SparkText: Biomedical Text Mining on Big Data Framework von Ye, Zhan, Tafti, Ahmad P, He, Karen Y, Wang, Kai, He, Max M

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Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants von He, Max M, Li, Quan, Yan, Muqing, Cao, Hui, Hu, Yue, He, Karen Y, Cao, Kajia, Li, Marilyn M, Wang, Kai

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Multivariate Analysis of Anthropometric Traits Using Summary Statistics of Genome-Wide Association Studies from GIANT Consortium von Park, Haeil, Li, Xiaoyin, Song, Yeunjoo E, He, Karen Y, Zhu, Xiaofeng

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Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants von He, Karen Y., Khramtsova, Ekaterina A., Cabrera-Socorro, Alfredo, Zhang, Yanfei, Li, Shuwei, Sarver, Brice A. J., Smets, Bart, Li, Qingqin S., De Muynck, Louis, Parrado, Antonio R., Lovestone, Simon, Black, Mary Helen

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Detecting fitness epistasis in recently admixed populations with genome-wide data von Ni, Xumin, Zhou, Mengshi, Wang, Heming, He, Karen Y, Broeckel, Uli, Hanis, Craig, Kardia, Sharon, Redline, Susan, Cooper, Richard S, Tang, Hua, Zhu, Xiaofeng

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Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure von He, Karen Y, Wang, Heming, Cade, Brian E, Nandakumar, Priyanka, Giri, Ayush, Ware, Erin B, Haessler, Jeffrey, Liang, Jingjing, Smith, Jennifer A, Franceschini, Nora, Le, Thu H, Kooperberg, Charles, Edwards, Todd L, Kardia, Sharon L R, Lin, Xihong, Chakravarti, Aravinda, Redline, Susan, Zhu, Xiaofeng

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Big Data Analytics for Genomic Medicine von He, Karen Y, Ge, Dongliang, He, Max M

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Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records von He, Karen Y, Zhao, Yiqing, McPherson, Elizabeth W, Li, Quan, Xia, Fan, Weng, Chunhua, Wang, Kai, He, Max M

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Quality control and analytic best practices for testing genetic models of sex differences in large populations von Khramtsova, Ekaterina A., Wilson, Melissa A., Martin, Joanna, Winham, Stacey J., He, Karen Y., Davis, Lea K., Stranger, Barbara E.

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Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea von Liang, Jingjing, Wang, Heming, Cade, Brian E, Kurniansyah, Nuzulul, He, Karen Y, Lee, Jiwon, Sands, Scott A, A Brody, Jennifer, Chen, Han, Gottlieb, Daniel J, Evans, Daniel S, Guo, Xiuqing, Gharib, Sina A, Hale, Lauren, Hillman, David R, Lutsey, Pamela L, Mukherjee, Sutapa, Ochs-Balcom, Heather M, Palmer, Lyle J, Purcell, Shaun, Saxena, Richa, Patel, Sanjay R, Stone, Katie L, Tranah, Gregory J, Boerwinkle, Eric, Lin, Xihong, Liu, Yongmei, Psaty, Bruce M, Vasan, Ramachandran S, Manichaikul, Ani, Rich, Stephen S, Rotter, Jerome I, Sofer, Tamar, Redline, Susan, Zhu, Xiaofeng

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Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension von Kelly, Tanika N., Sun, Xiao, He, Karen Y., Brown, Michael R., Taliun, Sarah A. Gagliano, Hellwege, Jacklyn N., Irvin, Marguerite R., Mi, Xuenan, Brody, Jennifer A., Franceschini, Nora, Guo, Xiuqing, Hwang, Shih-Jen, de Vries, Paul S., Gao, Yan, Moscati, Arden, Nadkarni, Girish N., Yanek, Lisa R., Elfassy, Tali, Smith, Jennifer A., Chung, Ren-Hua, Beitelshees, Amber L., Patki, Amit, Aslibekyan, Stella, Blobner, Brandon M., Peralta, Juan M., Assimes, Themistocles L., Palmas, Walter R., Liu, Chunyu, Bress, Adam P., Huang, Zhijie, Hwa, Chii-Min, O’Connell, Jeffrey R., Carlson, Jenna C., Warren, Helen R., Das, Sayantan, Giri, Ayush, Martin, Lisa W., Craig Johnson, W., Fox, Ervin R., Bottinger, Erwin P., Razavi, Alexander C., Vaidya, Dhananjay, Chuang, Lee-Ming, Chang, Yen-Pei C., Jain, Deepti, Kang, Hyun Min, Hung, Adriana M., Srinivasasainagendra, Vinodh, Snively, Beverly M., Gu, Dongfeng, Montasser, May E., Reupena, Muagututi‘a Sefuiva, Heavner, Benjamin D., LeFaive, Jonathon, Hixson, James E., Rice, Kenneth M., Wang, Fei Fei, Nielsen, Jonas B., Huang, Jianfeng, Khan, Alyna T., Zhou, Wei, Nierenberg, Jovia L., Laurie, Cathy C., Armstrong, Nicole D., Shi, Mengyao, Pan, Yang, Stilp, Adrienne M., Emery, Leslie, Wong, Quenna, Minster, Ryan L., Curran, Joanne E., Munroe, Patricia B., Weeks, Daniel E., North, Kari E., Tracy, Russell P., Kenny, Eimear E., Shimbo, Daichi, Chakravarti, Aravinda, Rich, Stephen S., Blangero, John, Redline, Susan, Mitchell, Braxton D., Ida Chen, Yii-Der, Kardia, Sharon L.R., Kaplan, Robert C., Mathias, Rasika A., He, Jiang, Psaty, Bruce M., Fornage, Myriam, Loos, Ruth J.F., Correa, Adolfo, Boerwinkle, Eric, Rotter, Jerome I., Kooperberg, Charles, Edwards, Todd L., Abecasis, Gonçalo R., Zhu, Xiaofeng, Levy, Daniel, Arnett, Donna K., Morrison, Alanna C.

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Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level von Liang, Jingjing, Cade, Brian E., He, Karen Y., Wang, Heming, Lee, Jiwon, Sofer, Tamar, Williams, Stephanie, Li, Ruitong, Chen, Han, Gottlieb, Daniel J., Evans, Daniel S., Guo, Xiuqing, Gharib, Sina A., Hale, Lauren, Hillman, David R., Lutsey, Pamela L., Mukherjee, Sutapa, Ochs-Balcom, Heather M., Palmer, Lyle J., Rhodes, Jessica, Purcell, Shaun, Patel, Sanjay R., Saxena, Richa, Stone, Katie L., Tang, Weihong, Tranah, Gregory J., Boerwinkle, Eric, Lin, Xihong, Liu, Yongmei, Psaty, Bruce M., Vasan, Ramachandran S., Cho, Michael H., Manichaikul, Ani, Silverman, Edwin K., Barr, R. Graham, Rich, Stephen S., Rotter, Jerome I., Wilson, James G., Redline, Susan, Zhu, Xiaofeng

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Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data von He, Karen Y., Li, Xiaoyin, Kelly, Tanika N., Liang, Jingjing, Cade, Brian E., Assimes, Themistocles L., Becker, Lewis C., Beitelshees, Amber L., Bress, Adam P., Chang, Yen-Pei Christy, Chen, Yii-Der Ida, de Vries, Paul S., Fox, Ervin R., Franceschini, Nora, Furniss, Anna, Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hwang, Shih-Jen, Irvin, Marguerite Ryan, Kalyani, Rita R., Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E., Muntner, Paul M., Mwasongwe, Stanford, Palmas, Walter, Reiner, Alex P., Shimbo, Daichi, Smith, Jennifer A., Snively, Beverly M., Yanek, Lisa R., Boerwinkle, Eric, Correa, Adolfo, Cupples, L. Adrienne, He, Jiang, Kardia, Sharon L. R., Kooperberg, Charles, Mathias, Rasika A., Mitchell, Braxton D., Psaty, Bruce M., Vasan, Ramachandran S., Rao, D. C., Rich, Stephen S., Rotter, Jerome I., Wilson, James G., Chakravarti, Aravinda, Morrison, Alanna C., Levy, Daniel, Arnett, Donna K., Redline, Susan, Zhu, Xiaofeng

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Rare coding variants in RCN3 are associated with blood pressure von 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 Christy, 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 Ryan, Kalyani, Rita R, Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E, Muntner, Paul M, Mwasongwe, Stanford, Naseri, Take, Palmas, Walter, Reupena, Muagututi'a Sefuiva, Rice, Kenneth M, Sheu, Wayne H-H, Shimbo, Daichi, Smith, Jennifer A, Snively, Beverly M, Yanek, Lisa R, Zhao, Wei, Blangero, John, Boerwinkle, Eric, Chen, Yii-Der Ida, Correa, Adolfo, Cupples, L Adrienne, 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

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Abstract 46: Whole Genome Sequence Analysis Of Blood Pressure Phenotypes In The Trans-omics For Precision Medicine And Centers For Common Disease Genomics Programs von Kelly, Tanika N, Sun, Xiao, Brody, Jennifer A, Gagliano, Sarah A, He, Karen Y, Hellwege, Jacklyn N

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Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension von Sun, Xiao, He, Karen Y., Brown, Michael R., Taliun, Sarah A. Gagliano, Hellwege, Jacklyn N., Irvin, Marguerite R., Mi, Xuenan, Brody, Jennifer A., Franceschini, Nora, Guo, Xiuqing, Hwang, Shih-Jen, de Vries, Paul S., Gao, Yan, Moscati, Arden, Nadkarni, Girish N., Yanek, Lisa R., Elfassy, Tali, Smith, Jennifer A., Chung, Ren-Hua, Beitelshees, Amber L., Patki, Amit, Aslibekyan, Stella, Blobner, Brandon M., Peralta, Juan M., Assimes, Themistocles L., Palmas, Walter R., Liu, Chunyu, Bress, Adam P., Huang, Zhijie, Becker, Lewis C., Hwa, Chii-Min, O’Connell, Jeffrey R., Carlson, Jenna C., Warren, Helen R., Das, Sayantan, Martin, Lisa W., Craig Johnson, W., Fox, Ervin R., Bottinger, Erwin P., Razavi, Alexander C., Vaidya, Dhananjay, Chuang, Lee-Ming, Chang, Yen-Pei C., Naseri, Take, Jain, Deepti, Kang, Hyun Min, Hung, Adriana M., Srinivasasainagendra, Vinodh, Snively, Beverly M., Gu, Dongfeng, Montasser, May E., Reupena, Muagututi‘a Sefuiva, Heavner, Benjamin D., Hixson, James E., Rice, Kenneth M., Wang, Fei Fei, Nielsen, Jonas B., Huang, Jianfeng, Khan, Alyna T., Zhou, Wei, Nierenberg, Jovia L., Laurie, Cathy C., Armstrong, Nicole D., Shi, Mengyao, Pan, Yang, Stilp, Adrienne M., Emery, Leslie, Wong, Quenna, Hawley, Nicola L., Minster, Ryan L., Curran, Joanne E., Munroe, Patricia B., Weeks, Daniel E., North, Kari E., Tracy, Russell P., Kenny, Eimear E., Shimbo, Daichi, Chakravarti, Aravinda, Rich, Stephen S., Reiner, Alex P., Blangero, John, Redline, Susan, Mitchell, Braxton D., Ida Chen, Yii-Der, Kardia, Sharon L.R., Kaplan, Robert C., Mathias, Rasika A., He, Jiang, Psaty, Bruce M., Fornage, Myriam, Loos, Ruth J.F., Correa, Adolfo, Boerwinkle, Eric, Rotter, Jerome I., Kooperberg, Charles, Edwards, Todd L., Abecasis, Gonçalo R., Zhu, Xiaofeng, Levy, Daniel, Arnett, Donna K.

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Rare variants in fox-1 homolog A von Lin, Xihong, Zhu, Xiaofeng, Edwards, Todd L, Redline, Susan, Nandakumar, Priyanka, Smith, Jennifer A, Ware, Erin B, Haessler, Jeffrey, Wang, Heming, Kardia, Sharon L. R, Cade, Brian E, Le, Thu H, He, Karen Y, Franceschini, Nora, Chakravarti, Aravinda, Liang, Jingjing, Giri, Ayush, Kooperberg, Charles

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Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants von He, Karen Y, Khramtsova, Ekaterina A, Cabrera-Socorro, Alfredo, Zhang, Yanfei, Li, Shuwei, Sarver, