Publikationen 2010

Humangenetik

Direktor:
Prof. Dr. med. André Reis

Publikationen 2010

  • Goecke TW, Ekici AB, Niesler B, Loehberg CR, Hammer C, Rappold G, Schanze D, Straub V, Altmann HH, Strissel P, Strick R, Beckmann MW, Fasching PA: (2010) Two naturally occurring variants of the serotonin receptor gene HTR3C are...
    Acta Obstet Gynecol Scand. 2010;89(1): 7-14
  • Smigiel R, Bednarczyk D, Laczmanski L, Rauch A, Zweier C, Patkowski D, Laczmanska I: (2010) Study of a Hirschsprung's Disease Patient Cohort Using Multiplex...
    Adv Clin Exp Med. 2010;19(1): 83-88
  • Pasutto F, Reis A: (2010) No Evidence of Association of Heterozygous NTF4 Mutations in Patients with...
    Am J Hum Genet. 2010;86(3): 500-500
  • Isidor B, Pichon O, Redon R, Day-Salvatore D, Hamel A, Siwicka KA, Bitner-Glindzicz M, Heymann D, Kjellén L, Kraus C, Leroy JG, Mortier GR, Rauch A, Verloes A, David A, Le Caignec C: (2010) Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes...
    Am J Hum Genet. 2010;87(1): 95-100
  • Rauen KA, Schoyer L, McCormick F, Lin AE, Allanson JE, Stevenson DA, Gripp KW, Neri G, Carey JC, Legius E, Tartaglia M, Schubbert S, Roberts AE, Gelb BD, Shannon K, Gutmann DH, McMahon M, Guerra C, Fagin JA, Yu B, Aoki Y, Neel BG, Balmain A, Drake RR, Nolan GP, Zenker M, Bollag G, Sebolt-Leopold J, Gibbs JB, Silva AJ, Patton EE, Viskochil DH, Kieran MW, Korf BR, Hagerman RJ, Packer RJ, Melese T: (2010) Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From...
    Am J Med Genet A. 2010;152A(1): 4-24
  • Allanson JE, Bohring A, Dörr HG, Dufke A, Gillessen-Kaesbach G, Horn D, König R, Kratz CP, Kutsche K, Pauli S, Raskin S, Rauch A, Turner A, Wieczorek D, Zenker M: (2010) The face of Noonan syndrome: Does phenotype predict genotype.
    Am J Med Genet A. 2010;152A(8): 1960-6
  • Hüffmeier U, Estivill X, Riveira-Munoz E, Traupe H, Wendler J, Lohmann J, Böhm B, Burkhardt H, Reis A: (2010) Deletion of LCE3C and LCE3B genes at PSORS4 does not contribute to...
    Ann Rheum Dis. 2010;69(5): 876-8
  • Lehmann ML, Selinski S, Blaszkewicz M, Orlich M, Ovsiannikov D, Moormann O, Guballa C, Kress A, Truss MC, Gerullis H, Otto T, Barski D, Niegisch G, Albers P, Frees S, Brenner W, Thüroff JW, Angeli-Greaves M, Seidel T, Roth G, Dietrich H, Ebbinghaus R, Prager HM, Bolt HM, Falkenstein M, Zimmermann A, Klein T, Reckwitz T, Roemer HC, Löhlein D, Weistenhöfer W, Schöps W, Beg AE, Aslam M, Bánfi G, Romics I, Ickstadt K, Schwender H, Winterpacht A, Hengstler JG, Golka K: (2010) Rs710521[A] on chromosome 3q28 close to TP63 is associated with increased...
    Arch Toxicol. 2010;84(12): 967-78
  • Raaz-Schrauder D, Klinghammer L, Ekici AB, Herrmann M, Daniel WG, Reis A, Garlichs CD: (2010) INSTABILITY OF CORONARY PLAQUES IS CLINICALLY AND ANGIOGRAPHICALLY ASSOCIATED...
