Ralph Roeth

2.1k total citations
19 papers, 1.2k citations indexed

About

Ralph Roeth is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Ralph Roeth has authored 19 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 4 papers in Immunology. Recurrent topics in Ralph Roeth's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Ralph Roeth is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Congenital heart defects research (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Ralph Roeth collaborates with scholars based in Germany, United States and Canada. Ralph Roeth's co-authors include Gudrun Rappold, Birgit Weiß, Simone Berkel, Péter Szatmári, Angelika Rieß, Volker Endris, Stephen W. Scherer, Rolf Sprengel, Jennifer Howe and Michael Bonin and has published in prestigious journals such as Circulation, Nature Genetics and PLoS ONE.

In The Last Decade

Ralph Roeth

19 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralph Roeth Germany 11 573 545 253 190 163 19 1.2k
Mira Jakovcevski Germany 22 442 0.8× 1.2k 2.1× 162 0.6× 114 0.6× 74 0.5× 35 1.8k
Ciara Fahey Ireland 19 286 0.5× 572 1.0× 254 1.0× 95 0.5× 52 0.3× 25 1.2k
Hongen Wei China 17 415 0.7× 376 0.7× 513 2.0× 98 0.5× 161 1.0× 32 1.2k
John D. H. Stead Canada 19 244 0.4× 455 0.8× 100 0.4× 187 1.0× 69 0.4× 25 1.3k
Kathrin Nickel Germany 19 180 0.3× 204 0.4× 399 1.6× 210 1.1× 122 0.7× 85 1.2k
Galit Shaltiel Israel 18 240 0.4× 535 1.0× 107 0.4× 142 0.7× 56 0.3× 29 1.2k
Annie Vogel Ciernia United States 20 403 0.7× 689 1.3× 436 1.7× 68 0.4× 199 1.2× 34 1.5k
Rosalba Satta United States 14 346 0.6× 693 1.3× 117 0.5× 163 0.9× 33 0.2× 16 1.1k
Paweł Kapelski Poland 20 285 0.5× 351 0.6× 302 1.2× 222 1.2× 31 0.2× 66 1.2k
Sagar D. Patel United States 8 319 0.6× 385 0.7× 94 0.4× 177 0.9× 24 0.1× 11 968

Countries citing papers authored by Ralph Roeth

Since Specialization
Citations

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

Fields of papers citing papers by Ralph Roeth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralph Roeth

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

All Works

19 of 19 papers shown
1.
Weiß, Birgit, Tim Ott, Philipp Vick, et al.. (2023). Identification of novel genes including NAV2 associated with isolated tall stature. Frontiers in Endocrinology. 14. 1258313–1258313. 1 indexed citations
2.
Weiß, Birgit, Ralph Roeth, Christiaan de Bruin, et al.. (2021). Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes. Frontiers in Endocrinology. 12. 660731–660731. 5 indexed citations
3.
Vick, Philipp, Daniela Choukair, Birgit Weiß, et al.. (2021). Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism. Genes. 12(12). 1862–1862. 2 indexed citations
4.
Hoffmann, Sandra, Stefanie Schmitteckert, Ralph Roeth, et al.. (2021). Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1864(4-5). 194702–194702. 7 indexed citations
5.
6.
Choukair, Daniela, Philipp Vick, Pia Hermanns, et al.. (2020). Identification of <b><i>Transient Receptor Potential Channel 4-Associated Protein</i></b> as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism. Hormone Research in Paediatrics. 93(1). 16–29. 10 indexed citations
7.
Hoffmann, Sandra, Birgit Weiß, Ralph Roeth, et al.. (2019). Functional Characterization of Rare Variants in the SHOX2 Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation. Frontiers in Genetics. 10. 648–648. 17 indexed citations
8.
Thoeni, Cornelia, Ruediger Waldherr, Stefanie Schmitteckert, et al.. (2019). Expression Analysis of ATP-Binding Cassette Transporters ABCB11 and ABCB4 in Primary Sclerosing Cholangitis and Variety of Pediatric and Adult Cholestatic and Noncholestatic Liver Diseases. Canadian Journal of Gastroenterology and Hepatology. 2019. 1–10. 6 indexed citations
9.
Montalbano, Antonino, Maki Fukami, Christian T. Thiel, et al.. (2018). Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature. European Journal of Human Genetics. 26(8). 1113–1120. 11 indexed citations
10.
McKim, Daniel B., Mark D. Weber, Anzela Niraula, et al.. (2017). Microglial recruitment of IL-1β-producing monocytes to brain endothelium causes stress-induced anxiety. Molecular Psychiatry. 23(6). 1421–1431. 284 indexed citations
11.
Degenhardt, Franziska, Jana Strohmaier, Maren Lang, et al.. (2017). Investigation of SHANK3 in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(4). 390–398. 31 indexed citations
12.
Montalbano, Antonino, Ralph Roeth, Birgit Weiß, et al.. (2016). Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency. EMBO Molecular Medicine. 8(12). 1455–1469. 18 indexed citations
13.
Decker, Eva L., et al.. (2012). The Homeobox Transcription Factor HOXA9 Is a Regulator of SHOX in U2OS Cells and Chicken Micromass Cultures. PLoS ONE. 7(9). e45369–e45369. 4 indexed citations
14.
Roeth, Ralph, Harsh Dweep, Irena Vlatkovic, et al.. (2011). Alternative Splicing and Nonsense-Mediated RNA Decay Contribute to the Regulation of SHOX Expression. PLoS ONE. 6(3). e18115–e18115. 32 indexed citations
15.
Berkel, Simone, Christian R. Marshall, Birgit Weiß, et al.. (2010). Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nature Genetics. 42(6). 489–491. 410 indexed citations
16.
Tyson, Christine, Angelika J. Dawson, Todd J. Anderson, et al.. (2009). Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability. American Journal of Medical Genetics Part A. 149A(3). 490–495. 14 indexed citations
17.
Rappold, Gudrun, W. F. Blum, Elena P. Shavrikova, et al.. (2006). Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency. Journal of Medical Genetics. 44(5). 306–313. 179 indexed citations
18.
Niesler, Beate, Ralph Roeth, Karin Schön, et al.. (2005). Mutational analysis of the PITX2coding region revealed no common cause for transposition of the great arteries (dTGA). BMC Medical Genetics. 6(1). 20–20. 11 indexed citations
19.
Jung, Christine, Heinz Rüdiger, Herbert E. Ulmer, et al.. (2003). Missense Mutations and Gene Interruption in PROSIT240 , a Novel TRAP240 -Like Gene, in Patients With Congenital Heart Defect (Transposition of the Great Arteries). Circulation. 108(23). 2843–2850. 116 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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