Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.
Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Implementation of a Renal Precision Medicine Program: Clinician Attitudes and Acceptance.
Life (Basel, Switzerland)
Spiech, Katherine M KM; Tripathy, Purnima R PR; Woodcock, Alex M AM; Sheth, Nehal A NA; Collins, Kimberly S KS; Kannegolla, Karthik K; Sinha, Arjun D AD; Sharfuddin, Asif A AA; Pratt, Victoria M VM; Khalid, Myda M; Hains, David S DS; Moe, Sharon M SM; Skaar, Todd C TC; Moorthi, Ranjani N RN; Eadon, Michael T MT
Genetic Susceptibility to Chronic Kidney Disease - Some More Pieces for the Heritability Puzzle.
Frontiers In Genetics
Cañadas-Garre, Marisa M; Anderson, Kerry K; Cappa, Ruaidhri R; Skelly, Ryan R; Smyth, Laura Jane LJ; McKnight, Amy Jayne AJ; Maxwell, Alexander Peter AP
Clinical and genetic associations of renal function and diabetic kidney disease in the United Arab Emirates: a cross-sectional study.
Bmj Open
Osman, Wael M WM; Jelinek, Herbert F HF; Tay, Guan K GK; Khandoker, Ahsan H AH; Khalaf, Kinda K; Almahmeed, Wael W; Hassan, Mohamed H MH; Alsafar, Habiba S HS
Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy.
Pharmacogenetics And Genomics
Collins, Kimberly S KS; Pratt, Victoria M VM; Stansberry, Wesley M WM; Medeiros, Elizabeth B EB; Kannegolla, Karthik K; Swart, Marelize M; Skaar, Todd C TC; Chapman, Arlene B AB; Decker, Brian S BS; Moorthi, Ranjani N RN; Eadon, Michael T MT
Publication Date: 2019-01
Variant appearance in text: SHROOM3: 168+11474G>A; rs17319721
Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.
Journal Of The American Society Of Nephrology : Jasn
Prokop, Jeremy W JW; Yeo, Nan Cher NC; Ottmann, Christian C; Chhetri, Surya B SB; Florus, Kacie L KL; Ross, Emily J EJ; Sosonkina, Nadiya N; Link, Brian A BA; Freedman, Barry I BI; Coppola, Candice J CJ; McDermott-Roe, Chris C; Leysen, Seppe S; Milroy, Lech-Gustav LG; Meijer, Femke A FA; Geurts, Aron M AM; Rauscher, Frank J FJ; Ramaker, Ryne R; Flister, Michael J MJ; Jacob, Howard J HJ; Mendenhall, Eric M EM; Lazar, Jozef J
Association between kidney function and genetic polymorphisms in atherosclerotic and chronic kidney diseases: A cross-sectional study in Japanese male workers.
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
Scientific Reports
Gorski, Mathias M; van der Most, Peter J PJ; Teumer, Alexander A; Chu, Audrey Y AY; Li, Man M; Mijatovic, Vladan V; Nolte, Ilja M IM; Cocca, Massimiliano M; Taliun, Daniel D; Gomez, Felicia F; Li, Yong Y; Tayo, Bamidele B; Tin, Adrienne A; Feitosa, Mary F MF; Aspelund, Thor T; Attia, John J; Biffar, Reiner R; Bochud, Murielle M; Boerwinkle, Eric E; Borecki, Ingrid I; Bottinger, Erwin P EP; Chen, Ming-Huei MH; Chouraki, Vincent V; Ciullo, Marina M; Coresh, Josef J; Cornelis, Marilyn C MC; Curhan, Gary C GC; d'Adamo, Adamo Pio AP; Dehghan, Abbas A; Dengler, Laura L; Ding, Jingzhong J; Eiriksdottir, Gudny G; Endlich, Karlhans