    Atheroscler Suppl. 2010;11(2): P91 -
  • Raaz-Schrauder D, Ekici AB, Cicha I, Klinghammer L, Herrmann M, Daniel WG, Reis A, Garlichs CD: (2010) ROLE OF FC chi RIIa GENOTYPE FOR THE PROINFLAMMATORY EFFECTS OF C-REACTIVE...
    Atheroscler Suppl. 2010;11(2): W19 -
  • Flotho C, Batz C, Hasle H, Bergsträsser E, van den Heuvel-Eibrink MM, Zecca M, Niemeyer CM, Zenker M: (2010) Mutational analysis of SHOC2, a novel gene for Noonan-like syndrome, in JMML.
    Blood. 2010;115(4): 913
  • Uebe S, Pasutto F, Krumbiegel M, Schanze D, Ekici AB, Reis A: (2010) GPFrontend and GPGraphics: graphical analysis tools for genetic association...
    BMC Bioinformatics. 2010;11: 472
  • Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Wissinger B, Weisschuh N: (2010) Mitochondrial haplogroup U is associated with a reduced risk to develop...
    BMC Genet. 2010;11: 8
  • Choi JS, Cheng X, Foster E, Leffler A, Tyrrell L, Te Morsche RH, Eastman EM, Jansen HJ, Huehne K, Nau C, Dib-Hajj SD, Drenth JP, Waxman SG: (2010) Alternative splicing may contribute to time-dependent manifestation of inherited...
    Brain. 2010;133(Pt 6): 1823-35
  • Milne RL, Gaudet MM, Spurdle AB, Fasching PA, Couch FJ, Benítez J, Arias Pérez JI, Zamora MP, Malats N, Dos Santos Silva I, Gibson LJ, Fletcher O, Johnson N, Anton-Culver H, Ziogas A, Figueroa J, Brinton L, Sherman ME, Lissowska J, Hopper JL, Dite GS, Apicella C, Southey MC, Sigurdson AJ, Linet MS, Schonfeld SJ, Freedman DM, Mannermaa A, Kosma VM, Kataja V, Auvinen P, Andrulis IL, Glendon G, Knight JA, Weerasooriya N, Cox A, Reed MW, Cross SS, Dunning AM, Ahmed S, Shah M, Brauch H, Ko YD, Brüning T, GENICA Network , Lambrechts D, Reumers J, Smeets A, Wang-Gohrke S, Hall P, Czene K, Liu J, Irwanto AK, Chenevix-Trench G, Holland H, kConFab , AOCS , Giles GG, Baglietto L, Severi G, Bojensen SE, Nordestgaard BG, Flyger H, John EM, West DW, Whittemore AS, Vachon C, Olson JE, Fredericksen Z, Kosel M, Hein R, Vrieling A, Flesch-Janys D, Heinz J, Beckmann MW, Heusinger K, Ekici AB, Haeberle L, Humphreys MK, Morrison J, Easton DF, Pharoah PD, García-Closas M, Goode EL, Chang-Claude J: (2010) Assessing interactions between the associations of common genetic susceptibility...
