Identifying genetic variants for amyloid β in subcortical vascular cognitive impairment.
Frontiers In Aging Neuroscience
Kim, Hang-Rai HR; Jung, Sang-Hyuk SH; Kim, Beomsu B; Kim, Jaeho J; Jang, Hyemin H; Kim, Jun Pyo JP; Kim, So Yeon SY; Na, Duk L DL; Kim, Hee Jin HJ; Nho, Kwangsik K; Won, Hong-Hee HH; Seo, Sang Won SW
Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.
Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Aldehyde dehydrogenase 2 polymorphism is associated with chemotherapy-related cognitive impairment in patients with breast cancer who receive chemotherapy.
Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study.
Journal Of Alzheimer'S Disease : Jad
Kang, Sarang S; Gim, Jungsoo J; Lee, Jiwoon J; Gunasekaran, Tamil Iniyan TI; Choi, Kyu Yeong KY; Lee, Jang Jae JJ; Seo, Eun Hyun EH; Ko, Pan-Woo PW; Chung, Ji Yeon JY; Choi, Seong-Min SM; Lee, Young Min YM; Jeong, Jee Hyang JH; Park, Kyung Won KW; Song, Min Kyung MK; Lee, Ho-Won HW; Kim, Ki Woong KW; Choi, Seong Hye SH; Lee, Dong Young DY; Kim, Sang Yun SY; Kim, Hoowon H; Kim, Byeong C BC; Ikeuchi, Takeshi T; Lee, Kun Ho KH
Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease.
Acta Neuropathologica Communications
Reddy, Joseph S JS; Allen, Mariet M; Ho, Charlotte C G CCG; Oatman, Stephanie R SR; İş, Özkan Ö; Quicksall, Zachary S ZS; Wang, Xue X; Jin, Jiangli J; Patel, Tulsi A TA; Carnwath, Troy P TP; Nguyen, Thuy T TT; Malphrus, Kimberly G KG; Lincoln, Sarah J SJ; Carrasquillo, Minerva M MM; Crook, Julia E JE; Kanekiyo, Takahisa T; Murray, Melissa E ME; Bu, Guojun G; Dickson, Dennis W DW; Ertekin-Taner, Nilüfer N
Genome-wide association study of high-sensitivity C-reactive protein, D-dimer, and interleukin-6 levels in multiethnic HIV+ cohorts.
Aids (London, England)
Sherman, Brad T BT; Hu, Xiaojun X; Singh, Kanal K; Haine, Lillian L; Rupert, Adam W AW; Neaton, James D JD; Lundgren, Jens D JD; Imamichi, Tomozumi T; Chang, Weizhong W; Lane, H Clifford HC; ,
Effect of apolipoprotein E polymorphism on cognition and brain in the Cambridge Centre for Ageing and Neuroscience cohort.
Brain And Neuroscience Advances
Henson, Richard N RN; Suri, Sana S; Knights, Ethan E; Rowe, James B JB; Kievit, Rogier A RA; Lyall, Donald M DM; Chan, Dennis D; Eising, Else E; Fisher, Simon E SE
Genetic and polygenic risk score analysis for Alzheimer's disease in the Chinese population.
Alzheimer'S & Dementia (Amsterdam, Netherlands)
Zhou, Xiaopu X; Chen, Yu Y; Ip, Fanny C F FCF; Lai, Nicole C H NCH; Li, Yolanda Y T YYT; Jiang, Yuanbing Y; Zhong, Huan H; Chen, Yuewen Y; Zhang, Yulin Y; Ma, Shuangshuang S; Lo, Ronnie M N RMN; Cheung, Kit K; Tong, Estella P S EPS; Ko, Ho H; Shoai, Maryam M; Mok, Kin Y KY; Hardy, John J; Mok, Vincent C T VCT; Kwok, Timothy C Y TCY; Fu, Amy K Y AKY; Ip, Nancy Y NY
Non-coding variability at the APOE locus contributes to the Alzheimer's risk.