K; Enroth, Stefan S; Esko, Tõnu T; Franco, Oscar H OH; Gasparini, Paolo P; Gieger, Christian C; Girotto, Giorgia G; Gottesman, Omri O; Gudnason, Vilmundur V; Gyllensten, Ulf U; Hancock, Stephen J SJ; Harris, Tamara B TB; Helmer, Catherine C; Höllerer, Simon S; Hofer, Edith E; Hofman, Albert A; Holliday, Elizabeth G EG; Homuth, Georg G; Hu, Frank B FB; Huth, Cornelia C; Hutri-Kähönen, Nina N; Hwang, Shih-Jen SJ; Imboden, Medea M; Johansson, Åsa Å; Kähönen, Mika M; König, Wolfgang W; Kramer, Holly H; Krämer, Bernhard K BK; Kumar, Ashish A; Kutalik, Zoltan Z; Lambert, Jean-Charles JC; Launer, Lenore J LJ; Lehtimäki, Terho T; de Borst, Martin M; Navis, Gerjan G; Swertz, Morris M; Liu, Yongmei Y; Lohman, Kurt K; Loos, Ruth J F RJF; Lu, Yingchang Y; Lyytikäinen, Leo-Pekka LP; McEvoy, Mark A MA; Meisinger, Christa C; Meitinger, Thomas T; Metspalu, Andres A; Metzger, Marie M; Mihailov, Evelin E; Mitchell, Paul P; Nauck, Matthias M; Oldehinkel, Albertine J AJ; Olden, Matthias M; Wjh Penninx, Brenda B; Pistis, Giorgio G; Pramstaller, Peter P PP; Probst-Hensch, Nicole N; Raitakari, Olli T OT; Rettig, Rainer R; Ridker, Paul M PM; Rivadeneira, Fernando F; Robino, Antonietta A; Rosas, Sylvia E SE; Ruderfer, Douglas D; Ruggiero, Daniela D; Saba, Yasaman Y; Sala, Cinzia C; Schmidt, Helena H; Schmidt, Reinhold R; Scott, Rodney J RJ; Sedaghat, Sanaz S; Smith, Albert V AV; Sorice, Rossella R; Stengel, Benedicte B; Stracke, Sylvia S; Strauch, Konstantin K; Toniolo, Daniela D; Uitterlinden, Andre G AG; Ulivi, Sheila S; Viikari, Jorma S JS; Völker, Uwe U; Vollenweider, Peter P; Völzke, Henry H; Vuckovic, Dragana D; Waldenberger, Melanie M; Jin Wang, Jie J; Yang, Qiong Q; Chasman, Daniel I DI; Tromp, Gerard G; Snieder, Harold H; Heid, Iris M IM; Fox, Caroline S CS; Köttgen, Anna A; Pattaro, Cristian C; Böger, Carsten A CA; Fuchsberger, Christian C
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
Nature Genetics
Iotchkova, Valentina V; Huang, Jie J; Morris, John A JA; Jain, Deepti D; Barbieri, Caterina C; Walter, Klaudia K; Min, Josine L JL; Chen, Lu L; Astle, William W; Cocca, Massimilian M; Deelen, Patrick P; Elding, Heather H; Farmaki, Aliki-Eleni AE; Franklin, Christopher S CS; Franberg, Mattias M; Gaunt, Tom R TR; Hofman, Albert A; Jiang, Tao T; Kleber, Marcus E ME; Lachance, Genevieve G; Luan, Jian'an J; Malerba, Giovanni G; Matchan, Angela A; Mead, Daniel D; Memari, Yasin Y; Ntalla, Ioanna I; Panoutsopoulou, Kalliope K; Pazoki, Raha R; Perry, John R B JRB; Rivadeneira, Fernando F; Sabater-Lleal, Maria M; Sennblad, Bengt B; Shin, So-Youn SY; Southam, Lorraine L; Traglia, Michela M; van Dijk, Freerk F; van Leeuwen, Elisabeth M EM; Zaza, Gianluigi G; Zhang, Weihua W; , ; Amin, Najaf N; Butterworth, Adam A; Chambers, John C JC; Dedoussis, George G; Dehghan, Abbas A; Franco, Oscar H OH; Franke, Lude L; Frontini, Mattia M; Gambaro, Giovanni G; Gasparini, Paolo P; Hamsten, Anders A; Issacs, Aaron A; Kooner, Jaspal S JS; Kooperberg, Charles C; Langenberg, Claudia C; Marz, Winfried W; Scott, Robert A RA; Swertz, Morris A MA; Toniolo, Daniela D; Uitterlinden, Andre G AG; van Duijn, Cornelia M CM; Watkins, Hugh H; Zeggini, Eleftheria E; Maurano, Mathew T MT; Timpson, Nicholas J NJ; Reiner, Alexander P AP; Auer, Paul L PL; Soranzo, Nicole N