    Breast Cancer Res. 2010;12(6): R110
  • Fletcher O, Johnson N, dos Santos Silva I, Orr N, Ashworth A, Nevanlinna H, Heikkinen T, Aittomäki K, Blomqvist C, Burwinkel B, Bartram CR, Meindl A, Schmutzler RK, Cox A, Brock I, Elliott G, Reed MW, Southey MC, Smith L, Spurdle AB, Hopper JL, Couch FJ, Olson JE, Wang X, Fredericksen Z, Schürmann P, Waltes R, Bremer M, Dörk T, Devilee P, van Asperen CJ, Tollenaar RA, Seynaeve C, Hall P, Czene K, Humphreys K, Liu J, Ahmed S, Dunning AM, Maranian M, Pharoah PD, Chenevix-Trench G, kConFab Investigators , AOCS Group , Beesley J, Bogdanova NV, Antonenkova NN, Zalutsky IV, Anton-Culver H, Ziogas A, Brauch H, Ko YD, Hamann U, GENICA Consortium , Fasching PA, Strick R, Ekici AB, Beckmann MW, Giles GG, Severi G, Baglietto L, English DR, Milne RL, Benítez J, Arias JI, Pita G, Nordestgaard BG, Bojesen SE, Flyger H, Kang D, Yoo KY, Noh DY, Mannermaa A, Kataja V, Kosma VM, García-Closas M, Chanock S, Lissowska J, Brinton LA, Chang-Claude J, Wang-Gohrke S, Broeks A, Schmidt MK, van Leeuwen FE, Van't Veer LJ, Margolin S, Lindblom A, Humphreys MK, Morrison J, Platte R, Easton DF, Peto J, Breast Cancer Association Consortium: (2010) Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls.
    Cancer Epidemiol Biomarkers Prev. 2010;19(9): 2143-51
  • Teupser D, Baber R, Ceglarek U, Scholz M, Illig T, Gieger C, Holdt LM, Leichtle A, Greiser KH, Huster D, Linsel-Nitschke P, Schäfer A, Braund PS, Tiret L, Stark K, Raaz-Schrauder D, Fiedler GM, Wilfert W, Beutner F, Gielen S, Grosshennig A, König IR, Lichtner P, Heid IM, Kluttig A, El Mokhtari NE, Rubin D, Ekici AB, Reis A, Garlichs CD, Hall AS, Matthes G, Wittekind C, Hengstenberg C, Cambien F, Schreiber S, Werdan K, Meitinger T, Loeffler M, Samani NJ, Erdmann J, Wichmann HE, Schunkert H, Thiery J: (2010) Genetic regulation of serum phytosterol levels and risk of coronary artery...
    Circ Cardiovasc Genet. 2010;3(4): 331-9
  • Mkrtchyan H, Gross M, Hinreiner S, Polytiko A, Manvelyan M, Mrasek K, Kosyakova N, Ewers E, Nelle H, Liehr T, Bhatt S, Thoma K, Gebhart E, Wilhelm S, Fahsold R, Volleth M, Weise A: (2010) The human genome puzzle - the role of copy number variation in somatic...
    Curr Genomics. 2010;11(6): 426-31
  • Vulpoi C, Zenker M, Grigoras M, Poeata I, Indrei A, Vasiliu L, Idriceanu J, Mogos V, Rusu C: (2010) Clinical variability of LEOPARD syndrome: Study of a new family
    Endocr J. 2010;57 Suppl. : S620-S620
  • Renard M, Holm T, Veith R, Callewaert BL, Adès LC, Baspinar O, Pickart A, Dasouki M, Hoyer J, Rauch A, Trapane P, Earing MG, Coucke PJ, Sakai LY, Dietz HC, De Paepe AM, Loeys BL: (2010) Altered TGFbeta signaling and cardiovascular manifestations in patients with...
    Eur J Hum Genet. 2010;18(8): 895-901
  • Fabretto A, Kutsche K, Harmsen MB, Demarini S, Gasparini P, Fertz MC, Zenker M: (2010) Two cases of Noonan syndrome with severe respiratory and gastroenteral...
    Eur J Med Genet. 2010;53(5): 322-4
  • Huffmeier U, Traupe H, Mossner R, Reich K, Kurrat W, Estivill X, Riveira-Munoz E, Wendler J, Lohmann J, Bohm B, Burkhardt H, Reis A: (2010) Deletion of LCE3C and LCE3B genes at PSORS4 contributes to susceptibility to...
    Exp Dermatol. 2010;19(2): 178-178
  • Griffin HR, Töpf A, Glen E, Zweier C, Stuart AG, Parsons J, Peart I, Deanfield J, O'Sullivan J, Rauch A, Scambler P, Burn J, Cordell HJ, Keavney B, Goodship JA: (2010) Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot...
