2009
Ahting U, Floss T, Uez N, Schneider-Lohmar I, Becker L, Kling E, Iuso A,
Bender A, de Angelis MH, Gailus-Durner V, Fuchs H, Meitinger T, Wurst W, Prokisch
H, Klopstock T. Neurological phenotype and reduced lifespan in heterozygous Tim23
knockout mice, the first mouse model of defective mitochondrial import. Biochim
Biophys Acta. 2009 May;1787(5):371-6. Epub 2008 Dec 9. PubMed PMID: 19111522.
Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, Freimer NB, Jarvelin MR, Gyllensten U, Campbell H, Rudan I, Johansson A, Marroni F, Hayward C, Vitart V, Jonasson I, Pattaro C, Wright A, Hastie N, Pichler I, Hicks AA, Falchi M, Willemsen G, Hottenga JJ, de Geus EJ, Montgomery GW, Whitfield J, Magnusson P, Saharinen J, Perola M, Silander K, Isaacs A, Sijbrands EJ, Uitterlinden AG, Witteman JC, Oostra BA, Elliott P, Ruokonen A, Sabatti C, Gieger C, Meitinger T, Kronenberg F, Döring A, Wichmann HE, Smit JH, McCarthy MI, van Duijn CM, Peltonen L; ENGAGE Consortium. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet. 41(1):47-55 (2009)
Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel
RB, Bis JC, Boerwinkle E, Sinner MF, Dehghan A, Lubitz SA, D'Agostino RB Sr,
Lumley T, Ehret GB, Heeringa J, Aspelund T, Newton-Cheh C, Larson MG, Marciante
KD, Soliman EZ, Rivadeneira F, Wang TJ, Eiríksdottir G, Levy D, Psaty BM, Li M,
Chamberlain AM, Hofman A, Vasan RS, Harris TB, Rotter JI, Kao WH, Agarwal SK,
Stricker BH, Wang K, Launer LJ, Smith NL, Chakravarti A, Uitterlinden AG, Wolf
PA, Sotoodehnia N, Köttgen A, van Duijn CM, Meitinger T, Mueller M, Perz S,
Steinbeck G, Wichmann HE, Lunetta KL, Heckbert SR, Gudnason V, Alonso A, Kääb S,
Ellinor PT, Witteman JC. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat Genet. 2009 Aug;41(8):879-81. Epub 2009 Jul 13. PubMed PMID: 19597492.
Eck S, Benet-Pages A, Flisikowski K, Meitinger T, Fries R, Strom TM. Whole
genome sequencing of a single Bos taurus animal for SNP discovery. Genome Biol.
2009 Aug 6;10(8):R82. [Epub ahead of print] PubMed PMID: 19660108.
Elstner M, Andreoli C, Klopstock T, Meitinger T, Prokisch H. The mitochondrial
proteome database: MitoP2. Methods Enzymol. 2009;457:3-20. PubMed PMID: 19426859.
Enard W, Gehre S, Hammerschmidt K, Hölter SM, Blass T, Somel M, Brückner MK,
Schreiweis C, Winter C, Sohr R, Becker L, Wiebe V, Nickel B, Giger T, Müller U,
Groszer M, Adler T, Aguilar A, Bolle I, Calzada-Wack J, Dalke C, Ehrhardt N,
Favor J, Fuchs H, Gailus-Durner V, Hans W, Hölzlwimmer G, Javaheri A, Kalaydjiev
S, Kallnik M, Kling E, Kunder S, Mossbrugger I, Naton B, Racz I, Rathkolb B,
Rozman J, Schrewe A, Busch DH, Graw J, Ivandic B, Klingenspor M, Klopstock T,
Ollert M, Quintanilla-Martinez L, Schulz H, Wolf E, Wurst W, Zimmer A, Fisher SE,
Morgenstern R, Arendt T, de Angelis MH, Fischer J, Schwarz J, Pääbo S. A
humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell.
2009 May 29;137(5):961-71. PubMed PMID: 19490899.
Erdmann J, Großhennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Trégouët DA, Cambien F, Bruse P, Aherrahrou Z, Wagner AK, Stark K, Schwartz SM, Salomaa V, Elosua R, Melander O, Voight BF, O'Donnell CJ, Peltonen L, Siscovick DS, Altshuler D, Merlini PA, Peyvandi F, Bernardinelli L, Ardissino D, Schillert A, Blankenberg S, Zeller T, Wild P, Schwarz DF, Tiret L, Perret C, Schreiber S, Mokhtari NE, Schäfer A, März W, Renner W, Bugert P, Klüter H, Schrezenmeir J, Rubin D, Ball SG, Balmforth AJ, Wichmann HE, Meitinger T, Fischer M, Meisinger C, Baumert J, Peters A, Ouwehand WH; Italian Atherosclerosis, Thrombosis, and Vascular Biology Working Group; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium; Cardiogenics Consortium, Deloukas P, Thompson JR, Ziegler A, Samani NJ, Schunkert H. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet. 41(3):280-282 (2009)
Favor J, Bradley A, Conte N, Janik D, Pretsch W, Reitmeir P, Rosemann M,
Schmahl W, Wienberg J, Zaus I. Analysis of Pax6 Contiguous Gene Deletions in the
Mouse, Mus musculus, Identifies Regions Distinct from Pax6 Responsible for
Extreme Small Eye and Belly Spotting Phenotypes. Genetics. 2009 May 27. [Epub
ahead of print] PubMed PMID: 19474196.
Fernández-Santiago R, Hoenig S, Lichtner P, Sperfeld AD, Sharma M, Berg D,
Weichenrieder O, Illig T, Eger K, Meyer T, Anneser J, Münch C, Zierz S, Gasser T,
Ludolph A. Identification of novel Angiogenin (ANG) gene missense variants in
German patients with amyotrophic lateral sclerosis. J Neurol. 2009 Apr 12. [Epub
ahead of print] PubMed PMID: 19363631.
Fox AA, Collard CD, Shernan SK, Seidman CE, Seidman JG, Liu KY, Muehlschlegel
JD, Perry TE, Aranki SF, Lange C, Herman DS, Meitinger T, Lichtner P, Body SC.
Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting. Anesthesiology. 110(4):738-47 (2009)
Freilinger T, Bevan S, Ripke S, Gschwendtner A, Lichtner P, Müller-Myhsok B,
Wichmann HE, Markus HS, Meitinger T, Dichgans M. Genetic variation in the
lymphotoxin-alpha pathway and the risk of ischemic stroke in European
populations. Stroke. 2009 Mar;40(3):970-2. Epub 2009 Jan 29. PubMed PMID:
19182073
Fritsche LG, Freitag-Wolf S, Bettecken T, Meitinger T, Keilhauer CN, Krawczak
M, Weber BH. Age-related macular degeneration and functional promoter and coding
variants of the apolipoprotein E gene. Hum Mutat. 2009 Jul;30(7):1048-53. PubMed
PMID: 19384966.
Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wüllner U, Illig T, Sharma M, Gasser T. The transcription factor PITX3 is associated with sporadic Parkinson's disease. Neurobiol Aging. 30(5):731-8 (2009)
Fuchs H, Gailus-Durner V, Adler T, Pimentel JA, Becker L, Bolle I, Brielmeier
M, Calzada-Wack J, Dalke C, Ehrhardt N, Fasnacht N, Ferwagner B, Frischmann U,
Hans W, Hölter SM, Hölzlwimmer G, Horsch M, Javaheri A, Kallnik M, Kling E,
Lengger C, Maier H, Mossbrugger I, Mörth C, Naton B, Nöth U, Pasche B, Prehn C,
Przemeck G, Puk O, Racz I, Rathkolb B, Rozman J, Schäble K, Schreiner R, Schrewe
A, Sina C, Steinkamp R, Thiele F, Willershäuser M, Zeh R, Adamski J, Busch DH,
Beckers J, Behrendt H, Daniel H, Esposito I, Favor J, Graw J, Heldmaier G, Höfler
H, Ivandic B, Katus H, Klingenspor M, Klopstock T, Lengeling A, Mempel M, Müller
W, Neschen S, Ollert M, Quintanilla-Martinez L, Rosenstiel P, Schmidt J,
Schreiber S, Schughart K, Schulz H, Wolf E, Wurst W, Zimmer A, Hrabé de Angelis
M. The German Mouse Clinic: a platform for systemic phenotype analysis of mouse
models. Curr Pharm Biotechnol. 2009 Feb;10(2):236-43. PubMed PMID: 19199957.
Gailus-Durner V, Fuchs H, Adler T, Aguilar Pimentel A, Becker L, Bolle I,
Calzada-Wack J, Dalke C, Ehrhardt N, Ferwagner B, Hans W, Hölter SM, Hölzlwimmer
G, Horsch M, Javaheri A, Kallnik M, Kling E, Lengger C, Mörth C, Mossbrugger I,
Naton B, Prehn C, Puk O, Rathkolb B, Rozman J, Schrewe A, Thiele F, Adamski J,
Aigner B, Behrendt H, Busch DH, Favor J, Graw J, Heldmaier G, Ivandic B, Katus H,
Klingenspor M, Klopstock T, Kremmer E, Ollert M, Quintanilla-Martinez L, Schulz
H, Wolf E, Wurst W, de Angelis MH. Systemic first-line phenotyping. Methods Mol
Biol. 2009;530:463-509. PubMed PMID: 19266331.
Ghezzi D, Goffrini P, Uziel G, Horvath R, Klopstock T, Lochmüller H, D'Adamo
P, Gasparini P, Strom TM, Prokisch H, Invernizzi F, Ferrero I, Zeviani M. SDHAF1,
encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective
infantile leukoencephalopathy. Nat Genet. 2009 May 24. [Epub ahead of print]
PubMed PMID: 19465911.
Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G,
Plazzi G, Nevsimalova S, Bourgin P, Hong SS, Honda Y, Honda M, Högl B, Longstreth
WT Jr, Montplaisir J, Kemlink D, Einen M, Chen J, Musone SL, Akana M, Miyagawa T,
Duan J, Desautels A, Erhardt C, Hesla PE, Poli F, Frauscher B, Jeong JH, Lee SP,
Ton TG, Kvale M, Kolesar L, Dobrovolná M, Nepom GT, Salomon D, Wichmann HE,
Rouleau GA, Gieger C, Levinson DF, Gejman PV, Meitinger T, Young T, Peppard P,
Tokunaga K, Kwok PY, Risch N, Mignot E. Narcolepsy is strongly associated with
the T-cell receptor alpha locus. Nat Genet. 2009 Jun;41(6):708-11. Epub 2009 May
3. PubMed PMID: 19412176.
Hempel M, Rivera Brugués N, Wagenstaller J, Lederer G, Weitensteiner A, Seidel
H, Meitinger T, Strom TM. Microdeletion syndrome 16p11.2-p12.2: Clinical and
molecular characterization. Am J Med Genet A. 2009 Aug 12. [Epub ahead of print]
PubMed PMID: 19676056.
Herlyn H, Zechner U, Oswald F, Pfeufer A, Zischler H, Haaf T. Positive
Selection at Codon 38 of the Human KCNE1 (= minK) Gene and Sporadic Absence of
38Ser-coding mRNAs in Gly38Ser Heterozygotes. BMC Evol Biol. 2009 Aug 6;9(1):188.
[Epub ahead of print] PubMed PMID: 19660109.
Hinterseer M, Beckmann BM, Thomsen MB, Pfeufer A, Dalla Pozza R, Loeff M, Netz
H, Steinbeck G, Vos MA, Kääb S. Relation of increased short-term variability of QT interval to congenital long-QT syndrome. Am J Cardiol. 1;103(9):1244-8 (2009).
Johansson A, Marroni F, Hayward C, Franklin CS, Kirichenko AV, Jonasson I, Hicks AA, Vitart V, Isaacs A, Axenovich T, Campbell S, Dunlop MG, Floyd J, Hastie N, Hofman A, Knott S, Kolcic I, Pichler I, Polasek O, Rivadeneira F, Tenesa A, Uitterlinden AG, Wild SH, Zorkoltseva IV, Meitinger T, Wilson JF, Rudan I, Campbell H, Pattaro C, Pramstaller P, Oostra BA, Wright AF, van Duijn CM, Aulchenko YS, Gyllensten U; EUROSPAN Consortium. Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum Mol Genet. 18(2):373-80 (2009)
Kääb S, Darbar D, van Noord C, Dupuis J, Pfeufer A, Newton-Cheh C, Schnabel R, Makino S, Sinner MF, Kannankeril PJ, Beckmann BM, Choudry S, Donahue BS, Heeringa J, Perz S, Lunetta KL, Larson MG, Levy D, Macrae CA, Ruskin JN, Wacker A, Schömig A, Wichmann HE, Steinbeck G, Meitinger T, Uitterlinden AG, Witteman JC, Roden DM, Benjamin EJ, Ellinor PT. Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur Heart J. 2009 Jan 13. [Epub ahead of print]
Kemlink D, Polo O, Frauscher B, Gschliesser V, Högl B, Poewe W, Vodicka P,
Vavrova J, Sonka K, Nevsimalova S, Schormair B, Lichtner P, Silander K, Peltonen
L, Gieger C, Wichmann HE, Zimprich A, Roeske D, Müller-Myhsok B, Meitinger T,
Winkelmann J. Replication of restless legs syndrome loci in three European
populations. J Med Genet. 2009 May;46(5):315-8. Epub 2009 Mar 10. PubMed PMID:
19279021; PubMed Central PMCID: PMC2695663
Kolz M, Johnson T, Sanna S, Teumer A, Vitart V, Perola M, Mangino M, Albrecht
E, Wallace C, Farrall M, Johansson A, Nyholt DR, Aulchenko Y, Beckmann JS,
Bergmann S, Bochud M, Brown M, Campbell H; EUROSPAN Consortium, Connell J,
Dominiczak A, Homuth G, Lamina C, McCarthy MI; ENGAGE Consortium, Meitinger T,
Mooser V, Munroe P, Nauck M, Peden J, Prokisch H, Salo P, Salomaa V, Samani NJ,
Schlessinger D, Uda M, Völker U, Waeber G, Waterworth D, Wang-Sattler R, Wright
AF, Adamski J, Whitfield JB, Gyllensten U, Wilson JF, Rudan I, Pramstaller P,
Watkins H; PROCARDIS Consortium, Doering A, Wichmann HE; KORA Study, Spector TD, Peltonen L, Völzke H, Nagaraja R, Vollenweider P, Caulfield M; WTCCC, Illig T,
Gieger C. Meta-analysis of 28,141 individuals identifies common variants within
five new loci that influence uric acid concentrations. PLoS Genet. 2009 Jun;5(6):e1000504. Epub 2009 Jun 5. PubMed PMID: 19503597; PubMed Central PMCID: PMC2683940.
Lattka E, Eggers S, Moeller G, Heim K, Weber M, Mehta D, Prokisch H, Illig T, Adamski J. A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1. J Lipid Res. 2009 Jun 22. [Epub ahead of print] PubMed PMID: 19546342.
Linsel-Nitschke P, Heeren J, Aherrahrou Z, Bruse P, Gieger C, Illig T,
Prokisch H, Heim K, Doering A, Peters A, Meitinger T, Wichmann HE, Hinney A,
Reinehr T, Roth C, Ortlepp JR, Soufi M, Sattler AM, Schaefer J, Stark K,
Hengstenberg C, Schaefer A, Schreiber S, Kronenberg F, Samani NJ, Schunkert H,
Erdmann J. Genetic variation at chromosome 1p13.3 affects sortilin mRNA
expression, cellular LDL-uptake and serum LDL levels which translates to the risk
of coronary artery disease. Atherosclerosis. 2009 Jul 8. [Epub ahead of print]
PubMed PMID: 19660754.
Meisinger C, Prokisch H, Gieger C, Soranzo N, Mehta D, Rosskopf D, Lichtner P, Klopp N, Stephens J, Watkins NA, Deloukas P, Greinacher A, Koenig W, Nauck M, Rimmbach C, Völzke H, Peters A, Illig T, Ouwehand WH, Meitinger T, Wichmann HE, Döring A. A genome-wide association study identifies three loci associated with mean platelet volume. Am J Hum Genet. 84(1):66-71 (2009)
Milan DJ, Kim AM, Winterfield JR, Jones IL, Pfeufer A, Sanna S, Arking DE,
Amsterdam AH, Sabeh KM, Mably JD, Rosenbaum DS, Peterson RT, Chakravarti A, Kääb S, Roden DM, MacRae ca. Drug-sensitized zebrafish screen identifies multiple genes, including GINS3, as regulators of myocardial repolarization. Circulation. 2009 Aug 18;120(7):553-9. Epub 2009 Aug 3. PubMed PMID: 19652097.
Mylius V, Gerstner A, Peters M, Prokisch H, Leonhardt A, Hellwig D, Rosenow F. Low-frequency rTMS of the premotor cortex reduces complex movement patterns in a patient with pantothenate kinase-associated neurodegenerative disease (PKAN).
Neurophysiol Clin 39(1):27-30 (2009)
Nelis M, Esko T, Mägi R, Zimprich F, Zimprich A, Toncheva D, Karachanak S,
Piskácková T, Balascák I, Peltonen L, Jakkula E, Rehnström K, Lathrop M, Heath S,
Galan P, Schreiber S, Meitinger T, Pfeufer A, Wichmann HE, Melegh B, Polgár N,
Toniolo D, Gasparini P, D'Adamo P, Klovins J, Nikitina-Zake L, Kucinskas V,
Kasnauskiene J, Lubinski J, Debniak T, Limborska S, Khrunin A, Estivill X,
Rabionet R, Marsal S, Julià A, Antonarakis SE, Deutsch S, Borel C, Attar H,
Gagnebin M, Macek M, Krawczak M, Remm M, Metspalu A. Genetic structure of
Europeans: a view from the North-East. PLoS ONE. 4(5):e5472 (2009)
Newton-Cheh C, Johnson T, Gateva V, Tobin MD, Bochud M, Coin L, Najjar SS,
Zhao JH, Heath SC, Eyheramendy S, Papadakis K, Voight BF, Scott LJ, Zhang F,
Farrall M, Tanaka T, Wallace C, Chambers JC, Khaw KT, Nilsson P, van der Harst P,
Polidoro S, Grobbee DE, Onland-Moret NC, Bots ML, Wain LV, Elliott KS, Teumer A,
Luan J, Lucas G, Kuusisto J, Burton PR, Hadley D, McArdle WL; Wellcome Trust Case
Control Consortium, Brown M, Dominiczak A, Newhouse SJ, Samani NJ, Webster J,
Zeggini E, Beckmann JS, Bergmann S, Lim N, Song K, Vollenweider P, Waeber G,
Waterworth DM, Yuan X, Groop L, Orho-Melander M, Allione A, Di Gregorio A,
Guarrera S, Panico S, Ricceri F, Romanazzi V, Sacerdote C, Vineis P, Barroso I,
Sandhu MS, Luben RN, Crawford GJ, Jousilahti P, Perola M, Boehnke M, Bonnycastle
LL, Collins FS, Jackson AU, Mohlke KL, Stringham HM, Valle TT, Willer CJ, Bergman
RN, Morken MA, Döring A, Gieger C, Illig T, Meitinger T, Org E, Pfeufer A,
Wichmann HE, Kathiresan S, Marrugat J, O'Donnell CJ, Schwartz SM, Siscovick DS,
Subirana I, Freimer NB, Hartikainen AL, McCarthy MI, O'Reilly PF, Peltonen L,
Pouta A, de Jong PE, Snieder H, van Gilst WH, Clarke R, Goel A, Hamsten A, Peden
JF, Seedorf U, Syvänen AC, Tognoni G, Lakatta EG, Sanna S, Scheet P, Schlessinger
D, Scuteri A, Dörr M, Ernst F, Felix SB, Homuth G, Lorbeer R, Reffelmann T,
Rettig R, Völker U, Galan P, Gut IG, Hercberg S, Lathrop GM, Zelenika D, Deloukas
P, Soranzo N, Williams FM, Zhai G, Salomaa V, Laakso M, Elosua R, Forouhi NG,
Völzke H, Uiterwaal CS, van der Schouw YT, Numans ME, Matullo G, Navis G,
Berglund G, Bingham SA, Kooner JS, Connell JM, Bandinelli S, Ferrucci L, Watkins
H, Spector TD, Tuomilehto J, Altshuler D, Strachan DP, Laan M, Meneton P, Wareham
NJ, Uda M, Jarvelin MR, Mooser V, Melander O, Loos RJ, Elliott P, Abecasis GR,
Caulfield M, Munroe PB. Genome-wide association study identifies eight loci
associated with blood pressure. Nat Genet. 2009 May 10. [Epub ahead of print]
Nolte IM, Wallace C, Newhouse SJ, Waggott D, Fu J, Soranzo N, Gwilliam R,
Deloukas P, Savelieva I, Zheng D, Dalageorgou C, Farrall M, Samani NJ, Connell J,
Brown M, Dominiczak A, Lathrop M, Zeggini E, Wain LV; Wellcome Trust Case Control
Consortium; DCCT/EDIC Research Group, Newton-Cheh C, Eijgelsheim M, Rice K, de
Bakker PI; QTGEN consortium, Pfeufer A, Sanna S, Arking DE; QTSCD consortium,
Asselbergs FW, Spector TD, Carter ND, Jeffery S, Tobin M, Caulfield M, Snieder H,
Paterson AD, Munroe PB, Jamshidi Y. Common genetic variation near the
phospholamban gene is associated with cardiac repolarisation: meta-analysis of
three genome-wide association studies. PLoS One. 2009 Jul 9;4(7):e6138. PubMed
PMID: 19587794; PubMed Central PMCID: PMC2704957.
Org E, Eyheramendy S, Juhanson P, Gieger C, Lichtner P, Klopp N, Veldre G,
Döring A, Viigimaa M, Sõber S, Tomberg K, Eckstein G; KORA, Kelgo P, Rebane T,
Shaw-Hawkins S, Howard P, Onipinla A, Dobson RJ, Newhouse SJ, Brown M, Dominiczak A, Connell J, Samani N, Farrall M; BRIGHT, Caulfield MJ, Munroe PB, Illig T, Wichmann HE, Meitinger T, Laan M. Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. Hum Mol Genet. 2009 Jun 15;18(12):2288-96. Epub 2009 Mar 20. PubMed PMID: 19304780; PubMed Central PMCID: PMC2685752.
Parry DA, Toomes C, Bida L, Danciger M, Towns KV, McKibbin M, Jacobson SG,
Logan CV, Ali M, Bond J, Chance R, Swendeman S, Daniele LL, Springell K, Adams M,
Johnson CA, Booth AP, Jafri H, Rashid Y, Banin E, Strom TM, Farber DB, Sharon D,
Blobel CP, Pugh EN Jr, Pierce EA, Inglehearn CF. Loss of the Metalloprotease
ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice. Am J Hum Genet. 2009 Apr 29. [Epub ahead of print]
Petrášek J, Hubáček JA, Stickel F, Sperl J, Berg T, Ruf E, Wichmann HE, Pfeufer A, Meitinger T, Trunečka P, Spičák J, Jirsa M. Do common genetic variants in endotoxin signaling pathway contribute to predisposition to alcoholic liver cirrhosis?
Clin Chem Lab Med. 2009 Mar 12. [Epub ahead of print]
Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, Scuteri A, Prineas RJ, Sinner MF, Gieger C, Najjar SS, Kao WH, Mühleisen TW, Dei M, Happle C, Möhlenkamp S, Crisponi L, Erbel R, Jöckel KH, Naitza S, Steinbeck G, Marroni F, Hicks AA, Lakatta E, Müller-Myhsok B, Pramstaller PP, Wichmann HE, Schlessinger D, Boerwinkle E, Meitinger T, Uda M, Coresh J, Kääb S, Abecasis GR, Chakravarti A. Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat Genet. 41(4):407-14 (2009)
Pretsch W. Triosephosphate isomerase activity-deficient mice show haemolytic
anaemia in homozygous condition. Genet Res. 2009 Feb;91(1):1-4. PubMed PMID:
19220926.
Schlachter K, Gruber-Sedlmayr U, Stogmann E, Lausecker M, Hotzy C, Balzar J, Schuh E, Baumgartner C, Mueller JC, Illig T, Wichmann HE, Lichtner P, Meitinger T, Strom TM, Zimprich A, Zimprich F. A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures. Neurology 72(11):974-8 (2009)
Sinner MF, Pfeufer A, Perz S, Schulze-Bahr E, Mönnig G, Eckardt L, Beckmann
BM, Wichmann HE, Breithardt G, Steinbeck G, Fabritz L, Kääb S, Kirchhof P.
Spontaneous Brugada electrocardiogram patterns are rare in the German general
population: results from the KORA study. Europace. 2009 Aug 4. [Epub ahead of
print] PubMed PMID: 19654127.
Sõber S, Org E, Kepp K, Juhanson P, Eyheramendy S, Gieger C, Lichtner P, Klopp
N, Veldre G, Viigimaa M, Döring A; Kooperative Gesundheitsforschung in der Region
Augsburg Study, Putku M, Kelgo P; HYPertension in ESTonia Study, Shaw-Hawkins S,
Howard P, Onipinla A, Dobson RJ, Newhouse SJ, Brown M, Dominiczak A, Connell J,
Samani N, Farrall M; MRC British Genetics of Hypertension Study, Caulfield MJ,
Munroe PB, Illig T, Wichmann HE, Meitinger T, Laan M. Targeting 160 candidate
genes for blood pressure regulation with a genome-wide genotyping array. PLoS
One. 2009 Jun 29;4(6):e6034. PubMed PMID: 19562039; PubMed Central PMCID:
PMC2699027.
Soranzo N, Rendon A, Gieger C, Jones CI, Watkins NA, Menzel S, Döring A, Stephens J, Prokisch H, Erber W, Potter SC, Bray SL, Burns P, Jolley J, Falchi M, Kühnel B, Erdmann J, Schunkert H, Samani NJ, Illig T, Garner SF, Rankin A, Meisinger C, Bradley JR, Thein SL, Goodall AH, Spector TD, Deloukas P, Ouwehand WH. A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. Blood. 113(16):3831-7 (2009).
Stogmann E, El Tawil S, Wagenstaller J, Gaber A, Edris S, Abdelhady A, Assem-Hilger E, Leutmezer F, Bonelli S, Baumgartner C, Zimprich F, Strom TM, Zimprich A. A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis. Neurogenetics. 10(1):73-7 (2009)
Thiadens AA, den Hollander AI, Roosing S, Nabuurs SB, Zekveld-Vroon RC, Collin
RW, De Baere E, Koenekoop RK, van Schooneveld MJ, Strom TM, van Lith-Verhoeven JJ, Lotery AJ, van Moll-Ramirez N, Leroy BP, van den Born LI, Hoyng CB, Cremers FP, Klaver CC. Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders. Am J Hum Genet. 2009 Aug;85(2):240-7. Epub 2009 Jul 16. PubMed PMID: 1961566
Trégouët DA, König IR, Erdmann J, Munteanu A, Braund PS, Hall AS, Großhennig A, Linsel-Nitschke P, Perret C, Desuremain M, Meitinger T, Wright BJ, Preuss M, Balmforth AJ, Ball SG, Meisinger C, Germain C, Evans A, Arveiler D, Luc G, Ruidavets JB, Morrison C, van der Harst P, Schreiber S, Neureuther K, Schäfer A, Bugert P, El Mokhtari NE, Schrezenmeir J, Stark K, Rubin D, Wichmann HE, Hengstenberg C, Ouwehand W; Wellcome Trust Case Control Consortium; Cardiogenics Consortium, Ziegler A, Tiret L, Thompson JR, Cambien F, Schunkert H, Samani NJ. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet. 41(3):283-285 (2009)
Trenkwalder C, Högl B, Winkelmann J. Recent advances in the diagnosis,
genetics and treatment of restless legs syndrome. J Neurol. 2009
Apr;256(4):539-53. Epub 2009 Apr 27. PubMed PMID: 19444530.
Vasan RS, Glazer NL, Felix JF, Lieb W, Wild PS, Felix SB, Watzinger N, Larson
MG, Smith NL, Dehghan A, Grosshennig A, Schillert A, Teumer A, Schmidt R,
Kathiresan S, Lumley T, Aulchenko YS, König IR, Zeller T, Homuth G, Struchalin M,
Aragam J, Bis JC, Rivadeneira F, Erdmann J, Schnabel RB, Dörr M, Zweiker R, Lind
L, Rodeheffer RJ, Greiser KH, Levy D, Haritunians T, Deckers JW, Stritzke J,
Lackner KJ, Völker U, Ingelsson E, Kullo I, Haerting J, O'Donnell CJ, Heckbert
SR, Stricker BH, Ziegler A, Reffelmann T, Redfield MM, Werdan K, Mitchell GF,
Rice K, Arnett DK, Hofman A, Gottdiener JS, Uitterlinden AG, Meitinger T,
Blettner M, Friedrich N, Wang TJ, Psaty BM, van Duijn CM, Wichmann HE, Munzel TF,
Kroemer HK, Benjamin EJ, Rotter JI, Witteman JC, Schunkert H, Schmidt H, Völzke
H, Blankenberg S. Genetic variants associated with cardiac structure and
function: a meta-analysis and replication of genome-wide association data. JAMA.
2009 Jul 8;302(2):168-78. PubMed PMID: 19584346.
Willer CJ, Speliotes EK, Loos RJ, Li S, Lindgren CM, Heid IM, Berndt SI, Elliott AL, Jackson AU, Lamina C, Lettre G, Lim N, Lyon HN, McCarroll SA, Papadakis K, Qi L, Randall JC, Roccasecca RM, Sanna S, Scheet P, Weedon MN, Wheeler E, Zhao JH, Jacobs LC, Prokopenko I, Soranzo N, Tanaka T, Timpson NJ, Almgren P, Bennett A, Bergman RN, Bingham SA, Bonnycastle LL, Brown M, Burtt NP, Chines P, Coin L, Collins FS, Connell JM, Cooper C, Smith GD, Dennison EM, Deodhar P, Elliott P, Erdos MR, Estrada K, Evans DM, Gianniny L, Gieger C, Gillson CJ, Guiducci C, Hackett R, Hadley D, Hall AS, Havulinna AS, Hebebrand J, Hofman A, Isomaa B, Jacobs KB, Johnson T, Jousilahti P, Jovanovic Z, Khaw KT, Kraft P, Kuokkanen M, Kuusisto J, Laitinen J, Lakatta EG, Luan J, Luben RN, Mangino M, McArdle WL, Meitinger T, Mulas A, Munroe PB, Narisu N, Ness AR, Northstone K, O'Rahilly S, Purmann C, Rees MG, Ridderstråle M, Ring SM, Rivadeneira F, Ruokonen A, Sandhu MS, Saramies J, Scott LJ, Scuteri A, Silander K, Sims MA, Song K, Stephens J, Stevens S, Stringham HM, Tung YC, Valle TT, Van Duijn CM, Vimaleswaran KS, Vollenweider P, Waeber G, Wallace C, Watanabe RM, Waterworth DM, Watkins N; Wellcome Trust Case Control Consortium, Witteman JC, Zeggini E, Zhai G, Zillikens MC, Altshuler D, Caulfield MJ, Chanock SJ, Farooqi IS, Ferrucci L, Guralnik JM, Hattersley AT, Hu FB, Jarvelin MR, Laakso M, Mooser V, Ong KK, Ouwehand WH, Salomaa V, Samani NJ, Spector TD, Tuomi T, Tuomilehto J, Uda M, Uitterlinden AG, Wareham NJ, Deloukas P, Frayling TM, Groop LC, Hayes RB, Hunter DJ, Mohlke KL, Peltonen L, Schlessinger D, Strachan DP, Wichmann HE, McCarthy MI, Boehnke M, Barroso I, Abecasis GR, Hirschhorn JN; Genetic Investigation of ANthropometric Traits Consortium. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet. 41(1):25-34 (2009)
Wjst M, Lichtner P, Meitinger T, Grimbacher B. STAT3 single-nucleotide polymorphisms and STAT3 mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families. Eur J Hum Genet. 17(3):352-6 (2009)
Zimprich A, Schulte C, Reinthaler E, Haubenberger D, Balzar J, Lichtner P, El
Tawil S, Edris S, Foki T, Pirker W, Katzenschlager R, Daniel G, Brücke T, Auff E,
Gasser T. PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease. Parkinsonism Relat Disord. 2009 Aug;15(7):532-4. Epub 2009 Feb 27. PubMed PMID: 19250854.