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Institution

Martin Luther University of Halle-Wittenberg

EducationHalle, Germany
About: Martin Luther University of Halle-Wittenberg is a education organization based out in Halle, Germany. It is known for research contribution in the topics: Population & Liquid crystal. The organization has 20232 authors who have published 38773 publications receiving 965004 citations. The organization is also known as: MLU & University of Wittenberg.


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Journal ArticleDOI
Antonio F. Pardiñas1, Peter Holmans1, Andrew Pocklington1, Valentina Escott-Price1, Stephan Ripke2, Stephan Ripke3, Noa Carrera1, Sophie E. Legge1, Sophie Bishop1, D. F. Cameron1, Marian L. Hamshere1, Jun Han1, Leon Hubbard1, Amy Lynham1, Kiran Kumar Mantripragada1, Elliott Rees1, James H. MacCabe4, Steven A. McCarroll5, Bernhard T. Baune6, Gerome Breen4, Gerome Breen7, Enda M. Byrne8, Udo Dannlowski9, Thalia C. Eley4, Caroline Hayward10, Nicholas G. Martin8, Nicholas G. Martin11, Andrew M. McIntosh10, Robert Plomin4, David J. Porteous10, Naomi R. Wray8, Armando Caballero12, Daniel H. Geschwind13, Laura M. Huckins14, Douglas M. Ruderfer14, Enrique Santiago15, Pamela Sklar14, Eli A. Stahl14, Hyejung Won13, Esben Agerbo16, Esben Agerbo17, Thomas Damm Als16, Thomas Damm Als17, Ole A. Andreassen18, Ole A. Andreassen19, Marie Bækvad-Hansen20, Marie Bækvad-Hansen17, Preben Bo Mortensen16, Preben Bo Mortensen17, Carsten Bøcker Pedersen17, Carsten Bøcker Pedersen16, Anders D. Børglum16, Anders D. Børglum17, Jonas Bybjerg-Grauholm20, Jonas Bybjerg-Grauholm17, Srdjan Djurovic21, Srdjan Djurovic18, Naser Durmishi, Marianne Giørtz Pedersen16, Marianne Giørtz Pedersen17, Vera Golimbet, Jakob Grove, David M. Hougaard17, David M. Hougaard20, Manuel Mattheisen17, Manuel Mattheisen16, Espen Molden, Ole Mors22, Ole Mors17, Merete Nordentoft23, Merete Nordentoft17, Milica Pejovic-Milovancevic24, Engilbert Sigurdsson, Teimuraz Silagadze25, Christine Søholm Hansen17, Christine Søholm Hansen20, Kari Stefansson26, Hreinn Stefansson26, Stacy Steinberg26, Sarah Tosato27, Thomas Werge28, Thomas Werge17, Thomas Werge23, David A. Collier4, David A. Collier29, Dan Rujescu30, Dan Rujescu31, George Kirov1, Michael J. Owen1, Michael Conlon O'Donovan1, James T.R. Walters1 
TL;DR: A new genome-wide association study of schizophrenia is reported, and through meta-analysis with existing data and integrating genomic fine-mapping with brain expression and chromosome conformation data, 50 novel associated loci and 145 loci are identified.
Abstract: Schizophrenia is a debilitating psychiatric condition often associated with poor quality of life and decreased life expectancy. Lack of progress in improving treatment outcomes has been attributed to limited knowledge of the underlying biology, although large-scale genomic studies have begun to provide insights. We report a new genome-wide association study of schizophrenia (11,260 cases and 24,542 controls), and through meta-analysis with existing data we identify 50 novel associated loci and 145 loci in total. Through integrating genomic fine-mapping with brain expression and chromosome conformation data, we identify candidate causal genes within 33 loci. We also show for the first time that the common variant association signal is highly enriched among genes that are under strong selective pressures. These findings provide new insights into the biology and genetic architecture of schizophrenia, highlight the importance of mutation-intolerant genes and suggest a mechanism by which common risk variants persist in the population.

1,259 citations

Journal ArticleDOI
24 Apr 2008-Nature
TL;DR: Tribolium castaneum is a member of the most species-rich eukaryotic order, a powerful model organism for the study of generalized insect development, and an important pest of stored agricultural products.
Abstract: Tribolium castaneum is a member of the most species-rich eukaryotic order, a powerful model organism for the study of generalized insect development, and an important pest of stored agricultural products. We describe its genome sequence here. This omnivorous beetle has evolved the ability to interact with a diverse chemical environment, as shown by large expansions in odorant and gustatory receptors, as well as P450 and other detoxification enzymes. Development in Tribolium is more representative of other insects than is Drosophila, a fact reflected in gene content and function. For example, Tribolium has retained more ancestral genes involved in cell-cell communication than Drosophila, some being expressed in the growth zone crucial for axial elongation in short-germ development. Systemic RNA interference in T. castaneum functions differently from that in Caenorhabditis elegans, but nevertheless offers similar power for the elucidation of gene function and identification of targets for selective insect control.

1,248 citations

Journal ArticleDOI
TL;DR: Almost one fourth of patients with apparently sporadic pheochromocytoma may be carriers of mutations; routine analysis for mutations of RET, VHL, SDHD, and SDHB is indicated to identify pheosene-associated syndromes that would otherwise be missed.
Abstract: Background The group of susceptibility genes for pheochromocytoma that included the proto-oncogene RET (associated with multiple endocrine neoplasia type 2 [MEN-2]) and the tumor-suppressor gene VHL (associated with von Hippel–Lindau disease) now also encompasses the newly identified genes for succinate dehydrogenase subunit D (SDHD) and succinate dehydrogenase subunit B (SDHB), which predispose carriers to pheochromocytomas and glomus tumors. We used molecular tools to classify a large cohort of patients with pheochromocytoma with respect to the presence or absence of mutations of one of these four genes and to investigate the relevance of genetic analyses to clinical practice. Methods Peripheral blood from unrelated, consenting registry patients with pheochromocytoma was tested for mutations of RET, VHL, SDHD, and SDHB. Clinical data at first presentation and follow-up were evaluated. Results Among 271 patients who presented with nonsyndromic pheochromocytoma and without a family history of the disease,...

1,228 citations

Journal ArticleDOI
24 Nov 2004-Cell
TL;DR: A model is proposed whereby SNP309 serves as a rate-limiting event in carcinogenesis, and a single nucleotide polymorphism (SNP309) is found in the MDM2 promoter and is shown to increase the affinity of the transcriptional activator Sp1, resulting in higher levels ofMDM2 RNA and protein and the subsequent attenuation of the p53 pathway.

1,226 citations


Authors

Showing all 20466 results

NameH-indexPapersCitations
Niels Birbaumer14283577853
Michael Schmitt1342007114667
Niels E. Skakkebæk12759659925
Stefan D. Anker117415104945
Pedro W. Crous11580951925
Eric Verdin11537047971
Bernd Nilius11249644812
Josep Tabernero11180368982
Hans-Dieter Volk10778446622
Dan Rujescu10655260406
John I. Nurnberger10552251402
Ulrich Gösele10260346223
Wolfgang J. Parak10246943307
Martin F. Bachmann10041534124
Munir Pirmohamed9767539822
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202397
2022331
20212,038
20202,007
20191,617
20181,604