    Heart. 2010;96(20): 1651-5
  • Zweier M, Gregor A, Zweier C, Engels H, Sticht H, Wohlleber E, Bijlsma EK, Holder SE, Zenker M, Rossier E, Grasshoff U, Johnson DS, Robertson L, Firth HV, Cornelia Kraus , Ekici AB, Reis A, Rauch A: (2010) Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a...
    Hum Mutat. 2010;31(6): 722-33
  • Dutrannoy V, Demuth I, Baumann U, Schindler D, Konrat K, Neitzel H, Gillessen-Kaesbach G, Radszewski J, Rothe S, Schellenberger MT, Nürnberg G, Nürnberg P, Teik KW, Nallusamy R, Reis A, Sperling K, Digweed M, Varon R: (2010) Clinical variability and novel mutations in the NHEJ1 gene in patients with a...
    Hum Mutat. 2010;31(9): 1059-68
  • Matejas V, Hinkes B, Alkandari F, Al-Gazali L, Annexstad E, Aytac MB, Barrow M, Bláhová K, Bockenhauer D, Cheong HI, Maruniak-Chudek I, Cochat P, Dötsch J, Gajjar P, Hennekam RC, Janssen F, Kagan M, Kariminejad A, Kemper MJ, Koenig J, Kogan J, Kroes HY, Kuwertz-Bröking E, Lewanda AF, Medeira A, Muscheites J, Niaudet P, Pierson M, Saggar A, Seaver L, Suri M, Tsygin A, Wühl E, Zurowska A, Uebe S, Hildebrandt F, Antignac C, Zenker M: (2010) Mutations in the human laminin beta2 (LAMB2) gene and the associated...
    Hum Mutat. 2010;31(9): 992-1002
  • Pasutto F, Chavarria-Soley G, Mardin CY, Michels-Rautenstrauss K, Ingelman-Sundberg M, Fernández-Martínez L, Weber BH, Rautenstrauss B, Reis A: (2010) Heterozygous loss-of-function variants in CYP1B1 predispose to primary...
    Invest Ophthalmol Vis Sci. 2010;51(1): 249-54
  • Smigiel R, Szafranska A, Czyzewska M, Rauch A, Zweier Ch, Patkowski D: (2010) Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome...
    J Appl Genet. 2010;51(1): 111-3
  • Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Gramer G, Wissinger B, Weisschuh N: (2010) Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension...
    J Glaucoma. 2010;19(2): 136-41
  • Krumbiegel M, Pasutto F, Mardin CY, Weisschuh N, Paoli D, Gramer E, Weber BH, Kruse FE, Schlötzer-Schrehardt U, Reis A: (2010) Apolipoprotein E genotypes in pseudoexfoliation syndrome and pseudoexfoliation...
    J Glaucoma. 2010;19(8): 561-5
  • Hüffmeier U, Bergboer JG, Becker T, Armour JA, Traupe H, Estivill X, Riveira-Munoz E, Mössner R, Reich K, Kurrat W, Wienker TF, Schalkwijk J, Zeeuwen PL, Reis A: (2010) Replication of LCE3C-LCE3B CNV as a risk factor for psoriasis and analysis of...
    J Invest Dermatol. 2010;130(4): 979-84
  • Göhring I, Tagariello A, Endele S, Stolt CC, Ghassibé M, Fisher M, Thiel CT, Trautmann U, Vikkula M, Winterpacht A, Fitzpatrick DR, Rauch A: (2010) Disruption of ST5 is associated with mental retardation and multiple...
    J Med Genet. 2010;47(2): 91-8
  • Rauch R, Hofbeck M, Zweier C, Koch A, Zink S, Trautmann U, Hoyer J, Kaulitz R, Singer H, Rauch A: (2010) Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of...
