未登录Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function
Lin, Sheng-Jia; Vona, Barbara; Porter, Hillary M.; Izadi, Mahmoud; Huang, Kevin; Lacassie, Yves; Rosenfeld, Jill A.; Khan, Saadullah; Petree, Cassidy; Ali, Tayyiba A.; Muhammad, Nazif; Khan, Sher A.; Muhammad, Noor; Liu, Pengfei; Haymon, Marie-Louise; Rueschendorf, Franz; Kong, Il-Keun; Schnapp, Linda; Shur, Natasha; Chorich, Lynn; Layman, Lawrence; Haaf, Thomas; Pourkarimi, Ehsan; Kim, Hyung-Goo; Varshney, Gaurav K. .png)
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收藏Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4Grosche, Sarah; Marenholz, Ingo; Esparza-Gordillo, Jorge; Arnau-Soler, Aleix; Pairo-Castineira, Erola; Rueschendorf, Franz; Ahluwalia, Tarunveer S.; Almqvist, Catarina; Arnold, Andreas; Baurecht, Hansjoerg; Bisgaard, Hans; Bonnelykke, Klaus; Brown, Sara J.; Bustamante, Mariona; Curtin, John A.; Custovic, Adnan; Dharmage, Shyamali C.; Esplugues, Ana; Falchi, Mario; Fernandez-Orth, Dietmar; Ferreira, Manuel A. R.; Franke, Andre; Gerdes, Sascha; Gieger, Christian; Hakonarson, Hakon; Holt, Patrick G.; Homuth, Georg; Hubner, Norbert; Hysi, Pirro G.; Jarvelin, Marjo-Riitta; Karlsson, Robert; Koppelman, Gerard H.; Lau, Susanne; Lutz, Manuel; Magnusson, Patrik K. E.; Marks, Guy B.; Mueller-Nurasyid, Martina; Noethen, Markus M.; Paternoster, Lavinia; Pennell, Craig E.; Peters, Annette; Rawlik, Konrad; Robertson, Colin F.; Rodriguez, Elke; Sebert, Sylvain; Simpson, Angela; Sleiman, Patrick M. A.; Standl, Marie; Stoelzl, Dora; Strauch, Konstantin; Szwajda, Agnieszka; Tenesa, Albert; Thompson, Philip J.; Ullemar, Vilhelmina; Visconti, Alessia; Vonk, Judith M.; Wang, Carol A.; Weidinger, Stephan; Wielscher, Matthias; Worth, Catherine L.; Xu, Chen-Jian; Lee, Young-Ae 分享 收藏 A biallelic variant in CLRN2 causes non-syndromic hearing loss in humansCLRN2中的双等位基因变体导致人类非综合征性听力损失Vona, Barbara; Mazaheri, Neda; Lin, Sheng-Jia; Dunbar, Lucy A.; Maroofian, Reza; Azaiez, Hela; Booth, Kevin T.; Vitry, Sandrine; Rad, Aboulfazl; Rueschendorf, Franz; Varshney, Pratishtha; Fowler, Ben; Beetz, Christian; Alagramam, Kumar N.; Murphy, David; Shariati, Gholamreza; Sedaghat, Alireza; Houlden, Henry; Petree, Cassidy; VijayKumar, Shruthi; Smith, Richard J. H.; Haaf, Thomas; El-Amraoui, Aziz; Bowl, Michael R.; Varshney, Gaurav K.; Galehdari, Hamid 分享 收藏 Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformationSu, Xiulan; Feng, Yufei; Rahman, Sofia A.; Wu, Shuilong; Li, Guoan; Ruschendorf, Franz; Zhao, Lei; Cui, Hongwei; Liang, Junqing; Fang, Liang; Hu, Hao; Froehler, Sebastian; Yu, Yong; Patone, Giannino; Hummel, Oliver; Chen, Qinghua; Raile, Klemens; Luft, Friedrich C.; Baehring, Sylvia; Hussain, Khalid; Chen, Wei; Zhang, Jingjing; Gong, Maolian 分享 收藏 Age-of-onset information helps identify 76 genetic variants associated with allergic disease发病年龄信息有助于识别与过敏性疾病相关的76种遗传变异Ferreira, Manuel A. R.; Vonk, Judith M.; Baurecht, Hansjoerg; Marenholz, Ingo; Tian, Chao; Hoffman, Joshua