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
Human Molecular Genetics
Lamina, Claudia C; Friedel, Salome S; Coassin, Stefan S; Rueedi, Rico R; Yousri, Noha A NA; Seppälä, Ilkka I; Gieger, Christian C; Schönherr, Sebastian S; Forer, Lukas L; Erhart, Gertraud G; Kollerits, Barbara B; Marques-Vidal, Pedro P; Ried, Janina J; Waeber, Gerard G; Bergmann, Sven S; Dähnhardt, Doreen D; Stöckl, Andrea A; Kiechl, Stefan S; Raitakari, Olli T OT; Kähönen, Mika M; Willeit, Johann J; Kedenko, Ludmilla L; Paulweber, Bernhard B; Peters, Annette A; Meitinger, Thomas T; Strauch, Konstantin K; , ; Lehtimäki, Terho T; Hunt, Steven C SC; Vollenweider, Peter P; Kronenberg, Florian F
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Nature Communications
Pattaro, Cristian C; Teumer, Alexander A; Gorski, Mathias M; Chu, Audrey Y AY; Li, Man M; Mijatovic, Vladan V; Garnaas, Maija M; Tin, Adrienne A; Sorice, Rossella R; Li, Yong Y; Taliun, Daniel D; Olden, Matthias M; Foster, Meredith M; Yang, Qiong Q; Chen, Ming-Huei MH; Pers, Tune H TH; Johnson, Andrew D AD; Ko, Yi-An YA; Fuchsberger, Christian C; Tayo, Bamidele B; Nalls, Michael M; Feitosa, Mary F MF; Isaacs, Aaron A; Dehghan, Abbas A; d'Adamo, Pio P; Adeyemo, Adebowale A; Dieffenbach, Aida Karina AK; Zonderman, Alan B AB; Nolte, Ilja M IM; van der Most, Peter J PJ; Wright, Alan F AF; Shuldiner, Alan R AR; Morrison, Alanna C AC; Hofman, Albert A; Smith, Albert V AV; Dreisbach, Albert W AW; Franke, Andre A; Uitterlinden, Andre G AG; Metspalu, Andres A; Tonjes, Anke A; Lupo, Antonio A; Robino, Antonietta A; Johansson, Åsa Å; Demirkan, Ayse A; Kollerits, Barbara B; Freedman, Barry I BI; Ponte, Belen B; Oostra, Ben A BA; Paulweber, Bernhard B; Krämer, Bernhard K BK; Mitchell, Braxton D BD; Buckley, Brendan M BM; Peralta, Carmen A CA; Hayward, Caroline C; Helmer, Catherine C; Rotimi, Charles N CN; Shaffer, Christian M CM; Müller, Christian C; Sala, Cinzia C; van Duijn, Cornelia M CM; Saint-Pierre, Aude A; Ackermann, Daniel D; Shriner, Daniel D; Ruggiero, Daniela D; Toniolo, Daniela D; Lu, Yingchang Y; Cusi, Daniele D; Czamara, Darina D; Ellinghaus, David D; Siscovick, David S DS; Ruderfer, Douglas D; Gieger, Christian C; Grallert, Harald H; Rochtchina, Elena E; Atkinson, Elizabeth J EJ; Holliday, Elizabeth G EG; Boerwinkle, Eric E; Salvi, Erika E; Bottinger, Erwin P EP; Murgia, Federico F; Rivadeneira, Fernando F; Ernst, Florian F; Kronenberg, Florian F; Hu, Frank B FB; Navis, Gerjan J GJ; Curhan, Gary C GC; Ehret, George B GB; Homuth, Georg G; Coassin, Stefan S; Thun, Gian-Andri