Juliane Ramser

32.3k total citations
54 papers, 1.8k citations indexed

About

Juliane Ramser is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Juliane Ramser has authored 54 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 22 papers in Genetics and 9 papers in Oncology. Recurrent topics in Juliane Ramser's work include RNA and protein synthesis mechanisms (7 papers), BRCA gene mutations in cancer (6 papers) and Cancer Genomics and Diagnostics (6 papers). Juliane Ramser is often cited by papers focused on RNA and protein synthesis mechanisms (7 papers), BRCA gene mutations in cancer (6 papers) and Cancer Genomics and Diagnostics (6 papers). Juliane Ramser collaborates with scholars based in Germany, United States and United Kingdom. Juliane Ramser's co-authors include Kurt Weising, Günter Kahl, Alfons Meindl, Annette Jansson, Heide Hellebrand, K. Schneider, Ellen D. Renner, Miroslav Habán, J Diébold and Veit Grote and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Juliane Ramser

54 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Juliane Ramser Germany	20	934	472	376	376	240	54	1.8k
Stefan Vinckier Belgium	26	1.1k 1.2×	101 0.2×	90 0.2×	136 0.4×	279 1.2×	53	2.0k
Ellen S. Regalado United States	30	526 0.6×	371 0.8×	1.4k 3.6×	308 0.8×	251 1.0×	58	2.7k
Naohiro Hashimoto Japan	23	1.5k 1.6×	100 0.2×	278 0.7×	254 0.7×	112 0.5×	55	2.3k
Nathalie Clément United States	28	1.4k 1.5×	143 0.3×	1.1k 3.0×	79 0.2×	27 0.1×	72	2.3k
Shinji Matsumoto Japan	25	1.5k 1.6×	80 0.2×	168 0.4×	169 0.4×	86 0.4×	71	2.0k
Helia B. Schönthaler Switzerland	19	949 1.0×	87 0.2×	119 0.3×	56 0.1×	64 0.3×	22	1.9k
Katrina Rothblum United States	20	1.2k 1.2×	100 0.2×	198 0.5×	119 0.3×	48 0.2×	28	1.8k
Marianthi Kiriakidou United States	23	2.3k 2.4×	537 1.1×	686 1.8×	151 0.4×	117 0.5×	27	3.8k
Bradley Rosenzweig United States	12	1.1k 1.2×	93 0.2×	127 0.3×	61 0.2×	131 0.5×	12	1.5k
Gabrielle S. Sellick United Kingdom	22	762 0.8×	90 0.2×	610 1.6×	273 0.7×	34 0.1×	40	1.6k

Countries citing papers authored by Juliane Ramser

Since Specialization

Citations

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

Fields of papers citing papers by Juliane Ramser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juliane Ramser

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

Lange, Sebastian, H. Carlo Maurer, Kenneth P. Olive, et al.. (2021). PALLD mutation in a European family conveys a stromal predisposition for familial pancreatic cancer. JCI Insight. 6(8). 7 indexed citations

Hauke, Jan, Barbara Wappenschmidt, Ulrike Faust, et al.. (2021). Aktualisierte Kriterien des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zur Klassifizierung von Keimbahn-Sequenzvarianten in Risikogenen für familiären Brust- und Eierstockkrebs. Senologie - Zeitschrift für Mammadiagnostik und -therapie. 18(2). 136–162. 3 indexed citations

Grill, Sabine, Juliane Ramser, Heide Hellebrand, et al.. (2020). TP53 germline mutations in the context of families with hereditary breast and ovarian cancer: a clinical challenge. Archives of Gynecology and Obstetrics. 303(6). 1557–1567. 6 indexed citations

Wappenschmidt, Barbara, Jan Hauke, Ulrike Faust, et al.. (2020). Criteria of the German Consortium for Hereditary Breast and Ovarian Cancer for the Classification of Germline Sequence Variants in Risk Genes for Hereditary Breast and Ovarian Cancer. Geburtshilfe und Frauenheilkunde. 80(4). 410–429. 14 indexed citations