    J Med Genet. 2010;47(5): 321-31
  • Azzato EM, Tyrer J, Fasching PA, Beckmann MW, Ekici AB, Schulz-Wendtland R, Bojesen SE, Nordestgaard BG, Flyger H, Milne RL, Arias JI, Menéndez P, Benítez J, Chang-Claude J, Hein R, Wang-Gohrke S, Nevanlinna H, Heikkinen T, Aittomäki K, Blomqvist C, Margolin S, Mannermaa A, Kosma VM, Kataja V, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer , Beesley J, Chen X, Chenevix-Trench G, Couch FJ, Olson JE, Fredericksen ZS, Wang X, Giles GG, Severi G, Baglietto L, Southey MC, Devilee P, Tollenaar RA, Seynaeve C, García-Closas M, Lissowska J, Sherman ME, Bolton KL, Hall P, Czene K, Cox A, Brock IW, Elliott GC, Reed MW, Greenberg D, Anton-Culver H, Ziogas A, Humphreys M, Easton DF, Caporaso NE, Pharoah PD: (2010) Association between a germline OCA2 polymorphism at chromosome 15q13.1 and...
    J Natl Cancer Inst. 2010;102(9): 650-62
  • Muschler MA, Hillemacher T, Kraus C, Kornhuber J, Bleich S, Frieling H: (2010) DNA methylation of the POMC gene promoter is associated with craving in...
    J Neural Transm. 2010;117(4): 513-9
  • Zweier C, de Jong EK, Oortveld MAW, Zweier M, Reis A, Rauch A, Schenck A: (2010) From human mutations in CNTNAP2/Nrx-IV and NRXN1/Nrx-1 underlying a wide...
    J Neurogenet. 2010;24 1: 13-14
  • Mautner VF, Nguyen R, Bernhard A, von Kodolitsch Y, Zenker M, Kutsche K: (2010) Neuro-cardio-facio-cutaneous syndromes. Overlapping phenotypes with a shared...
    Med. Genet.. 2010;22(1): 10-19
  • Ekici AB, Hilfinger D, Jatzwauk M, Thiel CT, Wenzel D, Lorenz I, Boltshauser E, Goecke TW, Staatz G, Morris-Rosendahl DJ, Sticht H, Hehr U, Reis A, Rauch A: (2010) Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal...
    Mol Syndromol. 2010;1(3): 99-112
  • Cirstea IC, Kutsche K, Dvorsky R, Gremer L, Carta C, Horn D, Roberts AE, Lepri F, Merbitz-Zahradnik T, König R, Kratz CP, Pantaleoni F, Dentici ML, Joshi VA, Kucherlapati RS, Mazzanti L, Mundlos S, Patton MA, Silengo MC, Rossi C, Zampino G, Digilio C, Stuppia L, Seemanova E, Pennacchio LA, Gelb BD, Dallapiccola B, Wittinghofer A, Ahmadian MR, Tartaglia M, Zenker M: (2010) A restricted spectrum of NRAS mutations causes Noonan syndrome.
