Please note that eDoc will be permanently shut down in the first quarter of 2021!      Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Home
Search
Quick Search
Advanced
Fulltext
Browse
Collections
Persons
My eDoc
Session History
Login
Name:
Password:
Documentation
Help
Support Wiki
Direct access to
document ID:


          Display Documents


Institute:
Collection:
Print in Citation style Print version     Display:
Sort by: Display records with Fulltext only
Entries: 1-10  
 Basket 
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
Authors: Winkelmann, J.; Czamara, D.; Schormair, B.; Knauf, F.; Schulte, E. C.; Trenkwalder, C.; Dauvilliers, Y.; Polo, O.; Högl, B.; Berger, K.; Fuhs, A.; Gross, N.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Xiong, L.; Montplaisir, J.; Rouleau, G. A.; Fietze, I.; Vavrova, J.; Kemlink, D.; Sonka, K.; Nevsimalova, S.; Lin, S. C.; Wszolek, Z.; Vilarino-Guell, C.; Farrer, M. J.; Gschliesser, V.; Frauscher, B.; Falkenstetter, T.; Poewe, W.; Allen, R. P.; Earley, C. J.; Ondo, W. G.; Le, W. D.; Spieler, D.; Kaffe, M.; Zimprich, A.; Kettunen, J.; Perola, M.; Silander, K.; Cournu-Rebeix, I.; Francavilla, M.; Fontenille, C.; Fontaine, B.; Vodicka, P.; Prokisch, H.; Lichtner, P.; Peppard, P.; Faraco, J.; Mignot, E.; Gieger, C.; Illig, T.; Wichmann, H. E.; Müller-Myhsok, B.; Meitinger, T.
Date of Publication (YYYY-MM-DD): 2011-07
Title of Journal: PLoS Genetics
Volume: 7
Issue / Number: 7
Sequence Number of Article: e1002171
Document Type: Article
ID: 571350.0
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels
Authors: Oexle, K.; Ried, J. S.; Hicks, A. A.; Tanaka, T.; Hayward, C.; Bruegel, M.; Gögele, M.; Lichtner, P.; Müller-Myhsok, B.; Döring, A.; Illig, T.; Schwienbacher, C.; Minelli, C.; Pichler, I.; Fiedler, G. M.; Thiery, J.; Rudan, I.; Wright, A. F.; Campbell, H.; Ferrucci, L.; Bandinelli, S.; Pramstaller, P. P.; Wichmann, H. E.; Gieger, C.; Winkelmann, J.; Meitinger, T.
Date of Publication (YYYY-MM-DD): 2011-03-01
Title of Journal: Human Molecular Genetics
Volume: 20
Issue / Number: 5
Start Page: 1042
End Page: 1047
Document Type: Article
ID: 536123.0
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Authors: Horn, D.; Kapeller, J.; Rivera-Brugues, N.; Moog, U.; Lorenz-Depiereux, B.; Eck, S.; Hempel, M.; Wagenstaller, J.; Gawthrope, A.; Monaco, A. P.; Bonin, M.; Riess, O.; Wohlleber, E.; Illig, T.; Bezzina, C. R.; Franke, A.; Spranger, S.; Villavicencio-Lorini, P.; Seifert, W.; Rosenfeld, J.; Klopocki, E.; Rappold, G. A.; Strom, T. M.
Date of Publication (YYYY-MM-DD): 2010-11-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 11
Start Page: E1851
End Page: E1860
Document Type: Article
ID: 539476.0
 
