Type 2 Diabetes-Related Variants Influence the Risk of Developing Prostate Cancer: A Population-Based Case-Control Study and Meta-Analysis.
Cancers
Sánchez-Maldonado, José Manuel JM; Collado, Ricardo R; Cabrera-Serrano, Antonio José AJ; Ter Horst, Rob R; Gálvez-Montosa, Fernando F; Robles-Fernández, Inmaculada I; Arenas-Rodríguez, Verónica V; Cano-Gutiérrez, Blanca B; Bakker, Olivier O; Bravo-Fernández, María Inmaculada MI; García-Verdejo, Francisco José FJ; López, José Antonio López JAL; Olivares-Ruiz, Jesús J; López-Nevot, Miguel Ángel MÁ; Fernández-Puerta, Laura L; Cózar-Olmo, José Manuel JM; Li, Yang Y; Netea, Mihai G MG; Jurado, Manuel M; Lorente, Jose Antonio JA; Sánchez-Rovira, Pedro P; Álvarez-Cubero, María Jesús MJ; Sainz, Juan J
Functional characterization of T2D-associated SNP effects on baseline and ER stress-responsive β cell transcriptional activation.
Nature Communications
Khetan, Shubham S; Kales, Susan S; Kursawe, Romy R; Jillette, Alexandria A; Ulirsch, Jacob C JC; Reilly, Steven K SK; Ucar, Duygu D; Tewhey, Ryan R; Stitzel, Michael L ML
All thresholds of maternal hyperglycaemia from the WHO 2013 criteria for gestational diabetes identify women with a higher genetic risk for type 2 diabetes.
Wellcome Open Research
Hughes, Alice E AE; Hayes, M Geoffrey MG; Egan, Aoife M AM; Patel, Kashyap A KA; Scholtens, Denise M DM; Lowe, Lynn P LP; Lowe, William L WL; Dunne, Fidelma P FP; Hattersley, Andrew T AT; Freathy, Rachel M RM
Genetic factors and risk of type 2 diabetes among women with a history of gestational diabetes: findings from two independent populations.
Bmj Open Diabetes Research & Care
Li, Mengying M; Rahman, Mohammad L ML; Wu, Jing J; Ding, Ming M; Chavarro, Jorge E JE; Lin, Yuan Y; Ley, Sylvia H SH; Bao, Wei W; Grunnet, Louise G LG; Hinkle, Stefanie N SN; Thuesen, Anne Cathrine B ACB; Yeung, Edwina E; Gore-Langton, Robert E RE; Sherman, Seth S; Hjort, Line L; Kampmann, Freja Bach FB; Bjerregaard, Anne Ahrendt AA; Damm, Peter P; Tekola-Ayele, Fasil F; Liu, Aiyi A; Mills, James L JL; Vaag, Allan A; Olsen, Sjurdur F SF; Hu, Frank B FB; Zhang, Cuilin C
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
Nature
Flannick, Jason J; Mercader, Josep M JM; Fuchsberger, Christian C; Udler, Miriam S MS; Mahajan, Anubha A; Wessel, Jennifer J; Teslovich, Tanya M TM; Caulkins, Lizz L; Koesterer, Ryan R; Barajas-Olmos, Francisco F; Blackwell, Thomas W TW; Boerwinkle, Eric E; Brody, Jennifer A JA; Centeno-Cruz, Federico F; Chen, Ling L; Chen, Siying S; Contreras-Cubas, Cecilia C; Córdova, Emilio E; Correa, Adolfo A; Cortes, Maria M; DeFronzo, Ralph A RA; Dolan, Lawrence L; Drews, Kimberly L KL; Elliott, Amanda A; Floyd, James S JS; Gabriel, Stacey S; Garay-Sevilla, Maria Eugenia ME; García-Ortiz, Humberto H; Gross, Myron M; Han, Sohee S; Heard-Costa, Nancy L NL; Jackson, Anne U