.
Roth, Christian, et al.. (2021). Congenital cervical spine malformation due to bi‐allelic RIPPLY2 variants in spondylocostal dysostosis type 6. Clinical Genetics. 99(4). 565–571. 3 indexed citations
13.
Zacher, Pia, Tobias Bartolomaeus, Diana Le Duc, et al.. (2021). The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals. Genetics in Medicine. 23(8). 1492–1497. 31 indexed citations
14.
Jamra, Rami Abou, Arndt Borkhardt, Triantafyllia Brozou, et al.. (2020). QRICH1 variants in Ververi‐Brady syndrome—delineation of the genotypic and phenotypic spectrum. Clinical Genetics. 99(1). 199–207. 6 indexed citations
15.
Fagerberg, Christina, Adrian Taylor, Felix Distelmaier, et al.. (2019). Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration. Brain. 143(1). 94–111. 18 indexed citations
16.
Maier, Oliver, Holger Rehmann, Maarten H. Lequin, et al.. (2018). Identification of a Loss-of-Function Mutation in the Context of Glutaminase Deficiency and Neonatal Epileptic Encephalopathy. JAMA Neurology. 76(3). 342–342. 34 indexed citations
17.
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
18.
Nieratschker, Vanessa, Josef Frank, Thomas W. Mühleisen, et al.. (2010). The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample. Schizophrenia Research. 122(1-3). 24–30. 20 indexed citations
19.
Schumacher, Johannes, Rami Abou Jamra, Tim Becker, et al.. (2005). Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression. Biological Psychiatry. 58(4). 307–314. 247 indexed citations
20.
Jamra, Rami Abou, Johannes Schumacher, Astrid Golla, et al.. (2003). Family‐based association studies of α‐adrenergic receptor genes in chromosomal regions with linkage to bipolar affective disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 126B(1). 79–81. 5 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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