Ralph Roeth

2.1k citations

19 papers · 1.2k indexed · h-index 11

Impact in

Biological Psychiatry top 2%
- Tryptophan and brain disorders
Behavioral Neuroscience top 5%
- Stress Responses and Cortisol

Papers in ⓘ

Genetics 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 3
Biological Psychiatry 1

Co-authors: Gudrun Rappold (17 shared papers)Birgit Weiß (9 shared papers)Simone Berkel (2 shared papers)Angelika Rieß (1 shared paper)Péter Szatmári (1 shared paper)Stephen W. Scherer (1 shared paper)Ute Moog (1 shared paper)Wendy Roberts (1 shared paper)
Journals: Frontiers in Endocrinology (2 papers)Frontiers in Genetics (2 papers)PLoS ONE (2 papers)Nature Genetics (1 paper)Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms (1 paper)
Partner nations: Germany United States Canada

In The Last Decade

Ralph Roeth

19 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Ralph Roeth, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ralph Roeth Line = papers co-authored together Ralph Roeth links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation Nature Genetics ·Simone Berkel, Christian R. Marshall, Birgit Weiß, Jennifer Howe, Ralph Roeth, Ute Moog, Volker Endris, Wendy Roberts, Péter Szatmári, Dalila Pinto, Michael Bonin, Angelika Rieß, Hartmut Engels, Rolf Sprengel, Stephen W. Scherer, Gudrun Rappold	2010	410
2	Microglial recruitment of IL-1β-producing monocytes to brain endothelium causes stress-induced anxiety Molecular Psychiatry ·Daniel B. McKim, Mark D. Weber, Anzela Niraula, Caroline M. Sawicki, Xuhan Liu, Brant Jarrett, Karol Ramírez, Yuchuan Wang, Ralph Roeth, Ana Sucaldito, Carly G. Sobol, Ning Quan, John F. Sheridan, Jonathan P. Godbout	2017	284
3	Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency Journal of Medical Genetics ·Gudrun Rappold, W. F. Blum, Elena P. Shavrikova, Brenda Crowe, Ralph Roeth, Charmian A. Quigley, Judith L. Ross, Beate Niesler	2006	179
4	Missense Mutations and Gene Interruption in PROSIT240 , a Novel TRAP240 -Like Gene, in Patients With Congenital Heart Defect (Transposition of the Great Arteries) Circulation ·Nadja Muncke, Christine Jung, Heinz Rüdiger, Herbert E. Ulmer, Ralph Roeth, Annette Hubert, Elizabeth Goldmuntz, Deborah A. Driscoll, Judith Goodship, Karin Schön, Gudrun Rappold	2003	116
5	Alternative Splicing and Nonsense-Mediated RNA Decay Contribute to the Regulation of SHOX Expression PLoS ONE ·Claudia Durand, Ralph Roeth, Harsh Dweep, Irena Vlatkovic, Eva L. Decker, Katja Schneider, Gudrun Rappold	2011	32
6	Investigation of SHANK3 in schizophrenia American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ana de Sena Cortabitarte, Franziska Degenhardt, Jana Strohmaier, Maren Lang, Birgit Weiß, Ralph Roeth, Ina Giegling, Stefanie Heilmann‐Heimbach, Andrea Hofmann, Dan Rujescu, Christine Fischer, Marcella Rietschel, Markus M. Nöthen, Gudrun Rappold, Simone Berkel	2017	31
7	Retinoic acid catabolizing enzyme CYP 26C1 is a genetic modifier in SHOX deficiency EMBO Molecular Medicine ·Antonino Montalbano, Lonny Juergensen, Ralph Roeth, Birgit Weiß, Maki Fukami, Susanne Fricke‐Otto, Gerhard Binder, Tsutomu Ogata, Eva L. Decker, Gudrun Nuernberg, David Hassel, Gudrun Rappold	2016	18
8	Functional Characterization of Rare Variants in the SHOX2 Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation Frontiers in Genetics ·Sandra Hoffmann, Christoph Paone, Simon Sumer, Sabrina Diebold, Birgit Weiß, Ralph Roeth, Sebastian Clauß, Ina Klier, Stefan Kääb, Andreas Schulz, Philipp S. Wild, Adil Ghrib, Tanja Zeller, Renate B. Schnabel, Steffen Just, Gudrun Rappold	2019	17
9	Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability American Journal of Medical Genetics Part A ·Christine Tyson, Angelika J. Dawson, S. Bal, M. Tomiuk, Todd J. Anderson, David Tucker, D. Riordan, Ilse Chudoba, B. Morash, Aizeddin A. Mhanni, Albert E. Chudley, Barbara McGillivray, Malcolm Parslow, Gudrun Rappold, Ralph Roeth, Chris Fawcett, Ying Qiao, Chansonette Harvard, Evica Rajcan‐Separovic	2009	14