GA; Pistis, Giorgio G; Gambaro, Giovanni G; Malerba, Giovanni G; Montgomery, Grant W GW; Eiriksdottir, Gudny G; Jacobs, Gunnar G; Li, Guo G; Wichmann, H-Erich HE; Campbell, Harry H; Schmidt, Helena H; 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Haun, Margot M; Cornelis, Marilyn C MC; Ciullo, Marina M; Pirastu, Mario M; de Andrade, Mariza M; McEvoy, Mark A MA; Woodward, Mark M; Adam, Martin M; Cocca, Massimiliano M; Nauck, Matthias M; Imboden, Medea M; Waldenberger, Melanie M; Pruijm, Menno M; Metzger, Marie M; Stumvoll, Michael M; Evans, Michele K MK; Sale, Michele M MM; Kähönen, Mika M; Boban, Mladen M; Bochud, Murielle M; Rheinberger, Myriam M; Verweij, Niek N; Bouatia-Naji, Nabila N; Martin, Nicholas G NG; Hastie, Nick N; Probst-Hensch, Nicole N; Soranzo, Nicole N; Devuyst, Olivier O; Raitakari, Olli O; Gottesman, Omri O; Franco, Oscar H OH; Polasek, Ozren O; Gasparini, Paolo P; Munroe, Patricia B PB; Ridker, Paul M PM; Mitchell, Paul P; Muntner, Paul P; Meisinger, Christa C; Smit, Johannes H JH; , ; , ; , ; , ; , ; Kovacs, Peter P; Wild, Philipp S PS; Froguel, Philippe P; Rettig, Rainer R; Mägi, Reedik R; Biffar, Reiner R; Schmidt, Reinhold R; Middelberg, Rita P S RP; Carroll, Robert J RJ; Penninx, Brenda W BW; Scott, Rodney J RJ; Katz, Ronit R; Sedaghat, Sanaz S; Wild, Sarah H SH; Kardia, Sharon L R SL; Ulivi, Sheila S; Hwang, Shih-Jen SJ; Enroth, Stefan S; Kloiber, Stefan S; Trompet, Stella S; Stengel, Benedicte B; Hancock, Stephen J SJ; Turner, Stephen T ST; Rosas, Sylvia E SE; Stracke, Sylvia S; Harris, Tamara B TB; Zeller, Tanja T; Zemunik, Tatijana T; Lehtimäki, Terho T; Illig, Thomas T; Aspelund, Thor T; Nikopensius, Tiit T; Esko, Tonu T; Tanaka, Toshiko T; Gyllensten, Ulf U; Völker, Uwe U; Emilsson, Valur V; Vitart, Veronique V; Aalto, Ville V; Gudnason, Vilmundur V; Chouraki, Vincent V; Chen, Wei-Min WM; Igl, Wilmar W; März, Winfried W; Koenig, Wolfgang W; Lieb, Wolfgang W; Loos, Ruth J F RJ; Liu, Yongmei Y; Snieder, Harold H; Pramstaller, Peter P PP; Parsa, Afshin A; O'Connell, Jeffrey R JR; Susztak, Katalin K; Hamet, Pavel P; Tremblay, Johanne J; de Boer, Ian H IH; Böger, Carsten A CA; Goessling, Wolfram W; Chasman, Daniel I DI; Köttgen, Anna A; Kao, W H Linda WH; Fox, Caroline S CS
Genome-wide association study reveals a polymorphism in the podocyte receptor RANK for the decline of renal function in coronary patients.
Plos One
Leiherer, Andreas A; Muendlein, Axel A; Rein, Philipp P; Saely, Christoph H CH; Kinz, Elena E; Vonbank, Alexander A; Fraunberger, Peter P; Drexel, Heinz H
A gene variant in CERS2 is associated with rate of increase in albuminuria in patients with diabetes from ONTARGET and TRANSCEND.
Plos One
Shiffman, Dov D; Pare, Guillaume G; Oberbauer, Rainer R; Louie, Judy Z JZ; Rowland, Charles M CM; Devlin, James J JJ; Mann, Johannes F JF; McQueen, Matthew J MJ
Integrative biology identifies shared transcriptional networks in CKD.