AU; Jørgensen, Marit E ME; Kang, Hyun Min HM; Kelsey, Megan M; Kim, Bong-Jo BJ; Koistinen, Heikki A HA; Kuusisto, Johanna J; Leader, Joseph B JB; Linneberg, Allan A; Liu, Ching-Ti CT; Liu, Jianjun J; Lyssenko, Valeriya V; Manning, Alisa K AK; Marcketta, Anthony A; Malacara-Hernandez, Juan Manuel JM; Martínez-Hernández, Angélica A; Matsuo, Karen K; Mayer-Davis, Elizabeth E; Mendoza-Caamal, Elvia E; Mohlke, Karen L KL; Morrison, Alanna C AC; Ndungu, Anne A; Ng, Maggie C Y MCY; O'Dushlaine, Colm C; Payne, Anthony J AJ; Pihoker, Catherine C; , ; Post, Wendy S WS; Preuss, Michael M; Psaty, Bruce M BM; Vasan, Ramachandran S RS; Rayner, N William NW; Reiner, Alexander P AP; Revilla-Monsalve, Cristina C; Robertson, Neil R NR; Santoro, Nicola N; Schurmann, Claudia C; So, Wing Yee WY; Soberón, Xavier X; Stringham, Heather M HM; Strom, Tim M TM; Tam, Claudia H T CHT; Thameem, Farook F; Tomlinson, Brian B; Torres, Jason M JM; Tracy, Russell P RP; van Dam, Rob M RM; Vujkovic, Marijana M; Wang, Shuai S; Welch, Ryan P RP; Witte, Daniel R DR; Wong, Tien-Yin TY; Atzmon, Gil G; Barzilai, Nir N; Blangero, John J; Bonnycastle, Lori L LL; Bowden, Donald W DW; Chambers, John C JC; Chan, Edmund E; Cheng, Ching-Yu CY; Cho, Yoon Shin YS; Collins, Francis S FS; de Vries, Paul S PS; Duggirala, Ravindranath R; Glaser, Benjamin B; Gonzalez, Clicerio C; Gonzalez, Ma Elena ME; Groop, Leif L; Kooner, Jaspal Singh JS; Kwak, Soo Heon SH; Laakso, Markku M; Lehman, Donna M DM; Nilsson, Peter P; Spector, Timothy D TD; Tai, E Shyong ES; Tuomi, Tiinamaija T; Tuomilehto, Jaakko J; Wilson, James G JG; Aguilar-Salinas, Carlos A CA; Bottinger, Erwin E; Burke, Brian B; Carey, David J DJ; Chan, Juliana C N JCN; Dupuis, Josée J; Frossard, Philippe P; Heckbert, Susan R SR; Hwang, Mi Yeong MY; Kim, Young Jin YJ; Kirchner, H Lester HL; Lee, Jong-Young JY; Lee, Juyoung J; Loos, Ruth J F RJF; Ma, Ronald C W RCW; Morris, Andrew D AD; O'Donnell, Christopher J CJ; Palmer, Colin N A CNA; Pankow, James J; Park, Kyong Soo KS; Rasheed, Asif A; Saleheen, Danish D; Sim, Xueling X; Small, Kerrin S KS; Teo, Yik Ying YY; Haiman, Christopher C; Hanis, Craig L CL; Henderson, Brian E BE; Orozco, Lorena L; Tusié-Luna, Teresa T; Dewey, Frederick E FE; Baras, Aris A; Gieger, Christian C; Meitinger, Thomas T; Strauch, Konstantin K; Lange, Leslie L; Grarup, Niels N; Hansen, Torben T; Pedersen, Oluf O; Zeitler, Philip P; Dabelea, Dana D; Abecasis, Goncalo G; Bell, Graeme I GI; Cox, Nancy J NJ; Seielstad, Mark M; Sladek, Rob R; Meigs, James B JB; Rich, Steve S SS; Rotter, Jerome I JI; , ; , ; , ; , ; , ; , ; , ; , ; , ; Altshuler, David D; Burtt, Noël P NP; Scott, Laura J LJ; Morris, Andrew P AP; Florez, Jose C JC; McCarthy, Mark I MI; Boehnke, Michael M
Genetic contributions to lupus nephritis in a multi-ethnic cohort of systemic lupus erythematous patients.