10	Mutational analysis of the PITX2coding region revealed no common cause for transposition of the great arteries (dTGA) BMC Medical Genetics ·Nadja Muncke, Beate Niesler, Ralph Roeth, Karin Schön, Heinz-Juergen Rüdiger, Elizabeth Goldmuntz, Judith Goodship, Gudrun Rappold	2005	11
11	Functional missense and splicing variants in the retinoic acid catabolizing enzyme CYP26C1 in idiopathic short stature European Journal of Human Genetics ·Antonino Montalbano, Lonny Juergensen, Maki Fukami, Christian T. Thiel, Nadine H Hauer, Ralph Roeth, Birgit Weiß, Yasuhiro Naiki, Tsutomu Ogata, David Hassel, Gudrun Rappold	2018	11
12	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 ·Daniela Choukair, Birgit Eberle, Philipp Vick, Pia Hermanns, Birgit Weiß, Nagarajan Paramasivam, Matthias Schlesner, Katharina Lornsen, Ralph Roeth, Carina Klutmann, Jennifer Kreis, Georg F. Hoffmann, Joachim Pohlenz, Gudrun Rappold, Markus Bettendorf	2020	10
13	Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms ·Sandra Hoffmann, Stefanie Schmitteckert, Kristin Raedecke, D. Rheinert, Sabrina Diebold, Ralph Roeth, B Weiss, Martin Granzow, Beate Niesler, Anne Griesbeck, Volker Eckstein, Wolfram‐Hubertus Zimmermann, Steffen Just, Gudrun Rappold	2021	7
14	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 ·Cornelia Thoeni, Ruediger Waldherr, Jutta Scheuerer, Stefanie Schmitteckert, Ralph Roeth, Beate Niesler, Ernest Cutz, Christa Flechtenmacher, Benjamin Goeppert, Peter Schirmacher, Felix Lasitschka	2019	6
15	Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes Frontiers in Endocrinology ·Birgit Weiß, Birgit Eberle, Ralph Roeth, Christiaan de Bruin, Julian C. Lui, Nagarajan Paramasivam, Katrin Hinderhofer, Hermine A. van Duyvenvoorde, Jeffrey Baron, Jan M. Wit, Gudrun Rappold	2021	5
16	The Homeobox Transcription Factor HOXA9 Is a Regulator of SHOX in U2OS Cells and Chicken Micromass Cultures PLoS ONE ·Claudia Durand, Eva L. Decker, Ralph Roeth, Katja Schneider, Gudrun Rappold	2012	4
17	Identification and Tissue-Specific Characterization of Novel SHOX-Regulated Genes in Zebrafish Highlights SOX Family Members Among Other Genes Frontiers in Genetics ·Sandra Hoffmann, Ralph Roeth, Sabrina Diebold, Jasmin Gogel, David Hassel, Steffen Just, Gudrun Rappold	2021	4
18	Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism Genes ·Philipp Vick, Birgit Eberle, Daniela Choukair, Birgit Weiß, Ralph Roeth, Isabelle Schneider, Nagarajan Paramasivam, Markus Bettendorf, Gudrun Rappold	2021	2
19	Identification of novel genes including NAV2 associated with isolated tall stature Frontiers in Endocrinology ·Birgit Weiß, Tim Ott, Philipp Vick, Julian C. Lui, Ralph Roeth, Sebastian Vogel, Stephan Waldmüller, Sandra Hoffmann, Jeffrey Baron, Jan M. Wit, Gudrun Rappold	2023	1

About Ralph Roeth

Ralph Roeth is a scholar working on Genetics, Biological Psychiatry, Behavioral Neuroscience, Developmental Neuroscience and Immunology, having authored 19 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (4 papers), interferon and immune responses (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Thyroid Disorders and Treatments (2 papers), Autism Spectrum Disorder Research (2 papers) and Retinoids in leukemia and cellular processes (2 papers). The work is most often cited by research in Biological Psychiatry (190 citations), Behavioral Neuroscience (159 citations), Genetics (573 citations), Neurology (163 citations) and Cognitive Neuroscience (253 citations). Ralph Roeth has collaborated with scholars based in Germany, United States and Canada. Frequent co-authors include Gudrun Rappold, Birgit Weiß, Simone Berkel, Angelika Rieß, Péter Szatmári, Stephen W. Scherer, Ute Moog, Wendy Roberts, Hartmut Engels and Michael Bonin. Their work appears in journals such as Frontiers in Endocrinology, Frontiers in Genetics, PLoS ONE, Nature Genetics and Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms.

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