Journal Of The American Society Of Nephrology : Jasn
Martini, Sebastian S; Nair, Viji V; Keller, Benjamin J BJ; Eichinger, Felix F; Hawkins, Jennifer J JJ; Randolph, Ann A; Böger, Carsten A CA; Gadegbeku, Crystal A CA; Fox, Caroline S CS; Cohen, Clemens D CD; Kretzler, Matthias M; , ; , ; ,
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
Nature Genetics
Auer, Paul L PL; Teumer, Alexander A; Schick, Ursula U; O'Shaughnessy, Andrew A; Lo, Ken Sin KS; Chami, Nathalie N; Carlson, Chris C; de Denus, Simon S; Dubé, Marie-Pierre MP; Haessler, Jeff J; Jackson, Rebecca D RD; Kooperberg, Charles C; Perreault, Louis-Philippe Lemieux LP; Nauck, Matthias M; Peters, Ulrike U; Rioux, John D JD; Schmidt, Frank F; Turcot, Valérie V; Völker, Uwe U; Völzke, Henry H; Greinacher, Andreas A; Hsu, Li L; Tardif, Jean-Claude JC; Diaz, George A GA; Reiner, Alexander P AP; Lettre, Guillaume G
Prevalence of CKD and its relationship to eGFR-related genetic loci and clinical risk factors in the SardiNIA study cohort.
Journal Of The American Society Of Nephrology : Jasn
Pani, Antonello A; Bragg-Gresham, Jennifer J; Masala, Marco M; Piras, Doloretta D; Atzeni, Alice A; Pilia, Maria G MG; Ferreli, Liana L; Balaci, Lenuta L; Curreli, Nicolò N; Delitala, Alessandro A; Loi, Francesco F; Abecasis, Gonçalo R GR; Schlessinger, David D; Cucca, Francesco F
Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.
American Journal Of Kidney Diseases : The Official Journal Of The National Kidney Foundation
Olden, Matthias M; Teumer, Alexander A; Bochud, Murielle M; Pattaro, Cristian C; Köttgen, Anna A; Turner, Stephen T ST; Rettig, Rainer R; Chen, Ming-Huei MH; Dehghan, Abbas A; Bastardot, Francois F; Schmidt, Reinhold R; Vollenweider, Peter P; Schunkert, Heribert H; Reilly, Muredach P MP; Fornage, Myriam M; Launer, Lenore J LJ; Verwoert, Germaine C GC; Mitchell, Gary F GF; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Cheng, Ching-Yu CY; Sim, Xueling X; Siscovick, David S DS; Coresh, Josef J; Kao, W H Linda WH; Fox, Caroline S CS; O'Seaghdha, Conall M CM; ,
Multiple loci associated with renal function in African Americans.
Plos One
Shriner, Daniel D; Herbert, Alan A; Doumatey, Ayo P AP; Zhou, Jie J; Huang, Hanxia H; Erdos, Michael R MR; Chen, Guanjie G; Gerry, Norman P NP; Christman, Michael F MF; Adeyemo, Adebowale A; Rotimi, Charles N CN
Validated SNPs for eGFR and their associations with albuminuria.
Human Molecular Genetics
Ellis, Jaclyn W JW; Chen, Ming-Huei MH; Foster, Meredith C MC; Liu, Ching-Ti CT; Larson, Martin G MG; de Boer, Ian I; Köttgen, Anna A; Parsa, Afshin A; Bochud, Murielle M; Böger, Carsten A CA; Kao, Linda L; Fox, Caroline S CS; O'Seaghdha, Conall M CM; , ; ,
A 4.1-Mb congenic region of Rf-4 contributes to glomerular permeability.
Journal Of The American Society Of Nephrology : Jasn
O'Meara, Caitlin C CC; Lutz, Michelle M MM; Sarkis, Allison B AB; Xu, Haiyan H; Kothinti, Rajendra K RK; Hoffman, Matthew M; Moreno, Carol C; Tabatabai, Niloofar M NM; Lazar, Jozef J; Roman, Richard J RJ; Jacob, Howard J HJ
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.