Plos One
Lanata, Cristina M CM; Nititham, Joanne J; Taylor, Kimberly E KE; Chung, Sharon A SA; Torgerson, Dara G DG; Seldin, Michael F MF; Pons-Estel, Bernardo A BA; Tusié-Luna, Teresa T; Tsao, Betty P BP; Morand, Eric F EF; Alarcón-Riquelme, Marta E ME; Criswell, Lindsey A LA
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.
Nature Genetics
Hysi, Pirro G PG; Valdes, Ana M AM; Liu, Fan F; Furlotte, Nicholas A NA; Evans, David M DM; Bataille, Veronique V; Visconti, Alessia A; Hemani, Gibran G; McMahon, George G; Ring, Susan M SM; Smith, George Davey GD; Duffy, David L DL; Zhu, Gu G; Gordon, Scott D SD; Medland, Sarah E SE; Lin, Bochao D BD; Willemsen, Gonneke G; Jan Hottenga, Jouke J; Vuckovic, Dragana D; Girotto, Giorgia G; Gandin, Ilaria I; Sala, Cinzia C; Concas, Maria Pina MP; Brumat, Marco M; Gasparini, Paolo P; Toniolo, Daniela D; Cocca, Massimiliano M; Robino, Antonietta A; Yazar, Seyhan S; Hewitt, Alex W AW; Chen, Yan Y; Zeng, Changqing C; Uitterlinden, Andre G AG; Ikram, M Arfan MA; Hamer, Merel A MA; van Duijn, Cornelia M CM; Nijsten, Tamar T; Mackey, David A DA; Falchi, Mario M; Boomsma, Dorret I DI; Martin, Nicholas G NG; , ; Hinds, David A DA; Kayser, Manfred M; Spector, Timothy D TD
Fine-mapping inflammatory bowel disease loci to single-variant resolution.
Nature
Huang, Hailiang H; Fang, Ming M; Jostins, Luke L; Umićević Mirkov, Maša M; Boucher, Gabrielle G; Anderson, Carl A CA; Andersen, Vibeke V; Cleynen, Isabelle I; Cortes, Adrian A; Crins, François F; D'Amato, Mauro M; Deffontaine, Valérie V; Dmitrieva, Julia J; Docampo, Elisa E; Elansary, Mahmoud M; Farh, Kyle Kai-How KK; Franke, Andre A; Gori, Ann-Stephan AS; Goyette, Philippe P; Halfvarson, Jonas J; Haritunians, Talin T; Knight, Jo J; Lawrance, Ian C IC; Lees, Charlie W CW; Louis, Edouard E; Mariman, Rob R; Meuwissen, Theo T; Mni, Myriam M; Momozawa, Yukihide Y; Parkes, Miles M; Spain, Sarah L SL; Théâtre, Emilie E; Trynka, Gosia G; Satsangi, Jack J; van Sommeren, Suzanne S; Vermeire, Severine S; Xavier, Ramnik J RJ; , ; Weersma, Rinse K RK; Duerr, Richard H RH; Mathew, Christopher G CG; Rioux, John D JD; McGovern, Dermot P B DPB; Cho, Judy H JH; Georges, Michel M; Daly, Mark J MJ; Barrett, Jeffrey C JC
Discovery of novel heart rate-associated loci using the Exome Chip.
Human Molecular Genetics
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Interactome-transcriptome analysis discovers signatures complementary to GWAS Loci of Type 2 Diabetes.
Scientific Reports
Li, Jing-Woei JW; Lee, Heung-Man HM; Wang, Ying Y; Tong, Amy Hin-Yan AH; Yip, Kevin Y KY; Tsui, Stephen Kwok-Wing SK; Lok, Si S; Ozaki, Risa R; Luk, Andrea O AO; Kong, Alice P S AP; So, Wing-Yee WY; Ma, Ronald C W RC; Chan, Juliana C N JC; Chan, Ting-Fung TF
General Framework for Meta-Analysis of Haplotype Association Tests.
