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Entries: 1-10  
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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  
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