    Nat Genet. 2010;42(1): 27-9
  • Goode EL, Chenevix-Trench G, Song H, Ramus SJ, Notaridou M, Lawrenson K, Widschwendter M, Vierkant RA, Larson MC, Kjaer SK, Birrer MJ, Berchuck A, Schildkraut J, Tomlinson I, Kiemeney LA, Cook LS, Gronwald J, Garcia-Closas M, Gore ME, Campbell I, Whittemore AS, Sutphen R, Phelan C, Anton-Culver H, Pearce CL, Lambrechts D, Rossing MA, Chang-Claude J, Moysich KB, Goodman MT, Dörk T, Nevanlinna H, Ness RB, Rafnar T, Hogdall C, Hogdall E, Fridley BL, Cunningham JM, Sieh W, McGuire V, Godwin AK, Cramer DW, Hernandez D, Levine D, Lu K, Iversen ES, Palmieri RT, Houlston R, van Altena AM, Aben KK, Massuger LF, Brooks-Wilson A, Kelemen LE, Le ND, Jakubowska A, Lubinski J, Medrek K, Stafford A, Easton DF, Tyrer J, Bolton KL, Harrington P, Eccles D, Chen A, Molina AN, Davila BN, Arango H, Tsai YY, Chen Z, Risch HA, McLaughlin J, Narod SA, Ziogas A, Brewster W, Gentry-Maharaj A, Menon U, Wu AH, Stram DO, Pike MC, Wellcome Trust Case-Control Consortium , Beesley J, Webb PM, Australian Cancer Study (Ovarian Cancer) , Australian Ovarian Cancer Study Group , Ovarian Cancer Association Consortium (OCAC) , Chen X, Ekici AB, Thiel FC, Beckmann MW, Yang H, Wentzensen N, Lissowska J, Fasching PA, Despierre E, Amant F, Vergote I, Doherty J, Hein R, Wang-Gohrke S, Lurie G, Carney ME, Thompson PJ, Runnebaum I, Hillemanns P, Dürst M, Antonenkova N, Bogdanova N, Leminen A, Butzow R, Heikkinen T, Stefansson K, Sulem P, Besenbacher S, Sellers TA, Gayther SA, Pharoah PD, Ovarian Cancer Association Consortium (OCAC): (2010) A genome-wide association study identifies susceptibility loci for ovarian...
    Nat Genet. 2010;42(10): 874-9
  • Bolton KL, Tyrer J, Song H, Ramus SJ, Notaridou M, Jones C, Sher T, Gentry-Maharaj A, Wozniak E, Tsai YY, Weidhaas J, Paik D, Van Den Berg DJ, Stram DO, Pearce CL, Wu AH, Brewster W, Anton-Culver H, Ziogas A, Narod SA, Levine DA, Kaye SB, Brown R, Paul J, Flanagan J, Sieh W, McGuire V, Whittemore AS, Campbell I, Gore ME, Lissowska J, Yang HP, Medrek K, Gronwald J, Lubinski J, Jakubowska A, Le ND, Cook LS, Kelemen LE, Brook-Wilson A, Massuger LF, Kiemeney LA, Aben KK, van Altena AM, Houlston R, Tomlinson I, Palmieri RT, Moorman PG, Schildkraut J, Iversen ES, Phelan C, Vierkant RA, Cunningham JM, Goode EL, Fridley BL, Kruger-Kjaer S, Blaeker J, Hogdall E, Hogdall C, Gross J, Karlan BY, Ness RB, Edwards RP, Odunsi K, Moyisch KB, Baker JA, Modugno F, Heikkinenen T, Butzow R, Nevanlinna H, Leminen A, Bogdanova N, Antonenkova N, Doerk T, Hillemanns P, Dürst M, Runnebaum I, Thompson PJ, Carney ME, Goodman MT, Lurie G, Wang-Gohrke S, Hein R, Chang-Claude J, Rossing MA, Cushing-Haugen KL, Doherty J, Chen C, Rafnar T, Besenbacher S, Sulem P, Stefansson K, Birrer MJ, Terry KL, Hernandez D, Cramer DW, Vergote I, Amant F, Lambrechts D, Despierre E, Fasching PA, Beckmann MW, Thiel FC, Ekici AB, Chen X, Australian Ovarian Cancer Study Group , Australian Cancer Study (Ovarian Cancer) , Ovarian Cancer Association Consortium , Johnatty SE, Webb PM, Beesley J, Chanock S, Garcia-Closas M, Sellers T, Easton DF, Berchuck A, Chenevix-Trench G, Pharoah PD, Gayther SA: (2010) Common variants at 19p13 are associated with susceptibility to ovarian cancer.