Genetic Epidemiology
Wang, Shuai S; Zhao, Jing Hua JH; An, Ping P; Guo, Xiuqing X; Jensen, Richard A RA; Marten, Jonathan J; Huffman, Jennifer E JE; Meidtner, Karina K; Boeing, Heiner H; Campbell, Archie A; Rice, Kenneth M KM; Scott, Robert A RA; Yao, Jie J; Schulze, Matthias B MB; Wareham, Nicholas J NJ; Borecki, Ingrid B IB; Province, Michael A MA; Rotter, Jerome I JI; Hayward, Caroline C; Goodarzi, Mark O MO; Meigs, James B JB; Dupuis, Josée J
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis.
Frontiers In Genetics
Namjou, Bahram B; Marsolo, Keith K; Caroll, Robert J RJ; Denny, Joshua C JC; Ritchie, Marylyn D MD; Verma, Shefali S SS; Lingren, Todd T; Porollo, Aleksey A; Cobb, Beth L BL; Perry, Cassandra C; Kottyan, Leah C LC; Rothenberg, Marc E ME; Thompson, Susan D SD; Holm, Ingrid A IA; Kohane, Isaac S IS; Harley, John B JB
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
Nature Genetics
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A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
Human Molecular Genetics
Martin, Jose-Ezequiel JE; Assassi, Shervin S; Diaz-Gallo, Lina-Marcela LM; Broen, Jasper C JC; Simeon, Carmen P CP; Castellvi, Ivan I; Vicente-Rabaneda, Esther E; Fonollosa, Vicente V; Ortego-Centeno, Norberto N; González-Gay, Miguel A MA; Espinosa, Gerard G; Carreira, Patricia P; , ; , ; , ; , ; Camps, Mayte M; Sabio, Jose M JM; D'alfonso, Sandra S; Vonk, Madelon C MC; Voskuyl, Alexandre E AE; Schuerwegh, Annemie J AJ; Kreuter, Alexander A; Witte, Torsten T; Riemekasten, Gabriella G; Hunzelmann, Nicolas N; Airo, Paolo P; Beretta, Lorenzo L; Scorza, Raffaella R; Lunardi, Claudio C; Van Laar, Jacob J; Chee, Meng May MM; Worthington, Jane J; Herrick, Arianne A; Denton, Christopher C; Fonseca, Carmen C; Tan, Filemon K FK; Arnett, Frank F; Zhou, Xiaodong X; Reveille, John D JD; Gorlova, Olga O; Koeleman, Bobby P C BP; Radstake, Timothy R D J TR; Vyse, Timothy T; Mayes, Maureen D MD; Alarcón-Riquelme, Marta E ME; Martin, Javier J
Allele-specific transcriptional activity at type 2 diabetes-associated single nucleotide polymorphisms in regions of pancreatic islet open chromatin at the JAZF1 locus.
Diabetes
Fogarty, Marie P MP; Panhuis, Tami M TM; Vadlamudi, Swarooparani S; Buchkovich, Martin L ML; Mohlke, Karen L KL
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.
Plos Genetics
Chung, Sharon A SA; Taylor, Kimberly E KE; Graham, Robert R RR; Nititham, Joanne J; Lee, Annette T AT; Ortmann, Ward A WA; Jacob, Chaim O CO; Alarcón-Riquelme, Marta E ME; Tsao, Betty P BP; Harley, John B JB; Gaffney, Patrick M PM; Moser, Kathy L KL; , ; Petri, Michelle M; Demirci, F Yesim FY; Kamboh, M Ilyas MI; Manzi, Susan S; Gregersen, Peter K PK; Langefeld, Carl D CD; Behrens, Timothy W TW; Criswell, Lindsey A LA
Risk alleles for systemic lupus erythematosus in a large case-control collection and associations with clinical subphenotypes.