Full text / Content available
Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
Authors: Hemminki, K.; Müller-Myhsok, B.; Lichtner, P.; Engel, C.; Chen, B. W.; Burwinkel, B.; Försti, A.; Sutter, C.; Wappenschmidt, B.; Hellebrand, H.; Illig, T.; Arnold, N.; Niederacher, D.; Dworniczak, B.; Deissler, H.; Kast, K.; Gadzicki, D.; Meitinger, T.; Wichmann, H. E.; Kiechle, M.; Bartram, C. R.; Schmutzler, R. K.; Meindl, A.
Date of Publication (YYYY-MM-DD): 2010-06-15
Title of Journal: International Journal of Cancer
Volume: 126
Issue / Number: 12
Start Page: 2858
End Page: 2862
Document Type: Article
ID: 477353.0
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany
Authors: Luecking, C. B.; Lichtner, P.; Kramer, E. R.; Gieger, C.; Illig, T.; Dichgans, M.; Berg, D.; Gasser, T.
Date of Publication (YYYY-MM-DD): 2010-01
Title of Journal: Neurobiology of Aging
Volume: 31
Issue / Number: 1
Start Page: 167
End Page: 168
Document Type: Article
ID: 440939.0
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis
Authors: Fernandez-Santiago, R.; Hoenig, S.; Lichtner, P.; Sperfeld, A. D.; Sharma, M.; Berg, D.; Weichenrieder, O.; Illig, T.; Eger, K.; Meyer, T.; Anneser, J.; Münch, C.; Zierz, S.; Gasser, T.; Ludolph, A.
Date of Publication (YYYY-MM-DD): 2009-08
Title of Journal: J Neurol
Volume: 256
Issue / Number: 8
Start Page: 1337
End Page: 1342
Document Type: Article
ID: 460591.0
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Authors: Schormair, B.; Kemlink, D.; Roeske, D.; Eckstein, G.; Xiong, L.; Lichtner, P.; Ripke, S.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Högl, B.; Frauscher, B.; Gschliesser, V.; Poewe, W.; Peglau, I.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, H. E.; Holsboer, F.; Mueller-Myhsok, B.; Meitinger, T.; Winkelmann, J.
Date of Publication (YYYY-MM-DD): 2008-08
Title of Journal: Nature Genetics
Volume: 40
Issue / Number: 8
Start Page: 946
End Page: 948
Document Type: Article
ID: 379927.0
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome
Authors: Winkelmann, J.; Lichtner, P.; Schormair, B.; Uhr, M.; Hauk, S.; Stiasny-Kolster, K.; Trenkwalder, C.; Paulus, W.; Peclau, I.; Eisensehr, I.; Illig, T.; Wichmann, H. E.; Pfister, H.; Golic, J.; Bettecken, T.; Pütz, B.; Holsboer, F.; Meitinger, T.; Müller-Myhsok, B.
Date of Publication (YYYY-MM-DD): 2008-02-15
Title of Journal: Movement Disorders
Volume: 23
Issue / Number: 3
Start Page: 350
End Page: 358
Document Type: Article
ID: 359396.0
 
Full text / Content available
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations
Authors: Sedlacek, K.; Neureuther, K.; Mueller, J. C.; Stark, K.; Fischer, M.; Baessler, A.; Reinhard, W.; Broeckel, U.; Lieb, W.; Erdmann, J.; Schunkert, H.; Riegger, G.; Illig, T.; Meitinger, T.; Hengstenberg, C.
Date of Publication (YYYY-MM-DD): 2007-09
Title of Journal: Journal of Molecular Medicine-JMM
Volume: 85
Issue / Number: 9
Start Page: 997
End Page: 1004
Document Type: Article
ID: 345083.0
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
Authors: Winkelmann, J.; Schormair, B.; Lichtner, P.; Ripke, S.; Xiong, L.; Jalilzadeh, S.; Fulda, S.; Pütz, B.; Eckstein, G.; Hauk, S.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Peglau, I.; Eisensehr, I.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, E.; Holsboer, F.; Müller-Myhsok, B.; Meitinger, T.
Date of Publication (YYYY-MM-DD): 2007-08
Title of Journal: Nature Genetics
Volume: 39
Issue / Number: 8
Start Page: 1000
End Page: 1006
Document Type: Article
ID: 334282.0
Entries: 1-10  
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.