    Nat Genet. 2010;42(10): 880-4
  • Endele S, Rosenberger G, Geider K, Popp B, Tamer C, Stefanova I, Milh M, Kortüm F, Fritsch A, Pientka FK, Hellenbroich Y, Kalscheuer VM, Kohlhase J, Moog U, Rappold G, Rauch A, Ropers HH, von Spiczak S, Tönnies H, Villeneuve N, Villard L, Zabel B, Zenker M, Laube B, Reis A, Wieczorek D, Van Maldergem L, Kutsche K: (2010) Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors...
    Nat Genet. 2010;42(11): 1021-6
  • Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2 , Strange A, Capon F, Spencer CC, Knight J, Weale ME, Allen MH, Barton A, Band G, Bellenguez C, Bergboer JG, Blackwell JM, Bramon E, Bumpstead SJ, Casas JP, Cork MJ, Corvin A, Deloukas P, Dilthey A, Duncanson A, Edkins S, Estivill X, Fitzgerald O, Freeman C, Giardina E, Gray E, Hofer A, Hüffmeier U, Hunt SE, Irvine AD, Jankowski J, Kirby B, Langford C, Lascorz J, Leman J, Leslie S, Mallbris L, Markus HS, Mathew CG, McLean WH, McManus R, Mössner R, Moutsianas L, Naluai AT, Nestle FO, Novelli G, Onoufriadis A, Palmer CN, Perricone C, Pirinen M, Plomin R, Potter SC, Pujol RM, Rautanen A, Riveira-Munoz E, Ryan AW, Salmhofer W, Samuelsson L, Sawcer SJ, Schalkwijk J, Smith CH, Ståhle M, Su Z, Tazi-Ahnini R, Traupe H, Viswanathan AC, Warren RB, Weger W, Wolk K, Wood N, Worthington J, Young HS, Zeeuwen PL, Hayday A, Burden AD, Griffiths CE, Kere J, Reis A, McVean G, Evans DM, Brown MA, Barker JN, Peltonen L, Donnelly P, Trembath RC: (2010) A genome-wide association study identifies new psoriasis susceptibility loci and...
    Nat Genet. 2010;42(11): 985-90
  • Hüffmeier U, Uebe S, Ekici AB, Bowes J, Giardina E, Korendowych E, Juneblad K, Apel M, McManus R, Ho P, Bruce IN, Ryan AW, Behrens F, Lascorz J, Böhm B, Traupe H, Lohmann J, Gieger C, Wichmann HE, Herold C, Steffens M, Klareskog L, Wienker TF, Fitzgerald O, Alenius GM, McHugh NJ, Novelli G, Burkhardt H, Barton A, Reis A: (2010) Common variants at TRAF3IP2 are associated with susceptibility to psoriatic...
    Nat Genet. 2010;42(11): 996-9
  • Schoeb DS, Chernin G, Heeringa SF, Matejas V, Held S, Vega-Warner V, Bockenhauer D, Vlangos CN, Moorani KN, Neuhaus TJ, Kari JA, MacDonald J, Saisawat P, Ashraf S, Ovunc B, Zenker M, Hildebrandt F, Gesselschaft für Paediatrische Nephrologie (GPN) Study Group: (2010) Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital...
    Nephrol Dial Transplant. 2010;25(9): 2970-6
  • Huehne K, Schaal U, Leis S, Uebe S, Gosso MF, van den Maagdenberg AM, Maihöfner C, Birklein F, Rautenstrauss B, Winterpacht A: (2010) Lack of genetic association of neutral endopeptidase (NEP) with complex regional...
    Neurosci Lett. 2010;472(1): 19-23
  • Hammer C, Fasching PA, Loehberg CR, Rauh C, Ekici AB, Jud SM, Bani MR, Beckmann MW, Strick R, Niesler B: (2010) Polymorphism in HTR3D shows different risks for acute chemotherapy-induced...
    Pharmacogenomics. 2010;11(7): 943-50
 
 
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