Plos Genetics
Taylor, Kimberly E KE; Chung, Sharon A SA; Graham, Robert R RR; Ortmann, Ward A WA; Lee, Annette T AT; Langefeld, Carl D CD; Jacob, Chaim O CO; Kamboh, M Ilyas MI; Alarcón-Riquelme, Marta E ME; Tsao, Betty P BP; Moser, Kathy L KL; Gaffney, Patrick M PM; Harley, John B JB; Petri, Michelle M; Manzi, Susan S; Gregersen, Peter K PK; Behrens, Timothy W TW; Criswell, Lindsey A LA
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
Nature Genetics
Voight, Benjamin F BF; Scott, Laura J LJ; Steinthorsdottir, Valgerdur V; Morris, Andrew P AP; Dina, Christian C; Welch, Ryan P RP; Zeggini, Eleftheria E; Huth, Cornelia C; Aulchenko, Yurii S YS; Thorleifsson, Gudmar G; McCulloch, Laura J LJ; Ferreira, Teresa T; Grallert, Harald H; Amin, Najaf N; Wu, Guanming G; Willer, Cristen J CJ; Raychaudhuri, Soumya S; McCarroll, Steve A SA; Langenberg, Claudia C; Hofmann, Oliver M OM; Dupuis, Josée J; Qi, Lu L; Segrè, Ayellet V AV; van Hoek, Mandy M; Navarro, Pau P; Ardlie, Kristin K; Balkau, Beverley B; Benediktsson, Rafn R; Bennett, Amanda J AJ; Blagieva, Roza R; Boerwinkle, Eric E; Bonnycastle, Lori L LL; Bengtsson Boström, Kristina K; Bravenboer, Bert B; Bumpstead, Suzannah S; Burtt, Noisël P NP; Charpentier, Guillaume G; Chines, Peter S PS; Cornelis, Marilyn M; Couper, David J DJ; Crawford, Gabe G; Doney, Alex S F AS; Elliott, Katherine S KS; Elliott, Amanda L AL; Erdos, Michael R MR; Fox, Caroline S CS; Franklin, Christopher S CS; Ganser, Martha M; Gieger, Christian C; Grarup, Niels N; Green, Todd T; Griffin, Simon S; Groves, Christopher J CJ; Guiducci, Candace C; Hadjadj, Samy S; Hassanali, Neelam N; Herder, Christian C; Isomaa, Bo B; Jackson, Anne U AU; Johnson, Paul R V PR; Jørgensen, Torben T; Kao, Wen H L WH; Klopp, Norman N; Kong, Augustine A; Kraft, Peter P; Kuusisto, Johanna J; Lauritzen, Torsten T; Li, Man M; Lieverse, Aloysius A; Lindgren, Cecilia M CM; Lyssenko, Valeriya V; Marre, Michel M; Meitinger, Thomas T; Midthjell, Kristian K; Morken, Mario A MA; Narisu, Narisu N; Nilsson, Peter P; Owen, Katharine R KR; Payne, Felicity F; Perry, John R B JR; Petersen, Ann-Kristin AK; Platou, Carl C; Proença, Christine C; Prokopenko, Inga I; Rathmann, Wolfgang W; Rayner, N William NW; Robertson, Neil R NR; Rocheleau, Ghislain G; Roden, Michael M; Sampson, Michael J MJ; Saxena, Richa R; Shields, Beverley M BM; Shrader, Peter P; Sigurdsson, Gunnar G; Sparsø, Thomas T; Strassburger, Klaus K; Stringham, Heather M HM; Sun, Qi Q; Swift, Amy J AJ; Thorand, Barbara B; Tichet, Jean J; Tuomi, Tiinamaija T; van Dam, Rob M RM; van Haeften, Timon W TW; van Herpt, Thijs T; van Vliet-Ostaptchouk, Jana V JV; Walters, G Bragi GB; Weedon, Michael N MN; Wijmenga, Cisca C; Witteman, Jacqueline J; Bergman, Richard N RN; Cauchi, Stephane S; Collins, Francis S FS; Gloyn, Anna L AL; Gyllensten, Ulf U; Hansen, Torben T; Hide, Winston A WA; Hitman, Graham A GA; Hofman, Albert A; Hunter, David J DJ; Hveem, Kristian K; Laakso, Markku M; Mohlke, Karen L KL; Morris, Andrew D AD; Palmer, Colin N A CN; Pramstaller, Peter P PP; Rudan, Igor I; Sijbrands, Eric E; Stein, Lincoln D LD; Tuomilehto, Jaakko J; Uitterlinden, Andre A; Walker, Mark M; Wareham, Nicholas J NJ; Watanabe, Richard M RM; Abecasis, Gonçalo R GR; Boehm, Bernhard O BO; Campbell, Harry H; Daly, Mark J MJ; Hattersley, Andrew T AT; Hu, Frank B FB; Meigs, James B JB; Pankow, James S JS; Pedersen, Oluf O; Wichmann, H-Erich HE; Barroso, Inês I; Florez, Jose C JC; Frayling, Timothy M TM; Groop, Leif L; Sladek, Rob R; Thorsteinsdottir, Unnur U; Wilson, James F JF; Illig, Thomas T; Froguel, Philippe P; van Duijn, Cornelia M CM; Stefansson, Kari K; Altshuler, David D; Boehnke, Michael M; McCarthy, Mark I MI; , ; ,
Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.
