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1. Rare coding variants in RCN3 are associated with blood pressure

He, Karen Y.; Kelly, Tanika N.; Wang, Heming; Liang, Jingjing; Zhu, Luke; Cade, Brian E.; Assimes, Themistocles L.; Becker, Lewis C.; Beitelshees, Amber L.; Bielak, Lawrence F.; Bress, Adam P.; Brody, Jennifer A.; Chang, Yen-Pei C.; Chang, Yi-Cheng; de Vries, Paul S.; Duggirala, Ravindranath; Fox, Ervin R.; Franceschini, Nora; Furniss, Anna L.; Gao, Yan; Guo, Xiuqing; Haessler, Jeffrey; Hung, Yi-Jen; Hwang, Shih-Jen; Irvin, Marguerite R.; Kalyani, Rita R.; Liu, Ching-Ti; Liu, Chunyu; Martin, Lisa W.; Montasser, May E.; Muntner, Paul M.; Mwasongwe, Stanford; Naseri, Take; Palmas, Walter; Reupena, Muagututi’a S.; Rice, Kenneth M.; Sheu, Wayne H.; Shimbo, Daichi; Smith, Jennifer A.; Snively, Beverly M.; Yanek, Lisa R.; Zhao, Wei; Blangero, John; Boerwinkle, Eric; Chen, Yii-Der I.; Correa, Adolfo; Cupples, L. A.; Curran, Joanne E.; Fornage, Myriam; He, Jiang; Hou, Lifang; Kaplan, Robert C.; Kardia, Sharon L. R.; Kenny, Eimear E.; Kooperberg, Charles; Lloyd-Jones, Donald; Loos, Ruth J. F.; Mathias, Rasika A.; McGarvey, Stephen T.; Mitchell, Braxton D.; North, Kari E.; Peyser, Patricia A.; Psaty, Bruce M.; Raffield, Laura M.; Rao, D. C.; Redline, Susan; Reiner, Alex P.; Rich, Stephen S.; Rotter, Jerome I.; Taylor, Kent D.; Tracy, Russell; Vasan, Ramachandran S.; Morrison, Alanna C.; Levy, Daniel; Chakravarti, Aravinda; Arnett, Donna K.; Zhu, Xiaofeng
2022
Articles
Human genomeBlood pressureNucleotide sequence

2. Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

Padhi, Evin M.; Hayeck, Tristan J.; Cheng, Zhang; Chatterjee, Sumantra; Mannion, Brandon J.; Byrska-Bishop, Marta; Willems, Marjolaine; Pinson, Lucile; Redon, Sylvia; Benech, Caroline; Uguen, Kevin; Audebert-Bellanger, Séverine; Le Marechal, Cédric; Férec, Claude; Efthymiou, Stephanie; Rahman, Fatima; Maqbool, Shazia; Maroofian, Reza; Houlden, Henry; Musunuri, Rajeeva; Narzisi, Giuseppe; Abhyankar, Avinash; Hunter, Riana D.; Akiyama, Jennifer; Fries, Lauren E.; Ng, Jeffrey K.; Mehinovic, Elvisa; Stong, Nick; Allen, Andrew S.; Dickel, Diane E.; Bernier, Raphael A.; Gorkin, David U.; Pennacchio, Len A.; Zody, Michael C.; Turner, Tychele N.
2021
Articles
AutismHuman genomeNervous system--Diseases--Genetic aspects

4. Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions

Gong, Binsheng; Li, Dan; Kusko, Rebecca; Novoradovskaya, Natalia; Zhang, Yifan; Wang, Shangzi; Pabón-Peña, Carlos; Zhang, Zhihong; Lai, Kevin; Cai, Wanshi; LoCoco, Jennifer S.; Lader, Eric; Richmond, Todd A.; Mittal, Vinay K.; Liu, Liang-Chun; Johann, Donald J.; Willey, James C.; Bushel, Pierre R.; Yu, Ying; Xu, Chang; Chen, Guangchun; Burgess, Daniel; Cawley, Simon; Giorda, Kristina; Haseley, Nathan; Qiu, Fujun; Wilkins, Katherine; Arib, Hanane; Attwooll, Claire; Babson, Kevin; Bao, Longlong; Bao, Wenjun; Lucas, Anne B.; Best, Hunter; Bhandari, Ambica; Bisgin, Halil; Blackburn, James; Blomquist, Thomas M.; Boardman, Lisa; Burgher, Blake; Butler, Daniel J.; Chang, Chia-Jung; Chaubey, Alka; Chen, Tao; Chierici, Marco; Chin, Christopher R.; Close, Devin; Conroy, Jeffrey; Coleman, Jessica C.; Craig, Daniel J.; Crawford, Erin; del Pozo, Angela; Deveson, Ira W.; Duncan, Daniel; Eterovic, Agda K.; Fan, Xiaohui; Foox, Jonathan; Furlanello, Cesare; Ghosal, Abhisek; Glenn, Sean; Guan, Meijian; Haag, Christine; Hang, Xinyi; Happe, Scott; Hennigan, Brittany; Hipp, Jennifer; Hong, Huixiao; Horvath, Kyle; Hu, Jianhong; Hung, Li-Yuan; Jarosz, Mirna; Kerkhof, Jennifer; Kipp, Benjamin; Kreil, David P.; Łabaj, Paweł; Lapunzina, Pablo; Li, Peng; Li, Quan-Zhen; Li, Weihua; Li, Zhiguang; Liang, Yu; Liu, Shaoqing; Liu, Zhichao; Ma, Charles; Marella, Narasimha; Martín-Arenas, Rubén; Megherbi, Dalila B.; Meng, Qingchang; Mieczkowski, Piotr A.; Morrison, Tom; Muzny, Donna; Ning, Baitang; Parsons, Barbara L.; Paweletz, Cloud P.; Pirooznia, Mehdi; Qu, Wubin; Raymond, Amelia; Rindler, Paul; Ringler, Rebecca; Sadikovic, Bekim; Scherer, Andreas; Schulze, Egbert; Sebra, Robert; Shaknovich, Rita; Shi, Qiang; Shi, Tieliu; Silla-Castro, Juan C.; Smith, Melissa; López, Mario S.; Song, Ping; Stetson, Daniel; Strahl, Maya; Stuart, Alan; Supplee, Julianna; Szankasi, Philippe; Tan, Haowen; Tang, Lin-ya; Tao, Yonghui; Thakkar, Shraddha; Thierry-Mieg, Danielle; Thierry-Mieg, Jean; Thodima, Venkat J.; Thomas, David; Tichý, Boris; Tom, Nikola; Garcia, Elena V.; Verma, Suman; Walker, Kimbley; Wang, Charles; Wang, Junwen; Wang, Yexun; Wen, Zhining; Wirta, Valtteri; Wu, Leihong; Xiao, Chunlin; Xiao, Wenzhong; Xu, Shibei; Yang, Mary; Ying, Jianming; Yip, Shun H.; Zhang, Guangliang; Zhang, Sa; Zhao, Meiru; Zheng, Yuanting; Zhou, Xiaoyan; Mason, Christopher E.; Mercer, Timothy; Tong, Weida; Shi, Leming; Jones, Wendell; Xu, Joshua
2021
Articles
Molecular diagnosisCancer--Genetic aspectsHuman genomeBiochemical markersNucleotide sequenceUnited States. Food and Drug Administration

5. Exploiting the GTEx resources to decipher the mechanisms at GWAS loci

Barbeira, Alvaro N.; Bonazzola, Rodrigo; Gamazon, Eric R.; Liang, Yanyu; Park, YoSon; Kim-Hellmuth, Sarah; Wang, Gao; Jiang, Zhuoxun; Zhou, Dan; Hormozdiari, Farhad; Liu, Boxiang; Rao, Abhiram; Hamel, Andrew R.; Pividori, Milton D.; Aguet, François; Jordan, Daniel M.; Verbanck, Marie; Do, Ron; Stephens, Matthew; Ardlie, Kristin; McCarthy, Mark; Montgomery, Stephen B.; Segrè, Ayellet V.; Brown, Christopher D.; Lappalainen, Tuuli; Wen, Xiaoquan; Im, Hae Kyung
2021
Articles
DiseasesHuman genomeGene expressionMedical genetics

9. Whole-genome sequencing data of Kazakh individuals

Kairov, Ulykbek; Molkenov, Askhat; Rakhimova, Saule; Kozhamkulov, Ulan; Sharip, Aigul; Karabayev, Daniyar; Daniyarov, Asset; H.Lee, Joseph; D.Terwilliger, Joseph; Akilzhanova, Ainur; Zhumadilov, Zhaxybay
2021
Articles
Human genomeGenomicsKazakhsPhenotypeBioinformatics

13. Elevated polygenic burden for autism is associated with differential DNA methylation at birth

Hannon, Eilis; Schendel, Diana; Ladd-Acosta, Christine; Grove, Jakob; Hansen, Christine S.; Andrews, Shan V.; Hougaard, David M.; Bresnahan, Michaeline; Mors, Ole; Hollegaard, Mads V.; Bækvad-Hansen, Marie; Hornig, Mady; Mortensen, Preben B.; Børglum, Anders D.; Werge, Thomas; Pedersen, Marianne G.; Nordentoft, Merete; Buxbaum, Joseph; Daniele Fallin, M.; Bybjerg-Grauholm, Jonas; Reichenberg, Abraham; Mill, Jonathan
2018
Articles
DNA--MethylationAutism spectrum disordersGeneticsHuman genome

16. Genome-Wide Association Study of Parity in Bangladeshi Women

Aschebrook-Kilfoy, Briseis; Argos, Maria; Pierce, Brandon L.; Tong, Lin; Jasmine, Farzana; Roy, Shantanu; Parvez, Muhammad F.; Ahmed, Alauddin; Islam, Tariqul; Kibriya, Muhammad G.; Ahsan, Habibul
2015
Articles
Human gene mappingHuman genomeFertility, HumanGeneticsPublic health