Publikationen 2013
Wissenschaftliche Originalarbeiten
- Ahmad S, Mahmoudi H, Naeem M, Betz RC (2013) Autosomal recessive isolated familial acanthosis nigricans in a Pakistani family due to a homozygous mutation in the insulin receptor gene. British Journal of Dermatology 169:476-478.
- Albayrak
O, Pütter C, Volckmar ALjavascript:setTextFormatInput('strong','insert_form','text_ger','ger');,
Cichon S, Hoffmann P, Nöthen MM, Jöckel KH, Schreiber S, Wichmann HE,
Faraone SV, Neale BM, Herpertz-Dahlmann B, Lehmkuhl G, Sinzig J, Renner
TJ, Romanos M, Warnke A, Lesch KP, Reif A, Schimmelmann BG, Scherag A,
Hebebrand J, Hinney A; Psychiatric GWAS Consortium: ADHD Subgroup (2013)
Common obesity risk alleles in childhood attention-deficit/hyperactivity
disorder. American Journal of Medical Genetics B Neuropsychiatric Genetics
162:295-305.
- Andreassen OA, Djurovic S, Thompson WK, Schork
AJ, Kendler KS, O'Donovan MC, Rujescu D, Werge T, van de Bunt M, Morris
AP, McCarthy MI; International Consortium for Blood Pressure GWAS;
Diabetes Genetics Replication and Meta-analysis Consortium; Psychiatric
Genomics Consortium Schizophrenia Working Group [Cichon S, Nöthen MM],
Roddey JC, McEvoy LK, Desikan RS, Dale AM (2013) Improved detection of
common variants associated with schizophrenia by leveraging pleiotropy
with cardiovascular-disease risk factors. American Journal of Human Genetics 92:197-209.
- Andreassen OA, Thompson WK, Schork AJ, Ripke S,
Mattingsdal M, Kelsoe JR, Kendler KS, O'Donovan MC, Rujescu D, Werge T,
Sklar P; Psychiatric Genomics Consortium (PGC); Bipolar Disorder and
Schizophrenia Working Groups [Cichon S, Degenhardt F, Mühleisen TW, Nöthen
MM, Propping P, Schumacher J], Roddey JC, Chen CH, McEvoy L, Desikan RS,
Djurovic S, Dale AM (2013) Improved detection of common variants
associated with schizophrenia and bipolar disorder using
pleiotropy-informed conditional false discovery rate. PLoS Genetics 9:e1003455.
- Anttila
V, Winsvold BS, Gormley P, Kurth T, Bettella F, McMahon G, Kallela M,
Malik R, de Vries B, Terwindt G, Medland SE, Todt U, McArdle WL, Quaye L,
Koiranen M, Ikram MA, Lehtimäki T, Stam AH, Ligthart L, Wedenoja J, Dunham
I, Neale BM, Palta P, Hamalainen E, Schürks M, Rose LM, Buring JE, Ridker
PM, Steinberg S, Stefansson H, Jakobsson F, Lawlor DA, Evans DM, Ring SM,
Färkkilä M, Artto V, Kaunisto MA, Freilinger T, Schoenen J, Frants RR,
Pelzer N, Weller CM, Zielman R, Heath AC, Madden PA, Montgomery GW, Martin
NG, Borck G, Göbel H, Heinze A, Heinze-Kuhn K, Williams FM, Hartikainen
AL, Pouta A, van den Ende J, Uitterlinden AG, Hofman A, Amin N, Hottenga
JJ, Vink JM, Heikkilä K, Alexander M, Muller-Myhsok B, Schreiber S,
Meitinger T, Wichmann HE, Aromaa A, Eriksson JG, Traynor BJ, Trabzuni D,
Rossin E, Lage K, Jacobs SB, Gibbs JR, Birney E, Kaprio J, Penninx BW,
Boomsma DI, van Duijn C, Raitakari O, Jarvelin MR, Zwart JA, Cherkas L,
Strachan DP, Kubisch C, Ferrari MD, van den Maagdenberg AM, Dichgans M,
Wessman M, Smith GD, Stefansson K, Daly MJ, Nyholt DR, Chasman DI, Palotie
A; North American Brain Expression Consortium; UK Brain Expression
Consortium; International Headache Genetics Consortium (2013) Genome-wide
meta-analysis identifies new susceptibility loci for migraine. Nature
Genetics 45:912-917.
- Aretz S, Genuardi M, Hes FJ (2013) Clinical
utility gene card for: MUTYH-associated polyposis (MAP), autosomal
recessive colorectal adenomatous polyposis, multiple colorectal adenomas,
multiple adenomatous polyps (MAP) - update 2012. European Journal of Human
Genetics 21(1). doi: 10.1038/ejhg.2012.163.
- Baudisch
F*, Draaken M*, Bartels E, Schmiedeke E, Bagci S, Bartmann P, Nöthen MM,
Ludwig M, Reutter H (2013) CNV Analysis in Monozygotic Twin Pairs
Discordant for Urorectal Malformations. Twin
Research and Human Genetics 16:802-807. *These authors contributed equally
to this work.
- Beaty TH, Taub MA, Scott AF, Murray JC, Marazita
ML, Schwender H, Parker MM, Hetmanski JB, Balakrishnan P, Mansilla MA,
Mangold E, Ludwig KU, Noethen MM, Rubini M, Elcioglu N, Ruczinski I (2013)
Confirming genes influencing risk to cleft lip with/without cleft palate
in a case-parent trio study. Human Genetics 132:771-781.
- Berndt
SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE,
Monda KL, Croteau-Chonka DC, Day FR, Esko T, Fall T, Ferreira T, Gentilini
D, Jackson AU, Luan J, Randall JC, Vedantam S, Willer CJ, Winkler TW, Wood
AR, Workalemahu T, Hu YJ, Lee SH, Liang L, Lin DY, Min JL, Neale BM,
Thorleifsson G, Yang J, Albrecht E, Amin N, Bragg-Gresham JL, Cadby G, den
Heijer M, Eklund N, Fischer K, Goel A, Hottenga JJ, Huffman JE, Jarick I,
Johansson Å, Johnson T, Kanoni S, Kleber ME, König IR, Kristiansson K,
Kutalik Z, Lamina C, Lecoeur C, Li G, Mangino M, McArdle WL, Medina-Gomez
C, Müller-Nurasyid M, Ngwa JS, Nolte IM, Paternoster L, Pechlivanis S,
Perola M, Peters MJ, Preuss M, Rose LM, Shi J, Shungin D, Smith AV,
Strawbridge RJ, Surakka I, Teumer A, Trip MD, Tyrer J, Van
Vliet-Ostaptchouk JV, Vandenput L, Waite LL, Zhao JH, Absher D, Asselbergs
FW, Atalay M, Attwood AP, Balmforth AJ, Basart H, Beilby J, Bonnycastle
LL, Brambilla P, Bruinenberg M, Campbell H, Chasman DI, Chines PS, Collins
FS, Connell JM, Cookson WO, de Faire U, de Vegt F, Dei M, Dimitriou M,
Edkins S, Estrada K, Evans DM, Farrall M, Ferrario MM, Ferrières J, Franke
L, Frau F, Gejman PV, Grallert H, Grönberg H, Gudnason V, Hall AS, Hall P,
Hartikainen AL, Hayward C, Heard-Costa NL, Heath AC, Hebebrand J, Homuth
G, Hu FB, Hunt SE, Hyppönen E, Iribarren C, Jacobs KB, Jansson JO, Jula A,
Kähönen M, Kathiresan S, Kee F, Khaw KT, Kivimäki M, Koenig W, Kraja AT,
Kumari M, Kuulasmaa K, Kuusisto J, Laitinen JH, Lakka TA, Langenberg C, Launer
LJ, Lind L, Lindström J, Liu J, Liuzzi A, Lokki ML, Lorentzon M, Madden
PA, Magnusson PK, Manunta P, Marek D, März W, Mateo Leach I, McKnight B,
Medland SE, Mihailov E, Milani L, Montgomery GW, Mooser V, Mühleisen TW,
Munroe PB, Musk AW, Narisu N, Navis G, Nicholson G, Nohr EA, Ong KK,
Oostra BA, Palmer CN, Palotie A, Peden JF, Pedersen N, Peters A, Polasek
O, Pouta A, Pramstaller PP, Prokopenko I, Pütter C, Radhakrishnan A,
Raitakari O, Rendon A, Rivadeneira F, Rudan I, Saaristo TE, Sambrook JG,
Sanders AR, Sanna S, Saramies J, Schipf S, Schreiber S, Schunkert H, Shin
SY, Signorini S, Sinisalo J, Skrobek B, Soranzo N, Stančáková A, Stark K,
Stephens JC, Stirrups K, Stolk RP, Stumvoll M, Swift AJ, Theodoraki EV,
Thorand B, Tregouet DA, Tremoli E, Van der Klauw MM, van Meurs JB,
Vermeulen SH, Viikari J, Virtamo J, Vitart V, Waeber G, Wang Z, Widén E,
Wild SH, Willemsen G, Winkelmann BR, Witteman JC, Wolffenbuttel BH, Wong
A, Wright AF, Zillikens MC, Amouyel P, Boehm BO, Boerwinkle E, Boomsma DI,
Caulfield MJ, Chanock SJ, Cupples LA, Cusi D, Dedoussis GV, Erdmann J,
Eriksson JG, Franks PW, Froguel P, Gieger C, Gyllensten U, Hamsten A,
Harris TB, Hengstenberg C, Hicks AA, Hingorani A, Hinney A, Hofman A,
Hovingh KG, Hveem K, Illig T, Jarvelin MR, Jöckel KH, Keinanen-Kiukaanniemi
SM, Kiemeney LA, Kuh D, Laakso M, Lehtimäki T, Levinson DF, Martin NG,
Metspalu A, Morris AD, Nieminen MS, Njølstad I, Ohlsson C, Oldehinkel AJ,
Ouwehand WH, Palmer LJ, Penninx B, Power C, Province MA, Psaty BM, Qi L,
Rauramaa R, Ridker PM, Ripatti S, Salomaa V, Samani NJ, Snieder H,
Sørensen TI, Spector TD, Stefansson K, Tönjes A, Tuomilehto J,
Uitterlinden AG, Uusitupa M, van der Harst P, Vollenweider P,
Wallaschofski H, Wareham NJ, Watkins H, Wichmann HE, Wilson JF, Abecasis
GR, Assimes TL, Barroso I, Boehnke M, Borecki IB, Deloukas P, Fox CS,
Frayling T, Groop LC, Haritunian T, Heid IM, Hunter D, Kaplan RC, Karpe F,
Moffatt MF, Mohlke KL, O'Connell JR, Pawitan Y, Schadt EE, Schlessinger D,
Steinthorsdottir V, Strachan DP, Thorsteinsdottir U, van Duijn CM,
Visscher PM, Di Blasio AM, Hirschhorn JN, Lindgren CM, Morris AP, Meyre D,
Scherag A, McCarthy MI, Speliotes EK, North KE, Loos RJ, Ingelsson E
(2013) Genome-wide meta-analysis identifies 11 new loci for anthropometric
traits and provides insights into genetic architecture. Nature Genetics
45:501-512.
- Böhmer
AC, Mangold E, Tessmann P, Mossey PA, Steegers-Theunissen RP, Lindemans J,
Bouwman-Both M, Rubini M, Franceschelli P, Aiello V, Peterlin B, Molloy
AM, Nöthen MM, Knapp M, Ludwig KU (2013) Analysis of susceptibility loci
for nonsyndromic orofacial clefting in a European trio sample. American
Journal of Medical Genetics A 161:2545-2549.
- Campeau
PM, Lenk GM, Lu JT, Bae Y, Burrage L, Turnpenny P, Román Corona-Rivera J,
Morandi L, Mora M, Reutter H, Vulto-van Silfhout AT, Faivre L, Haan E,
Gibbs RA, Meisler MH, Lee BH (2013) Yunis-Varón syndrome is caused by
mutations in FIG4, encoding a phosphoinositide phosphatase. American
Journal of Human Genetics 92:781-791.
- Chapman J, Rees E, Harold D, Ivanov D, Gerrish A,
Sims R, Hollingworth P, Stretton A, GERAD1 Consortium [Nöthen MM] ,Holmans
P, Owen MJ, O'Donovan MC, Williams J, Kirov G (2013) A genome-wide study
shows a limited contribution of rare copy number variants to Alzheimer's disease
risk. Human
Molecular Genetics 22:816-824.
- Chen
DT, Jiang X, Akula N, Shugart YY, Wendland JR, Steele CJ, Kassem L, Park
JH, Chatterjee N, Jamain S, Cheng A, Leboyer M, Muglia P, Schulze TG,
Cichon S, Nöthen MM, Rietschel M; BiGS, McMahon FJ, Kelsoe JR, Greenwood
TA, Nievergelt CM, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS,
Nurnberger JI Jr, Edenberg HJ, Foroud T, Koller DL, Gershon ES, Liu C,
Badner JA, Scheftner WA, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice
J, Byerley W, McMahon FJ, Chen DT, Berrettini WH, Potash JB, Zandi PP,
Mahon PB, McInnis MG, Zöllner S, Zhang P, Craig DW, Szelinger S, Barrett
TB, Schulze TG (2013) Genome-wide association study meta-analysis of
European and Asian-ancestry samples identifies three novel loci associated
with bipolar disorder. Molecular Psychiatry 18:195-205.
- Choinitzki
V, Zwink N, Bartels E, Baudisch F, Boemers TM, Hölscher A, Turial S,
Bachour H, Heydweiller A, Kurz R, Bartmann P, Pauly M, Brokmeier U,
Leutner A, Nöthen MM, Schumacher J, Jenetzky E, Reutter H (2013). Second study on the recurrence risk of isolated
esophageal atresia with or without trachea-esophageal fistula among
first-degree relatives: No evidence for increased risk of recurrence of
EA/TEF or for malformations of the VATER/VACTERL association spectrum. Birth Defects Res A Clinical
and Molecular Teratology 97: 786-791.
- Chubb
D, Weinhold N, Broderick P, Chen B, Johnson DC, Försti A, Vijayakrishnan
J, Migliorini G, Dobbins SE, Holroyd A, Hose D, Walker BA, Davies FE, Gregory
WA, Jackson GH, Irving JA, Pratt G, Fegan C, Fenton JA, Neben K, Hoffmann
P, Nöthen MM, Mühleisen TW, Eisele L, Ross FM, Straka C, Einsele H, Langer
C, Dörner E, Allan JM, Jauch A, Morgan GJ, Hemminki K, Houlston RS,
Goldschmidt H (2013) Common variation at 3q26.2, 6p21.33, 17p11.2 and
22q13.1 influences multiple myeloma risk. Nature Genetics 45: 1221-1225.
- Classen CF*, Riehmer V*, Landwehr C, Kosfeld A,
Heilmann S, Scholz C, Kabisch S, Engels H, Tierling S, Zivicnjak M,
Schacherer F, Haffner D**, Weber RG** (2013) Dissecting the genotype in
syndromic intellectual disability using whole exome sequencing in addition
to genome-wide copy number analysis. Human Genetics 132:825-841. *These
authors contributed equally to this work as first authors. **These authors
contributed equally to this work as senior authors.
- Collins AL, Kim Y, Szatkiewicz JP, Bloom RJ,
Hilliard CE, Quackenbush CR, Meier S, Rivas F, Mayoral F, Cichon S, Nöthen
MM, Rietschel M, Sullivan PF (2013) Identifying bipolar disorder susceptibility
loci in a densely affected pedigree. Molecular Psychiatry 18: 1245-1246.
- Cross-Disorder
Group of the Psychiatric Genomics Consortium, Lee SH, Ripke S, Neale BM,
Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte
JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R,
Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA,
Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N,
Battaglia A, Bauer M, Bayés M, Bellivier F, Bergen SE, Berrettini W,
Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH,
Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican
P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM,
Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury
K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin
A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D,
Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S,
Donohoe GJ, Doyle AE, Duan J, Dudbridge F, Duketis E, Ebstein RP, Edenberg
HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger
M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer
NB, Freitag CM, Friedl M, Frisén L, Gallagher L, Gejman PV, Georgieva L,
Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K,
Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan W, Gurling H,
De Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML,
Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S,
Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ,
Hottenga JJ, Hultman CM, Hus V, Ingason A, Ising M, Jamain S, Jones EG,
Jones I, Jones L, Tzeng JY, Kähler AK, Kahn RS, Kandaswamy R, Keller MC,
Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles
JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R,
Kuntsi J, Kwan P, Landén M, Långström N, Lathrop M, Lawrence J, Lawson WB,
Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM,
Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu C, Lohoff FW,
Loo SK, Lord C, Lowe JK, Lucae S, MacIntyre DJ, Madden PA, Maestrini E,
Magnusson PK, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin
NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA,
McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R,
McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE,
Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V,
Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G,
Morris DW, Morrow EM, Moskvina V, Muglia P, Mühleisen TW, Muir WJ,
Müller-Myhsok B, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF,
Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nöthen MM, Nurnberger
JI, Nwulia EA, Nyholt DR, O'Dushlaine C, Oades RD, Olincy A, Oliveira G,
Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato
CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm
J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested
DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Rehnström K,
Reif A, Ribasés M, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L,
Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ,
Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF,
Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG,
Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi J, Shilling PD, Shyn
SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke
EJ, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS,
Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai
S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJ,
Van Grootheest G, Van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher
PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF,
Wijsman EM, Willemsen G, Williams N, Willsey AJ, Witt SH, Xu W, Young AH,
Yu TW, Zammit S, Zandi PP, Zhang P, Zitman FG, Zöllner S; International
Inflammatory Bowel Disease Genetics Consortium (IIBDGC), Devlin B, Kelsoe
JR, Sklar P, Daly MJ, O'Donovan MC, Craddock N, Sullivan PF, Smoller JW,
Kendler KS, Wray NR (2013) Genetic relationship between five psychiatric
disorders estimated from genome-wide SNPs. Nature Genetics 45: 984-994.
- Cross-Disorder Group of the Psychiatric Genomics
Consortium [Cichon S, Degenhardt F, Mühleisen TW, Nöthen MM, Propping P,
Schumacher J], Smoller JW, Craddock N, Kendler K, Lee PH, Neale BM,
Nurnberger JI, Ripke S, Santangelo S, Sullivan PF (2013) Identification of
risk loci with shared effects on five major psychiatric disorders: a
genome-wide analysis. Lancet. 381:1371-1379. Erratum in: Lancet 2013,
381:1360.
- de Blaauw I, Wijers CH, Schmiedeke E,
Holland-Cunz S, Gamba P, Marcelis CL, Reutter H, Aminoff D, Schipper M,
Schwarzer N, Grasshoff-Derr S, Midrio P, Jenetzky E, van Rooij IA (2013)
First results of a European multi-center registry of patients with
anorectal malformations. Journal of Pediatric Surgery 48:2530-2535.
- Defendi F, Charignon D, Ghannam A, Baroso R,
Csopaki F, Allegret-Cadet M, Ponard D, Favier B, Cichon S, Nicolie B, Fain
O, Martin L, Drouet C; National Reference Centre for Angioedema CREAK
(2013) Enzymatic assays for the diagnosis of bradykinin-dependent
angioedema. PLoS
One 8:e70140.
- Degenhardt F*, Priebe L*, Meier S, Lennertz L,
Streit F, Witt SH, Hofmann A, Becker T, Mössner R, Maier W, Nenadic I,
Sauer H, Mattheisen M, Buizer-Voskamp J, Ophoff RA, GROUP Consortium,
Rujescu D, Giegling I, Ingason A, Wagner M, Delobel B, Andrieux J,
Meyer-Lindenberg A, Heinz A, Walter H, Moebus S, Corvin A, Wellcome Trust
Case Control Consortium 2, International Schizophrenia Consortium, deCODE
genetics, Rietschel M, Nöthen MM, Cichon S (2013) Duplications in RB1CC1
are associated with schizophrenia; identification in large European sample
sets. Translational Psychiatr 3:e326. *These authors contributed equally
to this work.
- Degenhardt F, Priebe L, Strohmaier J, Herms S,
Hoffmann P, Mattheisen M, Mössner R, Nenadic I, Sauer H, Rujescu D, Maier
W, Schulze TG, Rietschel M, Nöthen MM, Cichon S (2013) No evidence for an
involvement of copy number variation in ABCA13 in schizophrenia, bipolar
disorder, or major depressive disorder. Psychiatric Genetics 23:45-46.
- Dikow
N, Maas B, Gaspar H, Kreiss-Nachtsheim M, Engels H, Kuechler A, Garbes L,
Netzer C, Neuhann TM, Koehler U, Casteels K, Devriendt K, Janssen JW,
Jauch A, Hinderhofer K, Moog U (2013) The Phenotypic Spectrum Of
Duplication 5q35.2-q35.3 Encompassing NSD1: Is It Really A Reversed Sotos
Syndrome? American Journal of Medical Genetics A 161:2158-2166.
- Draaken
M*, Mughal SS*, Pennimpede T, Wolter S, Wittler L, Ebert AK, Rösch W,
Stein R, Bartels E, Schmidt D, Boemers TM, Schmiedeke E, Hoffmann P,
Moebus S, Herrmann BG, Nöthen MM, Reutter H, Ludwig M (2013) Isolated
bladder exstrophy associated with a de novo 0.9 Mb microduplication on
chromosome 19p13.12. Birth Defects Research A
Clinical Molecular Teratology 97:133-139. *These authors contributed
equally to the work.
- Dworschak GC, Draaken M, Hilger A, Born M,
Reutter H, Ludwig M (2013) An incompletely penetrant novel MAFB
(p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal
osteolysis syndrome. International Journal of Molecular Medicine
32:174-178.
- Dworschak
GC, Draaken M, Marcelis C, de Blaauw I, Pfundt R, van Rooij IA, Bartels E,
Hilger A, Jenetzky E, Schmiedeke E, Grasshoff-Derr S, Schmidt D,
Märzheuser S, Hosie S, Weih S, Holland-Cunz S, Palta M, Leonhardt J,
Schäfer M, Kujath C, Rißmann A, Nöthen MM, Zwink N, Ludwig M, Reutter H
(2013) De novo 13q deletions in two patients with mild anorectal
malformations as part of VATER/VACTERL and VATER/VACTERL-like association
and analysis of EFNB2 in patients with anorectal malformations. American
Journal of Medical Genetics A 161:3035-3041.
- Easton
AC, Lucchesi W, Lourdusamy A, Lenz B, Solati J, Golub Y, Lewczuk P,
Fernandes C, Desrivieres S, Dawirs RR, Moll GH, Kornhuber J, Frank J,
Hoffmann P, Soyka M, Kiefer F; GESGA Consortium [Cichon S, Herms S, Nöthen
MM], Schumann G, Peter Giese K, Müller CP (2013) αCaMKII
autophosphorylation controls the establishment of alcohol drinking
behavior. Neuropsychopharmacology 38:1636-1647. Erratum in:
Neuropsychopharmacology 38:2735.
- Eggermann
T, Elbracht M, Schröder C, Reutter H, Soellner L, Spengler S, Begemann M
(2013) Congenital Imprinting Disorders: A Novel Mechanism Linking
Seemingly Unrelated Disorders. The Journal of Pediatrics 163:1202-1207.
- Ellinghaus
D, Baurecht H, Esparza-Gordillo J, Rodríguez E, Matanovic A, Marenholz I,
Hübner N, Schaarschmidt H, Novak N, Michel S, Maintz L, Werfel T,
Meyer-Hoffert U, Hotze M, Prokisch H, Heim K, Herder C, Hirota T, Tamari
M, Kubo M, Takahashi A, Nakamura Y, Tsoi LC, Stuart P, Elder JT, Sun L,
Zuo X, Yang S, Zhang X, Hoffmann P, Nöthen MM, Fölster-Holst R, Winkelmann
J, Illig T, Boehm BO, Duerr RH, Büning C, Brand S, Glas J, McAleer MA,
Fahy CM, Kabesch M, Brown S, McLean WH, Irvine AD, Schreiber S, Lee YA,
Franke A, Weidinger S (2013) High-density genotyping study identifies four
new susceptibility loci for atopic dermatitis. Nature Genetics 45:808-812.
- Ellinghaus
D, Zhang H, Zeissig S, Lipinski S, Till A, Jiang T, Stade B, Bromberg Y,
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Genetics 21:703-707.
- Fernandes CP, Christoforou A, Giddaluru S,
Ersland KM, Djurovic S, Mattheisen M, Lundervold AJ, Reinvang I, Nöthen
MM, Rietschel M, Ophoff RA; Genetic Risk and Outcome of Psychosis (GROUP),
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Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S,
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Breuer R, Strohmaier J, Degenhardt F, Schmäl C, Lucae S, Maier W,
Rietschel M, Nöthen MM, Cichon S (2013) Genome-wide association data
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L, Tawamie H, Murakami Y, Mang Y, ur Rehman S, Buchert R, Schaffer S,
Muhammad S, Bak M, Nöthen MM, Bennett EP, Maeda Y, Aigner M, Reis A,
Kinoshita T, Tommerup N, Baig SM, Abou Jamra R (2013) Hypomorphic
mutations in PGAP2, encoding a GPI-anchor-remodeling protein, cause
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D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS,
Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan
AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC,
Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D,
McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy
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Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R,
Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE,
Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen
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Walton E, Kirsten H, Liu J, Priebe L, Wolf C, Karbalai N, Gollub R, White
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Association Study Suggests Novel Loci Associated with a
Schizophrenia-Related Brain-Based Phenotype. PLoS One 8:e64872.
- Heilmann S, Brockschmidt FF, Hillmer AM, Hanneken
S, Eigelshoven S, Ludwig KU, Herold C, Mangold E, Becker T, Kruse R, Knapp
M, Nöthen MM (2013) Evidence for a polygenic contribution to androgenetic
alopecia. British
Journal of Dermatology 169:927-930.
- Heilmann S, Kiefer AK, Fricker N, Drichel D,
Hillmer AM, Herold C, Tung JY, Eriksson N, Redler S, Betz RC, Li R,
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NG, Kiemeney LA, Mooser V, Stefansson K, Richards JB, Becker T,
Brockschmidt FF*, Hinds DA*, Nöthen MM* (2013) Androgenetic alopecia:
identification of four genetic risk loci and evidence for the contribution
of WNT signaling to its etiology. Journal of Investigative Dermatology
133:1489-1496. *These authors contributed equally to this work.
- Heilmann S, Nyholt DR, Brockschmidt FF, Hillmer
AM, Herold C; The MAAN consortium, Becker T, Martin NG, Nöthen MM (2013)
No genetic support for a contribution of prostaglandins to the aetiology
of androgenetic alopecia. British Journal of Dermatology 169:222-224.
- Herold C*, Ramirez A*, Drichel D, Lacour A,
Vaitsiakhovich T, Nöthen MM, Jessen F, Maier W, Becker T (2013) A
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One 8:e78038. *These authors contributed equally to this work.
- Hilger A, Schramm C, Pennimpede T, Wittler L,
Dworschak GC, Bartels E, Engels H, Zink AM, Degenhardt F, Müller AM,
Schmiedeke E, Grasshoff-Derr S, Märzheuser S, Hosie S, Holland-Cunz S,
Wijers CH, Marcelis CL, van Rooij IA, Hildebrandt F, Herrmann BG, Nöthen
MM, Ludwig M, Reutter H, Draaken M (2013) De novo microduplications at
1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association. European Journal of Human
Genetics 21:1377-1382.
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benzodiazepines on the adenosine A(2B) receptor mediated secretion of
interleukin-8 in human mast cells. European Journal of Pharmacology 700:152-158.
- Hu YJ, Berndt SI, Gustafsson S, Ganna A; Genetic
Investigation of ANthropometric Traits (GIANT) [Mühleisen TW] Consortium,
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gene-level associations for rare variants based on single-variant
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JT, Seifuddin F, Pirooznia M, Mahon PB; Bipolar Genome Study Consortium,
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Jr, Potash JB, Zandi PP (2013) Converging Evidence for Epistasis between
ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder. Frontiers in
Genetics 2013 May 17;4:87.
- Karagiannidis I, Dehning S, Sandor P, Tarnok Z,
Rizzo R, Wolanczyk T, Madruga-Garrido M, Hebebrand J, Nöthen MM, Lehmkuhl
G, Farkas L, Nagy P, Szymanska U, Anastasiou Z, Stathias V, Androutsos C,
Tsironi V, Koumoula A, Barta C, Zill P, Mir P, Müller N, Barr C, Paschou P
(2013) Support of the histaminergic hypothesis in Tourette Syndrome:
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M, Gockel I, Kaudel P, Gönner U, Kiesslich R, Steinke V, Lang H (2013)
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Figlioli G, Cipollini M, Cristaudo A, Bambi F, Hoffmann P, Herms S,
Kalemba M, Kula D, Harris S, Broderick P, Houlston R, Pastor S, Marcos R,
Velázquez A, Jarzab B, Hemminki K, Landi S, Försti A (2013) Genome-wide
association study on differentiated thyroid cancer. The Journal of Clinical
Endocrinology and Metabolism 98: E1674-1681.
- Krug A, Krach S, Jansen A, Nieratschker V, Witt
SH, Shah NJ, Nöthen MM, Rietschel M, Kircher T (2013) The effect of
neurogranin on neural correlates of episodic memory encoding and
retrieval. Schizophrenia
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- Lambert
JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, Jun G,
Destefano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thornton-Wells
TA, Jones N, Smith AV, Chouraki V, Thomas C, Ikram MA, Zelenika D,
Vardarajan BN, Kamatani Y, Lin CF, Gerrish A, Schmidt H, Kunkle B, Dunstan
ML, Ruiz A, Bihoreau MT, Choi SH, Reitz C, Pasquier F, Hollingworth P,
Ramirez A, Hanon O, Fitzpatrick AL, Buxbaum JD, Campion D, Crane PK,
Baldwin C, Becker T, Gudnason V, Cruchaga C, Craig D, Amin N, Berr C,
Lopez OL, De Jager PL, Deramecourt V, Johnston JA, Evans D, Lovestone S,
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AM, Fiévet N, Huentelman MJ, Gill M, Brown K, Kamboh MI, Keller L,
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Todd S, Wallon D, Love S, Rogaeva E, Gallacher J, St George-Hyslop P,
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Hardy J, Naranjo MC, Bosco P, Clarke R, Brayne C, Galimberti D, Mancuso M,
Matthews F; European Alzheimer's Disease Initiative (EADI); Genetic and
Environmental Risk in Alzheimer's Disease; Alzheimer's Disease Genetic
Consortium; Cohorts for Heart and Aging Research in Genomic Epidemiology,
Moebus S, Mecocci P, Del Zompo M, Maier W, Hampel H, Pilotto A, Bullido M,
Panza F, Caffarra P, Nacmias B, Gilbert JR, Mayhaus M, Lannfelt L,
Hakonarson H, Pichler S, Carrasquillo MM, Ingelsson M, Beekly D, Alvarez
V, Zou F, Valladares O, Younkin SG, Coto E, Hamilton-Nelson KL, Gu W,
Razquin C, Pastor P, Mateo I, Owen MJ, Faber KM, Jonsson PV, Combarros O,
O'Donovan MC, Cantwell LB, Soininen H, Blacker D, Mead S, Mosley TH Jr,
Bennett DA, Harris TB, Fratiglioni L, Holmes C, de Bruijn RF, Passmore P,
Montine TJ, Bettens K, Rotter JI, Brice A, Morgan K, Foroud TM, Kukull WA,
Hannequin D, Powell JF, Nalls MA, Ritchie K, Lunetta KL, Kauwe JS,
Boerwinkle E, Riemenschneider M, Boada M, Hiltunen M, Martin ER, Schmidt
R, Rujescu D, Wang LS, Dartigues JF, Mayeux R, Tzourio C, Hofman A, Nöthen
MM, Graff C, Psaty BM, Jones L, Haines JL, Holmans PA, Lathrop M,
Pericak-Vance MA, Launer LJ, Farrer LA, van Duijn CM, Van Broeckhoven C,
Moskvina V, Seshadri S, Williams J, Schellenberg GD, Amouyel P (2013)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci
for Alzheimer's disease. Nature Genetics 45:1452-1458.
- Lee SH, Harold D, Nyholt DR; ANZGene Consortium;
International Endogene Consortium; Genetic and Environmental Risk for
Alzheimer's disease Consortium [Nöthen MM], Goddard ME, Zondervan KT,
Williams J, Montgomery GW, Wray NR, Visscher PM (2013) Estimation and
partitioning of polygenic variation captured by common SNPs for
Alzheimer's disease, multiple sclerosis and endometriosis. Humen Molecular Genetics
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JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K, Laube
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Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe
P, Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK,
Veri K, Vaher U, Talvik T, Dimova P, Guerrero López R, Serratosa JM,
Linnankivi T, Lehesjoki AE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J,
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Ronen GM, Gruber-Sedlmayr U, Geldner J, Harvey RJ, Hoffmann P, Herms S,
Altmüller J, Toliat MR, Thiele H, Nürnberg P, Wilhelm C, Stephani U,
Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, von Spiczak S
(2013) Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic
spikes. Nature Genetics 45:1067-1072.
- Lencz
T, Guha S, Liu C, Rosenfeld J, Mukherjee S, DeRosse P, John M, Cheng L,
Zhang C, Badner JA, Ikeda M, Iwata N, Cichon S, Rietschel M, Nöthen MM,
Cheng AT, Hodgkinson C, Yuan Q, Kane JM, Lee AT, Pisanté A, Gregersen PK,
Pe'er I, Malhotra AK, Goldman D, Darvasi A (2013) Genome-wide association
study implicates NDST3 in schizophrenia and bipolar disorder. Nature
Communications 4:2739.
- Liu JZ,
Hov JR, Folseraas T, Ellinghaus E, Rushbrook SM, Doncheva NT, Andreassen
OA, Weersma RK, Weismüller TJ, Eksteen B, Invernizzi P, Hirschfield GM,
Gotthardt DN, Pares A, Ellinghaus D, Shah T, Juran BD, Milkiewicz P, Rust
C, Schramm C, Müller T, Srivastava B, Dalekos G, Nöthen MM, Herms S,
Winkelmann J, Mitrovic M, Braun F, Ponsioen CY, Croucher PJ, Sterneck M,
Teufel A, Mason AL, Saarela J, Leppa V, Dorfman R, Alvaro D, Floreani A,
Onengut-Gumuscu S, Rich SS, Thompson WK, Schork AJ, Næss S, Thomsen I,
Mayr G, König IR, Hveem K, Cleynen I, Gutierrez-Achury J, Ricaño-Ponce I,
van Heel D, Björnsson E, Sandford RN, Durie PR, Melum E, Vatn MH,
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Boberg KM, Marschall HU, Chazouillères O, Bowlus CL, Wijmenga C, Schrumpf
E, Vermeire S, Albrecht M; UK-PSCSC Consortium; International IBD Genetics
Consortium, Rioux JD, Alexander G, Bergquist A, Cho J, Schreiber S, Manns
MP, Färkkilä M, Dale AM, Chapman RW, Lazaridis KN; International PSC Study
Group, Franke A, Anderson CA, Karlsen TH (2013) Dense genotyping of
immune-related disease regions identifies nine new risk loci for primary
sclerosing cholangitis. Nature Genetics 45:670-675.
- Lohmann
K, Wilcox RA, Winkler S,
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D, Altenmüller E, Ferbert A, Lang AE, Münchau A, Kostic V, Simonyan K,
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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4
gene. Annals of Neurology 73: 537-545.
- Ludwig
KU, Sämann P, Alexander M, Becker J, Bruder J, Moll K, Spieler D, Czisch
M, Warnke A, Docherty SJ, Davis OS, Plomin R, Nöthen MM, Landerl K,
Müller-Myhsok B, Hoffmann P*, Schumacher J*, Schulte-Körne G*, Czamara D*
(2013) A common variant in Myosin-18B contributes to mathematical
abilities in children with dyslexia and intraparietal sulcus variability
in adults. Translation Psychiatry
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Tazi-Ahnini R, Teßmann P, Giehl KA, Kruse R, Lutz G, Hanneken S, Wolff H,
Blume-Peytavi U, Becker T, Nöthen MM, Messenger AG, Böhm M*, Betz RC*
(2013) Selected variants of the melanocortin 4 receptor gene (MC4R) do not
confer susceptibility to female pattern hair loss. Archives of Dermatological
Research 305:249-253. *These authors contributed equally to this work.
- Major Depressive Disorder Working Group of the
Psychiatric GWAS Consortium [Cichon S, Noethen MM, Degenhardt F, Herms S]
(2013) A mega-analysis of genome-wide association studies for major
depressive disorder. Molecular Psychiatry 18:497-511.
- Manchia
M, Adli M, Akula N, Ardau R, Aubry JM, Backlund L, Banzato CE, Baune BT,
Bellivier F, Bengesser S, Biernacka JM, Brichant-Petitjean C, Bui E,
Calkin CV, Cheng AT, Chillotti C, Cichon S, Clark S, Czerski PM, Dantas C,
Zompo MD, Depaulo JR, Detera-Wadleigh SD, Etain B, Falkai P, Frisén L,
Frye MA, Fullerton J, Gard S, Garnham J, Goes FS, Grof P, Gruber O,
Hashimoto R, Hauser J, Heilbronner U, Hoban R, Hou L, Jamain S, Kahn JP,
Kassem L, Kato T, Kelsoe JR, Kittel-Schneider S, Kliwicki S, Kuo PH,
Kusumi I, Laje G, Lavebratt C, Leboyer M, Leckband SG, López Jaramillo CA,
Maj M, Malafosse A, Martinsson L, Masui T, Mitchell PB, Mondimore F,
Monteleone P, Nallet A, Neuner M, Novák T, O'Donovan C, Osby U, Ozaki N,
Perlis RH, Pfennig A, Potash JB, Reich-Erkelenz D, Reif A, Reininghaus E,
Richardson S, Rouleau GA, Rybakowski JK, Schalling M, Schofield PR,
Schubert OK, Schweizer B, Seemüller F, Grigoroiu-Serbanescu M, Severino G,
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P, Tighe SK, Tortorella A, Turecki G, Wray NR, Wright A, Zandi PP, Zilles
D, Bauer M, Rietschel M, McMahon FJ, Schulze TG, Alda M (2013) Assessment
of Response to Lithium Maintenance Treatment in Bipolar Disorder: A
Consortium on Lithium Genetics (ConLiGen) Report. PLoS One 8:e65636.
- Meier
S, Strohmaier J, Breuer R, Mattheisen M, Degenhardt F, Mühleisen TW,
Schulze TG, Nöthen MM, Cichon S, Rietschel M, Wüst S (2013) Neuregulin 3
is associated with attention deficits in schizophrenia and bipolar
disorder. International Journal of Neuropsychopharmacology 16:549-556.
- Migliorini
G, Fiege B, Hosking FJ, Ma Y, Kumar R, Sherborne AL, da Silva Filho MI,
Vijayakrishnan J, Koehler R, Thomsen H, Irving JA, Allan JM, Lightfoot T,
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E, Kinsey SE, Sheridan E, Thompson P, Hoffmann P, Nöthen MM, Mühleisen TW,
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Hemminki K, Houlston RS (2013) Variation at 10p12.2 and 10p14 influences
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MM, Propping P (2013) Aufklärung genetischer Faktoren bei Volkskrankheiten
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Hanneken S, Wolff H, Böhm M, Becker T, Blume-Peytavi U, Nöthen MM,
Messenger AG, Betz RC (2013) Investigation of six novel susceptibility
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Kaisenberg CS von, Eggermann T, Schwanitz G, Löffler C, Weise A, Mrasek K,
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CG, West H, Harris R, Idziaszczyk S, Maughan TS, Kaplan R, Richman S,
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F, Maier W, Hüll M, Schröder J, Frölich L, Teipel S, Gruber O, Kornhuber
J, Huston JP, Müller CP, Schäble S (2013) Neurokinin3 receptor as a target
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MM, Noori HR, Obermayer K, Rietschel M, Schloss P, Scholz H, Schumann G,
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Addiction GWAS Resource Group, Stringer S, Smits Y, Derks EM (2013) A
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AJ, Thompson WK, Pham P, Torkamani A, Roddey JC, Sullivan PF, Kelsoe JR,
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Psychiatric Genomics Consortium, Schizophrenia Psychiatric Genomics
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Nöthen MM, Propping P, Schumacher J], Schork NJ, Andreassen OA, Dale AM
(2013) All SNPs are not created equal: genome-wide association studies
reveal a consistent pattern of enrichment among functionally annotated
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G, Eggermann T (2013) Nachruf: Prof. Dr. Max Werner Gottschalk.
Medizinische Genetik 2:292.
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SH, Hartz SM, Hoft NR, Saccone NL, Corley RC, Hewitt JK, Hopfer CJ,
Breslau N, Coon H, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Han
Y, Hansel NN, Jiang C, Korhonen T, Lind PA, Liu J, Lyytikäinen LP, Michel
M, Shaffer JR, Short SE, Sun J, Teumer A, Thompson JR, Vogelzangs N, Vink
JM, Wenzlaff A, Wheeler W, Yang BZ, Aggen SH, Balmforth AJ, Baumeister SE,
Beaty TH, Benjamin DJ, Bergen AW, Broms U, Cesarini D, Chatterjee N, Chen
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Giegling I, Gillespie NA, Gu F, Hall AS, Hällfors J, Han S, Hartmann AM,
Heikkilä K, Hickie IB, Hottenga JJ, Jousilahti P, Kaakinen M, Kähönen M,
Koellinger PD, Kittner S, Konte B, Landi MT, Laatikainen T, Leppert M,
Levy SM, Mathias RA, McNeil DW, Medland SE, Montgomery GW, Murray T, Nauck
M, North KE, Paré PD, Pergadia M, Ruczinski I, Salomaa V, Viikari J,
Willemsen G, Barnes KC, Boerwinkle E, Boomsma DI, Caporaso N, Edenberg HJ,
Francks C, Gelernter J, Grabe HJ, Hops H, Jarvelin MR, Johannesson M,
Kendler KS, Lehtimäki T, Magnusson PK, Marazita ML, Marchini J, Mitchell
BD, Nöthen MM, Penninx BW, Raitakari O, Rietschel M, Rujescu D, Samani NJ,
Schwartz AG, Shete S, Spitz M, Swan GE, Völzke H, Veijola J, Wei Q, Amos
C, Cannon DS, Grucza R, Hatsukami D, Heath A, Johnson EO, Kaprio J, Madden
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Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with
onset of regular smoking. Genetic Epidemiology 37:846-859.
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V, Engel C, Büttner R, Schackert HK, Schmiegel WH, Propping P (2013)
Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome.
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V, Propping P, Engel C, Büttner R, Schackert K, Schmiegel WH (2013)
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B, Urbany C, Hoffmann P, Gebhardt C (2013) Population structure and
linkage disequilibrium in dipoid and tetraploid potato revealed by
genome-wide high-density genotyping using the SolCAP SNP array. Plant
Breeding 132:718-724.
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G, Campbell CY, Owens DS, Smith JG, Smith AV, Peloso GM, Kerr KF,
Pechlivanis S, Budoff MJ, Harris TB, Malhotra R, O'Brien KD, Kamstrup PR,
Nordestgaard BG, Tybjaerg-Hansen A, Allison MA, Aspelund T, Criqui MH,
Heckbert SR, Hwang SJ, Liu Y, Sjogren M, van der Pals J, Kälsch H,
Mühleisen TW, Nöthen MM, Cupples LA, Caslake M, Di Angelantonio E, Danesh
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Scheltinga AF Terwisscha, Bakker SC, van Haren NE, Derks EM,
Buizer-Voskamp JE, Boos HB, Cahn W, Hulshoff Pol HE, Ripke S, Ophoff RA,
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jointly modulate total brain and white matter volume. Biological
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Scheltinga AF Terwisscha, Bakker SC, van Haren NE, Derks EM,
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HF, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, Bernstein I,
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Dobbins SE, Hose D, Walker BA, Davies FE, Kaiser MF, Li NL, Gregory WA,
Jackson GH, Witzens-Harig M, Neben K, Hoffmann P, Nöthen MM, Mühleisen TW,
Eisele L, Ross FM, Jauch A, Goldschmidt H, Houlston RS, Morgan GJ, Hemminki
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Y*, Hoffmann P*, Vom Dahl S, Breiden B, Sandhoff R, Niederau C, Horwitz M,
Karlsson S, Filocamo M, Elstein D, Beck M, Sandhoff K, Mengel E, Gonzalez
MC, Nöthen MM, Sidransky E, Zimran A, Mattheisen M (2013) Functional and
genetic characterization of the non-lysosomal glucosylceramidase 2 as a
modifier for Gaucher disease. Orphanet Journal of Rare Diseases 8:151. *These
authors contributed equally to this work.
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Belbin O, Carrasquillo MM, Culley OJ, Hunter TA, Ma L, Bisceglio GD, Allen
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Younkin SG (2013) Linking protective GAB2 variants, increased cortical
GAB2 expression and decreased Alzheimer's disease pathology. PLoS One
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- Zweier
C, Kraus C, Brueton L, Cole T, Degenhardt F, Engels H, Gillessen-Kaesbach
G, Graul-Neumann L, Horn D, Hoyer J, Just W, Rauch A, Reis A, Wollnik B,
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Übersichtsarbeiten / Bücher / Kommentare
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AJ, Degenhardt F, Schratt G, Nöthen MM (2013) MicroRNAs as the cause of
schizophrenia in 22q11.2 deletion carriers, and possible implications for
idiopathic disease: a mini-review. Frontiers in Molecular Neuroscience
6:47.
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P (2013) Die Architektur seelischer Störungen. Frankfurter Allgemeine
Zeitung 13. 11. 2013
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H, Ludwig M (2013) VATER/VACTERL Association: Evidence for the Role of
Genetic Factors. Molecular Syndromology 4:16-19.
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I, Holzapfel S, Steinke V, Aretz S (2013) Genetik gastrointestinaler
Tumoren – Welche Folgen haben Keimbahnmutationen? Gastroenterologe
8:303-3015.