Diabetes
Zhao, Jianhua J; Bradfield, Jonathan P JP; Zhang, Haitao H; Annaiah, Kiran K; Wang, Kai K; Kim, Cecilia E CE; Glessner, Joseph T JT; Frackelton, Edward C EC; Otieno, F George FG; Doran, James J; Thomas, Kelly A KA; Garris, Maria M; Hou, Cuiping C; Chiavacci, Rosetta M RM; Li, Mingyao M; Berkowitz, Robert I RI; Hakonarson, Hakon H; Grant, Struan F A SF
Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.
Diabetes
Zhao, Jianhua J; Li, Mingyao M; Bradfield, Jonathan P JP; Wang, Kai K; Zhang, Haitao H; Sleiman, Patrick P; Kim, Cecilia E CE; Annaiah, Kiran K; Glaberson, Wendy W; Glessner, Joseph T JT; Otieno, F George FG; Thomas, Kelly A KA; Garris, Maria M; Hou, Cuiping C; Frackelton, Edward C EC; Chiavacci, Rosetta M RM; Berkowitz, Robert I RI; Hakonarson, Hakon H; Grant, Struan F A SF
Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.
Plos Genetics
Paré, Guillaume G; Chasman, Daniel I DI; Parker, Alexander N AN; Nathan, David M DM; Miletich, Joseph P JP; Zee, Robert Y RY; Ridker, Paul M PM
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.
Human Molecular Genetics
Johansson, Asa A; Marroni, Fabio F; Hayward, Caroline C; Franklin, Christopher S CS; Kirichenko, Anatoly V AV; Jonasson, Inger I; Hicks, Andrew A AA; Vitart, Veronique V; Isaacs, Aaron A; Axenovich, Tatiana T; Campbell, Susan S; Dunlop, Malcolm G MG; Floyd, Jamie J; Hastie, Nick N; Hofman, Albert A; Knott, Sara S; Kolcic, Ivana I; Pichler, Irene I; Polasek, Ozren O; Rivadeneira, Fernando F; Tenesa, Albert A; Uitterlinden, André G AG; Wild, Sarah H SH; Zorkoltseva, Irina V IV; Meitinger, Thomas T; Wilson, James F JF; Rudan, Igor I; Campbell, Harry H; Pattaro, Cristian C; Pramstaller, Peter P; Oostra, Ben A BA; Wright, Alan F AF; van Duijn, Cornelia M CM; Aulchenko, Yurii S YS; Gyllensten, Ulf U; ,
Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study.
Diabetes
van Hoek, Mandy M; Dehghan, Abbas A; Witteman, Jacqueline C M JC; van Duijn, Cornelia M CM; Uitterlinden, André G AG; Oostra, Ben A BA; Hofman, Albert A; Sijbrands, Eric J G EJ; Janssens, A Cecile J W AC
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.
Blood
Cooper, Gregory M GM; Johnson, Julie A JA; Langaee, Taimour Y TY; Feng, Hua H; Stanaway, Ian B IB; Schwarz, Ute I UI; Ritchie, Marylyn D MD; Stein, C Michael CM; Roden, Dan M DM; Smith, Joshua D JD; Veenstra, David L DL; Rettie, Allan E AE; Rieder, Mark J MJ