Plos Genetics
Böger, Carsten A CA; Gorski, Mathias M; Li, Man M; Hoffmann, Michael M MM; Huang, Chunmei C; Yang, Qiong Q; Teumer, Alexander A; Krane, Vera V; O'Seaghdha, Conall M CM; Kutalik, Zoltán Z; Wichmann, H-Erich HE; Haak, Thomas T; Boes, Eva E; Coassin, Stefan S; Coresh, Josef J; Kollerits, Barbara B; Haun, Margot M; Paulweber, Bernhard B; Köttgen, Anna A; Li, Guo G; Shlipak, Michael G MG; Powe, Neil N; Hwang, Shih-Jen SJ; Dehghan, Abbas A; Rivadeneira, Fernando F; Uitterlinden, André A; Hofman, Albert A; Beckmann, Jacques S JS; Krämer, Bernhard K BK; Witteman, Jacqueline J; Bochud, Murielle M; Siscovick, David D; Rettig, Rainer R; Kronenberg, Florian F; Wanner, Christoph C; Thadhani, Ravi I RI; Heid, Iris M IM; Fox, Caroline S CS; Kao, W H WH; ,
Genetic association for renal traits among participants of African ancestry reveals new loci for renal function.
Plos Genetics
Liu, Ching-Ti CT; Garnaas, Maija K MK; Tin, Adrienne A; Kottgen, Anna A; Franceschini, Nora N; Peralta, Carmen A CA; de Boer, Ian H IH; Lu, Xiaoning X; Atkinson, Elizabeth E; Ding, Jingzhong J; Nalls, Michael M; Shriner, Daniel D; Coresh, Josef J; Kutlar, Abdullah A; Bibbins-Domingo, Kirsten K; Siscovick, David D; Akylbekova, Ermeg E; Wyatt, Sharon S; Astor, Brad B; Mychaleckjy, Josef J; Li, Man M; Reilly, Muredach P MP; Townsend, Raymond R RR; Adeyemo, Adebowale A; Zonderman, Alan B AB; de Andrade, Mariza M; Turner, Stephen T ST; Mosley, Thomas H TH; Harris, Tamara B TB; , ; Rotimi, Charles N CN; Liu, Yongmei Y; Kardia, Sharon L R SL; Evans, Michele K MK; Shlipak, Michael G MG; Kramer, Holly H; Flessner, Michael F MF; Dreisbach, Albert W AW; Goessling, Wolfram W; Cupples, L Adrienne LA; Kao, W Linda WL; Fox, Caroline S CS
Journal Of The American Society Of Nephrology : Jasn
Böger, Carsten A CA; Chen, Ming-Huei MH; Tin, Adrienne A; Olden, Matthias M; Köttgen, Anna A; de Boer, Ian H IH; Fuchsberger, Christian C; O'Seaghdha, Conall M CM; Pattaro, Cristian C; Teumer, Alexander A; Liu, Ching-Ti CT; Glazer, Nicole L NL; Li, Man M; O'Connell, Jeffrey R JR; Tanaka, Toshiko T; Peralta, Carmen A CA; Kutalik, Zoltán Z; Luan, Jian'an J; Zhao, Jing Hua JH; Hwang, Shih-Jen SJ; Akylbekova, Ermeg E; Kramer, Holly H; van der Harst, Pim P; Smith, Albert V AV; Lohman, Kurt K; de Andrade, Mariza M; Hayward, Caroline C; Kollerits, Barbara