D.; Helmer, Quinta; Tillander, Annika; Ullemar, Vilhelmina; Lu, Yi; Grosche, Sarah; Rueschendorf, Franz; Granell, Raquel; Brumpton, Ben M.; Fritsche, Lars G.; Bhatta, Laxmi; Gabrielsen, Maiken E.; Nielsen, Jonas B.; Zhou, Wei; Hveem, Kristian; Langhammer, Arnulf; Holmen, Oddgeir L.; Loset, Mari; Abecasis, Goncalo R.; Willer, Cristen J.; Emami, Nima C.; Cavazos, Taylor B.; Witte, John S.; Szwajda, Agnieszka; Hinds, David A.; Huebner, Norbert; Weidinger, Stephan; Magnusson, Patrik K. E.; Jorgenson, Eric; Karlsson, Robert; Paternoster, Lavinia; Boomsma, Dorret, I; Almqvist, Catarina; Lee, Young-Ae; Koppelman, Gerard H. 分享 收藏 Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autismKim, Hyung-Goo; Rosenfeld, Jill A.; Scott, Daryl A.; Benedicte, Gerard; Labonne, Jonathan D.; Brown, Jason; McGuire, Marianne; Mahida, Sonal; Naidu, Sakkubai; Gutierrez, Jacqueline; Lesca, Gaetan; des Portes, Vincent; Bruel, Ange-Line; Sorlin, Arthur; Xia, Fan; Capri, Yline; Muller, Eric; McKnight, Dianalee; Torti, Erin; Rueschendorf, Franz; Hummel, Oliver; Islam, Zeyaul; Kolatkar, Prasanna R.; Layman, Lawrence C.; Ryu, Duchwan; Kong, Il-Keun; Madan-Khetarpal, Suneeta; Kim, Cheol-Hee 分享 收藏 Eleven loci with new reproducible genetic associations with allergic disease riskFerreira, Manuel A. R.; Vonk, Judith M.; Baurecht, Hansjorg; Marenholz, Ingo; Tian, Chao; Hoffman, Joshua D.; Helmer, Quinta; Tillander, Annika; Ullemar, Vilhelmina; Lu, Yi; Ruschendorf, Franz; Hinds, David A.; Hubner, Norbert; Weidinger, Stephan; Magnusson, Patrik K. E.; Jorgenson, Eric; Lee, Young-Ae; Boomsma, Dorret I.; Karlsson, Robert; Almqvist, Catarina; Koppelman, Gerard H.; Paternoster, Lavinia 分享 收藏 Evaluation of food allergy candidate loci in the Genetics of Food Allergy studyMarenholz, Ingo; Grosche, Sarah; Rueschendorf, Franz; Kalb, Birgit; Blumchen, Katharina; Schlags, Rupert; Harandi, Neda; Price, Mareike; Hansen, Gesine; Seidenberg, Juergen; Yuerek, Songuel; Homuth, Georg; Schmidt, Carsten O.; Noethen, Markus M.; Hubner, Norbert; Niggemann, Bodo; Beyer, Kirsten; Lee, Young-Ae 分享 收藏 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (vol 50, pg 1072, 2018)全基因组关联和HLA精细定位研究确定了过敏性鼻炎的风险位点和遗传途径 (第50卷，1072页，2018)Waage, Johannes; Standl, Marie; Curtin, John A.; Jessen, Leon E.; Thorsen, Jonathan; Tian, Chao; Schoettler, Nathan; Flores, Carlos; Abdellaoui, Abdel; Ahluwalia, Tarunveer S.; Alves, Alexessander C.; Amaral, Andre F. S.; Anto, Josep M.; Arnold, Andreas; Barreto-Luis, Amalia; Baurecht, Hansjorg; van Beijsterveldt, Catharina E. M.; Bleecker, Eugene R.; Bonas-Guarch, Silvia; Boomsma, Dorret I.; Brix, Susanne; Bunyavanich, Supinda; Burchard, Esteban G.; Chen, Zhanghua; Curjuric, Ivan; Custovic, Adnan; den Dekker, Herman T.; Dharmage, Shyamali C.; Dmitrieva, Julia; Duijts, Liesbeth; Ege, Markus J.; Gauderman, W. James; Georges, Michel; Gieger, Christian; Gilliland, Frank; Granell, Raquel; Gui, Hongsheng; Hansen, Torben; Heinrich, Joachim; Henderson, John; Hernandez-Pacheco, Natalia; Holt, Patrick; Imboden, Medea; Jaddoe, Vincent W. V.; Jarvelin, Marjo-Riitta; Jarvis, Deborah L.; Jensen, Kamilla K.; Jonsdottir, Ingileif; Kabesch, Michael; Kaprio, Jaakko; Kumar, Ashish; Lee, Young-Ae; Levin, Albert M.; Li, Xingnan; Lorenzo-Diaz, Fabian; Melen, Erik; Mercader, Josep M.; Meyers, Deborah A.; Myers, Rachel; Nicolae, Dan L.; Nohr, Ellen A.; Palviainen, Teemu; Paternoster, Lavinia; Pennell, Craig E.; Pershagen, Goran; Pino-Yanes, Maria; Probst-Hensch, Nicole M.; Ruschendorf, Franz; Simpson, Angela; Stefansson, Kari; Sunyer, Jordi; Sveinbjornsson, Gardar; Thiering, Elisabeth; Thompson, Philip J.; Torrent, Maties; Torrents, David; Tung, Joyce Y.; Wang, Carol A.; Weidinger, Stephan; Weiss, Scott; Willemsen, Gonneke; Williams, L. Keoki; Ober, Carole; Hinds, David A.; Ferreira, Manuel A.; Bisgaard, Hans; Strachan, David P.; Bonnelykke, Klaus 分享 收藏 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis全基因组关联和HLA精细定位研究确定了变应性鼻炎的风险位点和遗传途径Waage, Johannes; Standl, Marie; Curtin, John A.; Jessen, Leon E.; Thorsen, Jonathan; Tian, Chao; Schoettler, Nathan; Flores, Carlos; Abdellaoui, Abdel; Ahluwalia, Tarunveer S.; Alves, Alexessander C.; Amaral, Andre F. S.; Anto, Josep M.; Arnold, Andreas; Barreto-Luis, Amalia; Baurecht, Hansjoerg; van Beijsterveldt, Catharina E. M.; Bleecker, Eugene R.; Bonas-Guarch, Silvia; Boomsman, Dorret I.; Brix, Susanne; Bunyavanich, Supinda; Burchard, Esteban G.; Chen, Zhanghua; Curjuric, Ivan; Custovic, Adnan; den Dekker, Herman T.; Dharmage, Shyamali C.; Dmitrieva, Julia; Duijts, Liesbeth; Ege, Markus J.; Gauderman, W. James; Georges, Michel; Gieger, Christian; Gilliland, Frank; Granell, Raquel; Gui, Hongsheng; Hansen, Torben; Heinrich, Joachim; Henderson, John; Hernandez-Pacheco, Natalia; Holt, Patrick; Imboden, Medea; Jaddoe, Vincent W. V.; Jarvelin, Marjo-Riitta; Jarvis, Deborah L.; Jensen, Kamilla K.; Jonsdottir, Ingileif; Kabesch, Michael; Kaprio, Jaakko; Kumar, Ashish; Lee, Young-Ae; Levin, Albert M.; Li, Xingnan; Lorenzo-Diaz, Fabian; Melen, Erik; Mercader, Josep M.; Meyers, Deborah A.; Myers, Rachel; Nicolae, Dan L.; Nohr, Ellen A.; Palviainen, Teemu; Paternoster, Lavinia; Pennell, Craig E.; Pershagen, Goran; Pino-Yanes, Maria; Probst-Hensch, Nicole M.; Ruschendorf, Franz; Simpson, Angela; Stefansson, Kari; Sunyer, Jordi; Sveinbjornsson, Gardar; Thiering, Elisabeth; Thompson, Philip J.; Torrent, Maties; Torrents, David; Tung, Joyce Y.; Wang, Carol A.; Weidinger, Stephan; Weiss, Scott; Willemsen, Gonneke; Williams, L. Keoki; Ober, Carole; Hinds, David A.; Ferreira, Manuel A.; Bisgaard, Hans; Strachan, David P.; Bonnelykke, Klaus 分享 收藏 SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer SusceptibilityGuenther, Claudia; Lee-Kirsch, Min Ae; Eckhard, Jamina; Matanovic, Anja; Kerscher, Tamara; Ruschendorf, Franz; Klein, Benjamin; Berndt, Nicole; Zimmermann, Nick; Flachmeier, Christina; Thuss, Theresa; Lucas, Nadja; Marenholz, Ingo; Esparza-Gordillo, Jorge; Huebner, Norbert; Traupe, Heiko; Delaporte, Emmanuel; Lee, Young-Ae 分享 收藏 A Canadian genome-wide association study and meta-analysis confirm HLA as a risk factor for peanut allergy independent of asthmaAsai, Yuka; Eslami, Aida; van Ginkel, C. Dorien; Akhabir, Loubna; Wan, Ming; Yin, David; Ellis, George; Ben-Shoshan, Moshe; Marenholz, Ingo; Martino, David; Ferreira, Manuel A.; Allen, Katrina; Mazer, Bruce; de Groot, Hans; de Jong, Nicolette W.; van Wijk, Roy Gerth; Dubois, Anthony E. J.; Grosche, Sarah; Ashley, Sarah; Rueschendorf, Franz; Kalb, Birgit; Beyer, Kirsten; Noethen, Markus M.; Lee, Young-Ae; Chin, Rick; Cheuk, Stephen; Hoffman, Joshua; Jorgensen, Eric; Witte, John S.; Melles, Ronald B.; Hong, Xiumei; Wang, Xiaobin; Hui, Jennie; Musk, Arthur W. (Bill); Hunter, Michael; James, Alan L.; Koppelman, Gerard H.; Sandford, Andrew J.; Clarke, Ann E.; Daley, Denise 分享 收藏 Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biologyFerreira, Manuel A.; Vonk, Judith M.; Baurecht, Hansjorg; Marenholz, Ingo; Tian, Chao; Hoffman, Joshua D.; Helmer, Quinta; Tillander, Annika; Ullemar, Vilhelmina; van Dongen, Jenny; Lu, Yi; Rueschendorf, Franz; Esparza-Gordillo, Jorge; Medway, Chris W.; Mountjoy, Edward; Burrows, Kimberley; Hummel, Oliver; Grosche, Sarah; Brumpton, Ben M.; Witte, John S.; Hottenga, Jouke-Jan; Willemsen, Gonneke; Zheng, Jie; Rodriguez, Elke; Hotze, Melanie; Franke, Andre; Revez, Joana A.; Beesley, Jonathan; Matheson, Melanie C.; Dharmage, Shyamali C.; Bain, Lisa M.; Fritsche, Lars G.; Gabrielsen, Maiken E.; Balliu, Brunilda; Nielsen, Jonas B.; Zhou, Wei; Hveem, Kristian; Langhammer, Arnulf; Holmen, Oddgeir L.; Loset, Mari; Abecasis, Goncalo R.; Willer, Cristen J.; Arnold, Andreas; Homuth, Georg; Schmidt, Carsten O.; Thompson, Philip J.; Martin, Nicholas G.; Duffy, David L.; Novak, Natalija; Schulz, Holger; Karrasch, Stefan; Gieger, Christian; Strauch, Konstantin; Melles, Ronald B.; Hinds, David A.; Huebner, Norbert; Weidinger, Stephan; Magnusson, Patrik K. E.; Jansen, Rick; Jorgenson, Eric; Lee, Young-Ae; Boomsma, Dorret I.; Almqvist, Catarina; Karlsson, Robert; Koppelman, Gerard H.; Paternoster, Lavinia 分享 收藏 Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergyMarenholz, Ingo; Grosche, Sarah; Kalb, Birgit; Rueschendorf, Franz; Bluemchen, Katharina; Schlags, Rupert; Harandi, Neda; Price, Mareike; Hansen, Gesine; Seidenberg, Juergen; Roeblitz, Holger; Yuerek, Songul; Tschirner, Sebastian; Hong, Xiumei; Wang, Xiaobin; Homuth, Georg; Schmidt, Carsten O.; Noethen, Markus M.; Hubner, Norbert; Niggemann, Bodo; Beyer, Kirsten; Lee, Young-Ae 分享 收藏 Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyHeinig, Matthias; Adriaens, Michiel E.; Schafer, Sebastian; van Deutekom, Hanneke W. M.; Lodder, Elisabeth M.; Ware, James S.; Schneider, Valentin; Felkin, Leanne E.; Creemers, Esther E.; Meder, Benjamin; Katus, Hugo A.; Ruehle, Frank; Stoll, Monika; Cambien, Francois; Villard, Eric; Charron, Philippe; Varro, Andras; Bishopric, Nanette H.; George, Alfred L., Jr.; dos Remedios, Cristobal; Moreno-Moral, Aida; Pesce, Francesco; Bauerfeind, Anja; Rueschendorf, Franz; Rintisch, Carola; Petretto, Enrico; Barton, Paul J.; Cook, Stuart A.; Pinto, Yigal M.; Bezzina, Connie R.; Hubner, Norbert 分享 收藏 Association of