Nature Communications
Zhou, Xiaopu X; Chen, Yu Y; Mok, Kin Y KY; Kwok, Timothy C Y TCY; Mok, Vincent C T VCT; Guo, Qihao Q; Ip, Fanny C FC; Chen, Yuewen Y; Mullapudi, Nandita N; , ; Giusti-Rodríguez, Paola P; Sullivan, Patrick F PF; Hardy, John J; Fu, Amy K Y AKY; Li, Yun Y; Ip, Nancy Y NY
Association between APOE e4 and white matter hyperintensity volume, but not total brain volume or white matter integrity.
Brain Imaging And Behavior
Lyall, Donald M DM; Cox, Simon R SR; Lyall, Laura M LM; Celis-Morales, Carlos C; Cullen, Breda B; Mackay, Daniel F DF; Ward, Joey J; Strawbridge, Rona J RJ; McIntosh, Andrew M AM; Sattar, Naveed N; Smith, Daniel J DJ; Cavanagh, Jonathan J; Deary, Ian J IJ; Pell, Jill P JP
Biothiols and oxidative stress markers and polymorphisms of TOMM40 and APOC1 genes in Alzheimer's disease patients.
Oncotarget
Prendecki, Michal M; Florczak-Wyspianska, Jolanta J; Kowalska, Marta M; Ilkowski, Jan J; Grzelak, Teresa T; Bialas, Katarzyna K; Wiszniewska, Malgorzata M; Kozubski, Wojciech W; Dorszewska, Jolanta J
Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging.
Molecular Psychiatry
Yan, Qi Q; Nho, Kwangsik K; Del-Aguila, Jorge L JL; Wang, Xingbin X; Risacher, Shannon L SL; Fan, Kang-Hsien KH; Snitz, Beth E BE; Aizenstein, Howard J HJ; Mathis, Chester A CA; Lopez, Oscar L OL; Demirci, F Yesim FY; Feingold, Eleanor E; Klunk, William E WE; Saykin, Andrew J AJ; , ; Cruchaga, Carlos C; Kamboh, M Ilyas MI
Marioni, Riccardo E RE; Harris, Sarah E SE; Zhang, Qian Q; McRae, Allan F AF; Hagenaars, Saskia P SP; Hill, W David WD; Davies, Gail G; Ritchie, Craig W CW; Gale, Catharine R CR; Starr, John M JM; Goate, Alison M AM; Porteous, David J DJ; Yang, Jian J; Evans, Kathryn L KL; Deary, Ian J IJ; Wray, Naomi R NR; Visscher, Peter M PM
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
Molecular Psychiatry
Trampush, J W JW; Yang, M L Z ML; Yu, J J; Knowles, E E; Davies, G G; Liewald, D C DC; Starr, J M JM; Djurovic, S S; Melle, I I; Sundet, K K; Christoforou, A A; Reinvang, I I; DeRosse, P P; Lundervold, A J AJ; Steen, V M VM; Espeseth, T T; Räikkönen, K K; Widen, E E; Palotie, A A; Eriksson, J G JG; Giegling, I I; Konte, B B; Roussos, P P; Giakoumaki, S S; Burdick, K E KE; Payton, A A; Ollier, W W; Horan, M M; Chiba-Falek, O O; Attix, D K DK; Need, A C AC; Cirulli, E T ET; Voineskos, A N AN; Stefanis, N C NC; Avramopoulos, D D; Hatzimanolis, A A; Arking, D E DE; Smyrnis, N N; Bilder, R M RM; Freimer, N A NA; Cannon, T D TD; London, E E; Poldrack, R A RA; Sabb, F W FW; Congdon, E E; Conley, E D ED; Scult, M A MA; Dickinson, D D; Straub, R E RE; Donohoe, G G; Morris, D D; Corvin, A A; Gill, M M; Hariri, A R AR; Weinberger, D R DR; Pendleton, N N; Bitsios, P P; Rujescu, D D; Lahti, J J; Le Hellard, S S; Keller, M C MC; Andreassen, O A OA; Deary, I J IJ; Glahn, D C DC; Malhotra, A K AK; Lencz, T T
Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences.
Intelligence
Hill, W D WD; Davies, G G; Liewald, D C DC; Payton, A A; McNeil, C J CJ; Whalley, L J LJ; Horan, M M; Ollier, W W; Starr, J M JM; Pendleton, N N; Hansel, N K NK; Montgomery, G W GW; Medland, S E SE; Martin, N G NG; Wright, M J MJ; Bates, T C TC; Deary, I J IJ
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.
Nature Communications
Lu, Yingchang Y; Day, Felix R FR; Gustafsson, Stefan S; Buchkovich, Martin L ML; Na, Jianbo J; Bataille, Veronique V; Cousminer, Diana L DL; Dastani, Zari Z; Drong, Alexander W AW; Esko, Tõnu T; Evans, David M DM; Falchi, Mario M; Feitosa, Mary F MF; Ferreira, Teresa T; Hedman, Åsa K ÅK; Haring, Robin R; Hysi, Pirro G PG; Iles, Mark M MM; Justice, Anne E AE; Kanoni, Stavroula S; Lagou, Vasiliki V; Li, Rui R; Li, Xin X; Locke, Adam A; Lu, Chen C; Mägi, Reedik R; Perry, John R B JR; Pers, Tune H TH; Qi, Qibin Q; Sanna, Marianna M; Schmidt, Ellen M EM; Scott, William R WR; Shungin, Dmitry D; Teumer, Alexander A; Vinkhuyzen, Anna A E AA; Walker, Ryan W RW; Westra, Harm-Jan HJ; Zhang, Mingfeng M; Zhang, Weihua W; Zhao, Jing Hua JH; Zhu, Zhihong Z; Afzal, Uzma U; Ahluwalia, Tarunveer Singh TS; Bakker, Stephan J L SJ; Bellis, Claire C; Bonnefond, Amélie A; Borodulin, Katja K; Buchman, Aron S AS; Cederholm, Tommy T; Choh, Audrey C AC; Choi, Hyung Jin HJ; Curran, Joanne E JE; de Groot, Lisette C P G M LC; De Jager, Philip L PL; Dhonukshe-Rutten, Rosalie A M RA; Enneman, Anke W AW; Eury, Elodie E; Evans, Daniel S DS; Forsen, Tom T; Friedrich, Nele N; Fumeron, Frédéric F; Garcia, Melissa E ME; Gärtner, Simone S; Han, Bok-Ghee BG; Havulinna, Aki S AS; Hayward, Caroline C; Hernandez, Dena D; Hillege, Hans H; Ittermann, Till T; Kent, Jack W JW; Kolcic, Ivana I; Laatikainen, Tiina T; Lahti, Jari J; Mateo Leach, Irene I; Lee, Christine G CG; Lee, Jong-Young JY; Liu, Tian T; Liu, Youfang Y; Lobbens, Stéphane S; Loh, Marie M; Lyytikäinen, Leo-Pekka LP; Medina-Gomez, Carolina C; Michaëlsson, Karl K; Nalls, Mike A MA; Nielson, Carrie M CM; Oozageer, Laticia L; Pascoe, Laura L; Paternoster, Lavinia L; Polašek, Ozren O; Ripatti, Samuli S; Sarzynski, Mark A MA; Shin, Chan Soo CS; Narančić, Nina Smolej NS; Spira, Dominik D; Srikanth, Priya P; Steinhagen-Thiessen, Elisabeth E; Sung, Yun Ju YJ; Swart, Karin M A KM; Taittonen, Leena L; Tanaka, Toshiko T; Tikkanen, Emmi E; van der Velde, Nathalie N; van Schoor, Natasja M NM; 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Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).
Molecular Psychiatry
Davies, G G; Armstrong, N N; Bis, J C JC; Bressler, J J; Chouraki, V V; Giddaluru, S S; Hofer, E E; Ibrahim-Verbaas, C A CA; Kirin, M M; Lahti, J J; van der Lee, S J SJ; Le Hellard, S S; Liu, T T; Marioni, R E RE; Oldmeadow, C C; Postmus, I I; Smith, A V AV; Smith, J A JA; Thalamuthu, A A; Thomson, R R; Vitart, V V; Wang, J J; Yu, L L; Zgaga, L L; Zhao, W W; Boxall, R R; Harris, S E SE; Hill, W D WD; Liewald, D C DC; Luciano, M M; Adams, H H; Ames, D D; Amin, N N; Amouyel, P P; Assareh, A A AA; Au, R R; Becker, J T JT; Beiser, A A; Berr, C C; Bertram, L L; Boerwinkle, E E; Buckley, B M BM; Campbell, H H; Corley, J J; De Jager, P L PL; Dufouil, C C; Eriksson, J G JG; Espeseth, T T; Faul, J D JD; Ford, I I; , ; Gottesman, R F RF; Griswold, M E ME; Gudnason, V V; Harris, T B TB; Heiss, G G; Hofman, A A; Holliday, E G EG; Huffman, J J; Kardia, S L R SL; Kochan, N N; Knopman, D S DS; Kwok, J B JB; Lambert, J-C JC; Lee, T T; Li, G G; Li, S-C SC; Loitfelder, M M; Lopez, O L OL; Lundervold, A J AJ; Lundqvist, A A; Mather, K A KA; Mirza, S S SS; Nyberg, L L; Oostra, B A BA; Palotie, A A; Papenberg, G G; Pattie, A A; Petrovic, K K; Polasek, O O; Psaty, B M BM; Redmond, P P; Reppermund, S S; Rotter, J I JI; Schmidt, H H; Schuur, M M; Schofield, P W PW; Scott, R J RJ; Steen, V M VM; Stott, D J DJ; van Swieten, J C JC; Taylor, K D KD; Trollor, J J; Trompet, S S; Uitterlinden, A G AG; Weinstein, G G; Widen, E E; Windham, B G BG; Jukema, J W JW; Wright, A F AF; Wright, M J MJ; Yang, Q Q; Amieva, H H; Attia, J R JR; Bennett, D A DA; Brodaty, H H; de Craen, A J M AJ; Hayward, C C; Ikram, M A MA; Lindenberger, U U; Nilsson, L-G LG; Porteous, D J DJ; Räikkönen, K K; Reinvang, I I; Rudan, I I; Sachdev, P S PS; Schmidt, R R; Schofield, P R PR; Srikanth, V V; Starr, J M JM; Turner, S T ST; Weir, D R DR; Wilson, J F JF; van Duijn, C C; Launer, L L; Fitzpatrick, A L AL; Seshadri, S S; Mosley, T H TH; Deary, I J IJ
TOMM40 in Cerebral Amyloid Angiopathy Related Intracerebral Hemorrhage: Comparative Genetic Analysis with Alzheimer's Disease.
Translational Stroke Research
Valant, Valerie V; Keenan, Brendan T BT; Anderson, Christopher D CD; Shulman, Joshua M JM; Devan, William J WJ; Ayres, Alison M AM; Schwab, Kristin K; Goldstein, Joshua N JN; Viswanathan, Anand A; Greenberg, Steven M SM; Bennett, David A DA; De Jager, Philip L PL; Rosand, Jonathan J; Biffi, Alessandro A; ,
Comprehensive search for Alzheimer disease susceptibility loci in the APOE region.
Archives Of Neurology
Jun, Gyungah G; Vardarajan, Badri N BN; Buros, Jacqueline J; Yu, Chang-En CE; Hawk, Michele V MV; Dombroski, Beth A BA; Crane, Paul K PK; Larson, Eric B EB; , ; Mayeux, Richard R; Haines, Jonathan L JL; Lunetta, Kathryn L KL; Pericak-Vance, Margaret A MA; Schellenberg, Gerard D GD; Farrer, Lindsay A LA
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
Nature Genetics
Bis, Joshua C JC; DeCarli, Charles C; Smith, Albert Vernon AV; van der Lijn, Fedde F; Crivello, Fabrice F; Fornage, Myriam M; Debette, Stephanie S; Shulman, Joshua M JM; Schmidt, Helena H; Srikanth, Velandai V; Schuur, Maaike M; Yu, Lei L; Choi, Seung-Hoan SH; Sigurdsson, Sigurdur S; Verhaaren, Benjamin F J BF; DeStefano, Anita L AL; Lambert, Jean-Charles JC; Jack, Clifford R CR; Struchalin, Maksim M; Stankovich, Jim J; Ibrahim-Verbaas, Carla A CA; Fleischman, Debra D; Zijdenbos, Alex A; den Heijer, Tom T; Mazoyer, Bernard B; Coker, Laura H LH; Enzinger, Christian C; Danoy, Patrick P; Amin, Najaf N; Arfanakis, Konstantinos K; van Buchem, Mark A MA; de Bruijn, Renée F A G RF; Beiser, Alexa A; Dufouil, Carole C; Huang, Juebin J; Cavalieri, Margherita M; Thomson, Russell R; Niessen, Wiro J WJ; Chibnik, Lori B LB; Gislason, Gauti K GK; Hofman, Albert A; Pikula, Aleksandra A; Amouyel, Philippe P; Freeman, Kevin B KB; Phan, Thanh G TG; Oostra, Ben A BA; Stein, Jason L JL; Medland, Sarah E SE; Vasquez, Alejandro Arias AA; Hibar, Derrek P DP; Wright, Margaret J MJ; Franke, Barbara B; Martin, Nicholas G NG; Thompson, Paul M PM; , ; Nalls, Michael A MA; Uitterlinden, Andre G AG; Au, Rhoda R; Elbaz, Alexis A; Beare, Richard J RJ; van Swieten, John C JC; Lopez, Oscar L OL; Harris, Tamara B TB; Chouraki, Vincent V; Breteler, Monique M B MM; De Jager, Philip L PL; Becker, James T JT; Vernooij, Meike W MW; Knopman, David D; Fazekas, Franz F; Wolf, Philip A PA; van der Lugt, Aad A; Gudnason, Vilmundur V; Longstreth, W T WT; Brown, Matthew A MA; Bennett, David A DA; van Duijn, Cornelia M CM; Mosley, Thomas H TH; Schmidt, Reinhold R; Tzourio, Christophe C; Launer, Lenore J LJ; Ikram, M Arfan MA; Seshadri, Sudha S; ,
A comprehensive genetic association study of Alzheimer disease in African Americans.
Archives Of Neurology
Logue, Mark W MW; Schu, Matthew M; Vardarajan, Badri N BN; Buros, Jacki J; Green, Robert C RC; Go, Rodney C P RC; Griffith, Patrick P; Obisesan, Thomas O TO; Shatz, Rhonna R; Borenstein, Amy A; Cupples, L Adrienne LA; Lunetta, Kathryn L KL; Fallin, M Daniele MD; Baldwin, Clinton T CT; Farrer, Lindsay A LA; ,
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene.
Plos Genetics
Kapur, Karen K; Johnson, Toby T; Beckmann, Noam D ND; Sehmi, Joban J; Tanaka, Toshiko T; Kutalik, Zoltán Z; Styrkarsdottir, Unnur U; Zhang, Weihua W; Marek, Diana D; Gudbjartsson, Daniel F DF; Milaneschi, Yuri Y; Holm, Hilma H; Diiorio, Angelo A; Waterworth, Dawn D; Li, Yun Y; Singleton, Andrew B AB; Bjornsdottir, Unnur S US; Sigurdsson, Gunnar G; Hernandez, Dena G DG; Desilva, Ranil R; Elliott, Paul P; Eyjolfsson, Gudmundur I GI; Guralnik, Jack M JM; Scott, James J; Thorsteinsdottir, Unnur U; Bandinelli, Stefania S; Chambers, John J; Stefansson, Kari K; Waeber, Gérard G; Ferrucci, Luigi L; Kooner, Jaspal S JS; Mooser, Vincent V; Vollenweider, Peter P; Beckmann, Jacques S JS; Bochud, Murielle M; Bergmann, Sven S
Genome-wide analysis of genetic loci associated with Alzheimer disease.