B; Tönjes, Anke A; Aspelund, Thor T; Ingelsson, Erik E; Eiriksdottir, Gudny G; Launer, Lenore J LJ; Harris, Tamara B TB; Shuldiner, Alan R AR; Mitchell, Braxton D BD; Arking, Dan E DE; Franceschini, Nora N; Boerwinkle, Eric E; Egan, Josephine J; Hernandez, Dena D; Reilly, Muredach M; Townsend, Raymond R RR; Lumley, Thomas T; Siscovick, David S DS; Psaty, Bruce M BM; Kestenbaum, Bryan B; Haritunians, Talin T; Bergmann, Sven S; Vollenweider, Peter P; Waeber, Gerard G; Mooser, Vincent V; Waterworth, Dawn D; Johnson, Andrew D AD; Florez, Jose C JC; Meigs, James B JB; Lu, Xiaoning X; Turner, Stephen T ST; Atkinson, Elizabeth J EJ; Leak, Tennille S TS; Aasarød, Knut K; Skorpen, Frank F; Syvänen, Ann-Christine AC; Illig, Thomas T; Baumert, Jens J; Koenig, Wolfgang W; Krämer, Bernhard K BK; Devuyst, Olivier O; Mychaleckyj, Josyf C JC; Minelli, Cosetta C; Bakker, Stephan J L SJ; Kedenko, Lyudmyla L; Paulweber, Bernhard B; Coassin, Stefan S; Endlich, Karlhans K; Kroemer, Heyo K HK; Biffar, Reiner R; Stracke, Sylvia S; Völzke, Henry H; Stumvoll, Michael M; Mägi, Reedik R; Campbell, Harry H; Vitart, Veronique V; Hastie, Nicholas D ND; Gudnason, Vilmundur V; Kardia, Sharon L R SL; Liu, Yongmei Y; Polasek, Ozren O; Curhan, Gary G; Kronenberg, Florian F; Prokopenko, Inga I; Rudan, Igor I; Arnlöv, Johan J; Hallan, Stein S; Navis, Gerjan G; , ; Parsa, Afshin A; Ferrucci, Luigi L; Coresh, Josef J; Shlipak, Michael G MG; Bull, Shelley B SB; Paterson, Nicholas J NJ; Wichmann, H-Erich HE; Wareham, Nicholas J NJ; Loos, Ruth J F RJ; Rotter, Jerome I JI; Pramstaller, Peter P PP; Cupples, L Adrienne LA; Beckmann, Jacques S JS; Yang, Qiong Q; Heid, Iris M IM; Rettig, Rainer R; Dreisbach, Albert W AW; Bochud, Murielle M; Fox, Caroline S CS; Kao, W H L WH
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.
Plos Genetics
Gudbjartsson, Daniel F DF; Holm, Hilma H; Indridason, Olafur S OS; Thorleifsson, Gudmar G; Edvardsson, Vidar V; Sulem, Patrick P; de Vegt, Femmie F; d'Ancona, Frank C H FC; den Heijer, Martin M; Wetzels, Jack F M JF; Franzson, Leifur L; Rafnar, Thorunn T; Kristjansson, Kristleifur K; Bjornsdottir, Unnur S US; Eyjolfsson, Gudmundur I GI; Kiemeney, Lambertus A LA; Kong, Augustine A; Palsson, Runolfur R; Thorsteinsdottir, Unnur U; Stefansson, Kari K
Genetic loci influencing kidney function and chronic kidney disease.
Nature Genetics
Chambers, John C JC; Zhang, Weihua W; Lord, Graham M GM; van der Harst, Pim P; Lawlor, Debbie A DA; Sehmi, Joban S JS; Gale, Daniel P DP; Wass, Mark N MN; Ahmadi, Kourosh R KR; Bakker, Stephan J L SJ; Beckmann, Jacqui J; Bilo, Henk J G HJ; Bochud, Murielle M; Brown, Morris J MJ; Caulfield, Mark J MJ; Connell, John M C JM; Cook, H Terence HT; Cotlarciuc, Ioana I; Davey Smith, George G; de Silva, Ranil R; Deng, Guohong G; Devuyst, Olivier O; Dikkeschei, Lambert D LD; Dimkovic, Nada N; Dockrell, Mark M; Dominiczak, Anna A; Ebrahim, Shah S; Eggermann, Thomas T; Farrall, Martin M; Ferrucci, Luigi L; Floege, Jurgen J; Forouhi, Nita G NG; Gansevoort, Ron T RT; Han, Xijin X; Hedblad, Bo B; Homan van der Heide, Jaap J JJ; Hepkema, Bouke G BG; Hernandez-Fuentes, Maria M; Hypponen, Elina E; Johnson, Toby T; de Jong, Paul E PE; Kleefstra, Nanne N; Lagou, Vasiliki V; Lapsley, Marta M; Li, Yun Y; Loos, Ruth J F RJ; Luan, Jian'an J; Luttropp, Karin K; Maréchal, Céline C; Melander, Olle O; Munroe, Patricia B PB; Nordfors, Louise L; Parsa, Afshin A; Peltonen, Leena L; Penninx, Brenda W BW; Perucha, Esperanza E; Pouta, Anneli A; Prokopenko, Inga I; Roderick, Paul J PJ; Ruokonen, Aimo A; Samani, Nilesh J NJ; Sanna, Serena S; Schalling, Martin M; Schlessinger, David D; Schlieper, Georg G; Seelen, Marc A J MA; Shuldiner, Alan R AR; Sjögren, Marketa M; Smit, Johannes H JH; Snieder, Harold H; Soranzo, Nicole N; Spector, Timothy D TD; Stenvinkel, Peter P; Sternberg, Michael J E MJ; Swaminathan, Ramasamyiyer R; Tanaka, Toshiko T; Ubink-Veltmaat, Lielith J LJ; Uda, Manuela M; Vollenweider, Peter P; Wallace, Chris C; Waterworth, Dawn D; Zerres, Klaus K; Waeber, Gerard G; Wareham, Nicholas J NJ; Maxwell, Patrick H PH; McCarthy, Mark I MI; Jarvelin, Marjo-Riitta MR; Mooser, Vincent V; Abecasis, Goncalo R GR; Lightstone, Liz L; Scott, James J; Navis, Gerjan G; Elliott, Paul P; Kooner, Jaspal S JS
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level.
Bmc Medical Genetics
Pattaro, Cristian C; De Grandi, Alessandro A; Vitart, Veronique V; Hayward, Caroline C; Franke, Andre A; Aulchenko, Yurii S YS; Johansson, Asa A; Wild, Sarah H SH; Melville, Scott A SA; Isaacs, Aaron A; Polasek, Ozren O; Ellinghaus, David D; Kolcic, Ivana I; Nöthlings, Ute U; Zgaga, Lina L; Zemunik, Tatijana T; Gnewuch, Carsten C; Schreiber, Stefan S; Campbell, Susan S; Hastie, Nick N; Boban, Mladen M; Meitinger, Thomas T; Oostra, Ben A BA; Riegler, Peter P; Minelli, Cosetta C; Wright, Alan F AF; Campbell, Harry H; van Duijn, Cornelia M CM; Gyllensten, Ulf U; Wilson, James F JF; Krawczak, Michael M; Rudan, Igor I; Pramstaller, Peter P PP; ,
Multiple loci associated with indices of renal function and chronic kidney disease.
Nature Genetics
Köttgen, Anna A; Glazer, Nicole L NL; Dehghan, Abbas A; Hwang, Shih-Jen SJ; Katz, Ronit R; Li, Man M; Yang, Qiong Q; Gudnason, Vilmundur V; Launer, Lenore J LJ; Harris, Tamara B TB; Smith, Albert V AV; Arking, Dan E DE; Astor, Brad C BC; Boerwinkle, Eric E; Ehret, Georg B GB; Ruczinski, Ingo I; Scharpf, Robert B RB; Chen, Yii-Der Ida YD; de Boer, Ian H IH; Haritunians, Talin T; Lumley, Thomas T; Sarnak, Mark M; Siscovick, David D; Benjamin, Emelia J EJ; Levy, Daniel D; Upadhyay, Ashish A; Aulchenko, Yurii S YS; Hofman, Albert A; Rivadeneira, Fernando F; Uitterlinden, André G AG; van Duijn, Cornelia M CM; Chasman, Daniel I DI; Paré, Guillaume G; Ridker, Paul M PM; Kao, W H Linda WH; Witteman, Jacqueline C JC; Coresh, Josef J; Shlipak, Michael G MG; Fox, Caroline S CS