Meindl, A, Juliane Ramser, Jan Hauke, & Eric Hahnen. (2015). Genetic aspects of hereditary breast and ovarian cancer: options and limits. Kölner Universitäts PublikationsServer (Universität zu Köln). 1 indexed citations

Klein, Andreas, Christian Olendrowitz, Juergen A. Hampl, et al.. (2008). Identification of brain- and bone-specific breast cancer metastasis genes. Cancer Letters. 276(2). 212–220. 88 indexed citations

Martínez‐Garay, Isabel, Miguel Tomás Vila, Silvestre Oltra, et al.. (2006). A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. European Journal of Human Genetics. 15(1). 29–34. 28 indexed citations

Ramser, Juliane, Fatima Abidi, Céline Burcklé, et al.. (2005). A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. Human Molecular Genetics. 14(8). 1019–1027. 146 indexed citations

Wen, Gaiping, Juliane Ramser, Stefan Taudien, et al.. (2005). Validation of mRNA/EST-based gene predictions in human Xp11.4 revealed differences to the organization of the orthologous mouse locus. Mammalian Genome. 16(12). 934–941. 1 indexed citations

10.

Ramser, Juliane, et al.. (2004). A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9). Journal of Medical Genetics. 41(9). 679–683. 51 indexed citations

11.

Golla, Astrid, Annette Jansson, Juliane Ramser, et al.. (2002). Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22. European Journal of Human Genetics. 10(3). 217–221. 130 indexed citations

12.

Demirci, F. Yesim, Brian W. Rigatti, Gaiping Wen, et al.. (2002). X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15. The American Journal of Human Genetics. 70(4). 1049–1053. 138 indexed citations

13.

Thiselton, Dawn L., Jennifer McDowall, Oliver Brandau, et al.. (2002). An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders. Genomics. 79(4). 560–572. 72 indexed citations

14.

Valadez‐Moctezuma, Ernestina, et al.. (2001). Técnicas moleculares para la caracterización de genomas vegetales (garbanzo) y algunas aplicaciones potenciales. LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas). 3 indexed citations

15.

Kirschner‐Schwabe, Renate, Christina Zeitz, Juliane Ramser, et al.. (2001). DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements. Human Genetics. 109(3). 271–278. 15 indexed citations

16.

Pusch, Carsten M., Johannes Maurer, Juliane Ramser, et al.. (2001). Complete form of X-linked congenital stationary night blindness: Refined mapping and evidence of genetic homogeneity. International Journal of Molecular Medicine. 7(2). 155–61. 2 indexed citations

17.

Radelof, Uwe, Steffen Hennig, Juliane Ramser, et al.. (1998). Preselection of shotgun clones by oligonucleotide fingerprinting: an efficient and high throughput strategy to reduce redundancy in large-scale sequencing projects. Nucleic Acids Research. 26(23). 5358–5364. 29 indexed citations

18.

Ramser, Juliane, A. R. Villanueva, & Harold M. Frost. (1966). Cortical Bone Dynamics in Osteomalacia, Measured by Tetracycline Bone-labeling. Clinical Orthopaedics and Related Research. 49(1). 89???102–89???102. 14 indexed citations

19.

Ramser, Juliane, Harold M. Frost, Boy Frame, Alfred Arnstein, & Roger Smith. (1966). 20 Tetracycline-Based Studies of Bone Dynamics in Rib of 6 Cases of Osteomalacia. Clinical Orthopaedics and Related Research. 46. 219–238. 9 indexed citations

20.

Ramser, Juliane, Harold M. Frost, & Roger Smith. (1966). Tetracycline-Based Measurement of the Tissue and Cell Dynamics in Rib of a 25-Year-Old Man With Active Acromegaly. Clinical Orthopaedics and Related Research. 49(1). 169???172–169???172. 8 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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