Jama
Seshadri, Sudha S; Fitzpatrick, Annette L AL; Ikram, M Arfan MA; DeStefano, Anita L AL; Gudnason, Vilmundur V; Boada, Merce M; Bis, Joshua C JC; Smith, Albert V AV; Carassquillo, Minerva M MM; Lambert, Jean Charles JC; Harold, Denise D; Schrijvers, Elisabeth M C EM; Ramirez-Lorca, Reposo R; Debette, Stephanie S; Longstreth, W T WT; Janssens, A Cecile J W AC; Pankratz, V Shane VS; Dartigues, Jean François JF; Hollingworth, Paul P; Aspelund, Thor T; Hernandez, Isabel I; Beiser, Alexa A; Kuller, Lewis H LH; Koudstaal, Peter J PJ; Dickson, Dennis W DW; Tzourio, Christophe C; Abraham, Richard R; Antunez, Carmen C; Du, Yangchun Y; Rotter, Jerome I JI; Aulchenko, Yurii S YS; Harris, Tamara B TB; Petersen, Ronald C RC; Berr, Claudine C; Owen, Michael J MJ; Lopez-Arrieta, Jesus J; Varadarajan, Badri N BN; Becker, James T JT; Rivadeneira, Fernando F; Nalls, Michael A MA; Graff-Radford, Neill R NR; Campion, Dominique D; Auerbach, Sanford S; Rice, Kenneth K; Hofman, Albert A; Jonsson, Palmi V PV; Schmidt, Helena H; Lathrop, Mark M; Mosley, Thomas H TH; Au, Rhoda R; Psaty, Bruce M BM; Uitterlinden, Andre G AG; Farrer, Lindsay A LA; Lumley, Thomas T; Ruiz, Agustin A; Williams, Julie J; Amouyel, Philippe P; Younkin, Steve G SG; Wolf, Philip A PA; Launer, Lenore J LJ; Lopez, Oscar L OL; van Duijn, Cornelia M CM; Breteler, Monique M B MM; , ; , ; ,
Multiple SNPs within and surrounding the apolipoprotein E gene influence cerebrospinal fluid apolipoprotein E protein levels.
Journal Of Alzheimer'S Disease : Jad
Bekris, Lynn M LM; Millard, Steven P SP; Galloway, Nichole M NM; Vuletic, Simona S; Albers, John J JJ; Li, Ge G; Galasko, Douglas R DR; DeCarli, Charles C; Farlow, Martin R MR; Clark, Chris M CM; Quinn, Joseph F JF; Kaye, Jeffrey A JA; Schellenberg, Gerard D GD; Tsuang, Debby D; Peskind, Elaine R ER; Yu, Chang-En CE
Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes.
Bmc Medical Genetics
Kaushal, Ritesh R; Woo, Daniel D; Pal, Prodipto P; Haverbusch, Mary M; Xi, Huifeng H; Moomaw, Charles C; Sekar, Padmini P; Kissela, Brett B; Kleindorfer, Dawn D; Flaherty, Matthew M; Sauerbeck, Laura L; Chakraborty, Ranajit R; Broderick, Joseph J; Deka, Ranjan R
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.
Genomics
Yu, Chang-En CE; Seltman, Howard H; Peskind, Elaine R ER; Galloway, Nichole N; Zhou, Peter X PX; Rosenthal, Elisabeth E; Wijsman, Ellen M EM; Tsuang, Debby W DW; Devlin, Bernie B; Schellenberg, Gerard D GD