TMTC2 With Human Nonsyndromic Sensorineural Hearing LossRunge, Christina L.; Indap, Amit; Zhou, Yifan; Kent, Jack W., Jr.; King, Ericka; Erbe, Christy B.; Cole, Regina; Littrell, Jack; Merath, Kate; James, Roland; Rueschendorf, Franz; Kerschner, Joseph E.; Marth, Gabor; Huebner, Norbert; Goring, Harald H. H.; Friedland, David R.; Kwok, Wai-Meng; Olivier, Michael 分享 收藏 Meta-analysis identifies seven susceptibility loci involved in the atopic marchMarenholz, Ingo; Esparza-Gordillo, Jorge; Rueschendorf, Franz; Bauerfeind, Anja; Strachan, David P.; Spycher, Ben D.; Baurecht, Hansjoerg; Margaritte-Jeannin, Patricia; Saaf, Annika; Kerkhof, Marjan; Ege, Markus; Baltic, Svetlana; Matheson, Melanie C.; Li, Jin; Michel, Sven; Ang, Wei Q.; McArdle, Wendy; Arnold, Andreas; Homuth, Georg; Demenais, Florence; Bouzigon, Emmanuelle; Soderhall, Cilla; Pershagen, Goran; de Jongste, Johan C.; Postma, Dirkje S.; Braun-Fahrlaender, Charlotte; Horak, Elisabeth; Ogorodova, Ludmila M.; Puzyrev, Valery P.; Bragina, Elena Yu; Hudson, Thomas J.; Morin, Charles; Duffy, David L.; Marks, Guy B.; Robertson, Colin F.; Montgomery, Grant W.; Musk, Bill; Thompson, Philip J.; Martin, Nicholas G.; James, Alan; Sleiman, Patrick; Toskala, Elina; Rodriguez, Elke; Foelster-Holst, Regina; Franke, Andre; Lieb, Wolfgang; Gieger, Christian; Heinzmann, Andrea; Rietschel, Ernst; Keil, Thomas; Cichon, Sven; Noethen, Markus M.; Pennell, Craig E.; Sly, Peter D.; Schmidt, Carsten O.; Matanovic, Anja; Schneider, Valentin; Heinig, Matthias; Huebner, Norbert; Holt, Patrick G.; Lau, Susanne; Kabesch, Michael; Weidinger, Stefan; Hakonarson, Hakon; Ferreira, Manuel A. R.; Laprise, Catherine; Freidin, Maxim B.; Genuneit, Jon; Koppelman, Gerard H.; Melen, Erik; Dizier, Marie-Helene; Henderson, A. John; Lee, Young Ae 分享 收藏 Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitisPaternoster, Lavinia; Standl, Marie; Waage, Johannes; Baurecht, Hansjoerg; Hotze, Melanie; Strachan, David P.; Curtin, John A.; Bonnelykke, Klaus; Tian, Chao; Takahashi, Atsushi; Esparza-Gordillo, Jorge; Alves, Alexessander Couto; Thyssen, Jacob P.; den Dekker, Herman T.; Ferreira, Manuel A.; Altmaier, Elisabeth; Sleiman, Patrick M. A.; Xiao, Feng Li; Gonzalez, Juan R.; Marenholz, Ingo; Kalb, Birgit; Pino-Yanes, Maria; Xu, Cheng-Jian; Carstensen, Lisbeth; Groen-Blokhuis, Maria M.; Venturini, Cristina; Pennell, Craig E.; Barton, Sheila J.; Levin, Albert M.; Curjuric, Ivan; Bustamante, Mariona; Kreiner-Moller, Eskil; Lockett, Gabrielle A.; Bacelis, Jonas; Bunyavanich, Supinda; Myers, Rachel A.; Matanovic, Anja; Kumar, Ashish; Tung, Joyce Y.; Hirota, Tomomitsu; Kubo, Michiaki; McArdle, Wendy L.; Henderson, A. John; Kemp, John P.; Zheng, Jie; Smith, George Davey; Rueschendorf, Franz; Bauerfeind, Anja; Lee-Kirsch, Min Ae; Arnold, Andreas; Homuth, Georg; Schmidt, Carsten O.; Mangold, Elisabeth; Cichon, Sven; Keil, Thomas; Rodriguez, Elke; Peters, Annette; Franke, Andre; Lieb, Wolfgang; Novak, Natalija; Foelster-Holst, Regina; Horikoshi, Momoko; Pekkanen, Juha; Sebert, Sylvain; Husemoen, Lise L.; Grarup, Niels; De Jongste, Johan C.; Rivadeneira, Fernando; Hofman, Albert; Jaddoe, Vincent W. V.; Pasmans, Suzanne G. M. A.; Elbert, Niels J.; Uitterlinden, Andre G.; Marks, Guy B.; Thompson, Philip J.; Matheson, Melanie C.; Robertson, Colin F.; Ried, Janina S.; Li, Jin; Zuo, Xian Bo; Zheng, Xiao Dong; Yin, Xian Yong; Sun, Liang Dan; McAleer, Maeve A.; O'Regan, Grainne M.; Fahy, Caoimhe M. R.; Campbell, Linda E.; Macek, Milan; Kurek, Michael; Hu, Donglei; Eng, Celeste; Postma, Dirkje S.; Feenstra, Bjarke; Geller, Frank; Hottenga, Jouke Jan; Middeldorp, Christel M.; Hysi, Pirro; Bataille, Veronique; Spector, Tim; Tiesler, Carla M. T.; Thiering, Elisabeth; Pahukasahasram, Badri; Yang, James J.; Imboden, Medea; Huntsman, Scott; Vilor-Tejedor, Natalia; Relton, Caroline L.; Myhre, Ronny; Nystad, Wenche; Custovic, Adnan; Weiss, Scott T.; Meyers, Deborah A.; Soederhaell, Cilla; Melen, Erik; Ober, Carole; Raby, Benjamin A.; Simpson, Angela; Jacobsson, Bo; Holloway, John W.; Bisgaard, Hans; Sunyer, Jordi; Probst-Hensch, Nicole M.; Williams, L. Keoki; Godfrey, Keith M.; Wang, Carol A.; Boomsma, Dorret I.; Melbye, Mads; Koppelman, Gerard H.; Jarvis, Deborah; McLean, W. H. Irwin; Irvine, Alan D.; Zhang, Xue Jun; Hakonarson, Hakon; Gieger-, Christian; Burchard, Esteban G.; Martin, Nicholas G.; Duijts, Liesbeth; Linneberg, Allan; Jarvelin, Marjo-Riitta; Noethen, Markus M.; Lau, Susanne; Huebner, Norbert; Lee, Young-Ae; Tamari, Mayumi; Hinds, David A.; Glass, Daniel; Brown, Sara J.; Heinrich, Joachim; Evans, David M.; Weidinger, Stephan 分享 收藏 A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitisSchaarschmidt, Heidi; Ellinghaus, David; Rodriguez, Elke; Kretschmer, Anja; Baurecht, Hansjoerg; Lipinski, Simone; Meyer-Hoffert, Ulf; Harder, Juergen; Lieb, Wolfgang; Novak, Natalija; Foelster-Holst, Regina; Esparza-Gordillo, Jorge; Marenholz, Ingo; Ruschendorf, Franz; Hubner, Norbert; Reischl, Eva; Waldenberger, Melanie; Gieger, Christian; Illig, Thomas; Kabesch, Michael; Zhang, Xue-Jun; Xiao, Feng-Li; Lee, Young-Ae; Franke, Andre; Weidinger, Stephan 分享 收藏 PDE3A mutations cause autosomal dominant hypertension with brachydactylyMaass, Philipp G.; Aydin, Atakan; Luft, Friedrich C.; Schaechterle, Carolin; Weise, Anja; Stricker, Sigmar; Lindschau, Carsten; Vaegler, Martin; Qadri, Fatimunnisa; Toka, Hakan R.; Schulz, Herbert; Krawitz, Peter M.; Parkhomchuk, Dmitri; Hecht, Jochen; Hollfinger, Irene; Wefeld-Neuenfeld, Yvette; Bartels-Klein, Eireen; Muehl, Astrid; Kann, Martin; Schuster, Herbert; Chitayat, David; Bialer, Martin G.; Wienker, Thomas F.; Ott, Juerg; Rittscher, Katharina; Liehr, Thomas; Jordan, Jens; Plessis, Ghislaine; Tank, Jens; Mai, Knut; Naraghi, Ramin; Hodge, Russell; Hopp, Maxwell; Hattenbach, Lars O.; Busjahn, Andreas; Rauch, Anita; Vandeput, Fabrice; Gong, Maolian; Rueschendorf, Franz; Huebner, Norbert; Haller, Hermann; Mundlos, Stefan; Bilginturan, Nihat; Movsesian, Matthew A.; Klussmann, Enno; Toka, Okan; Baehring, Sylvia 分享 收藏 
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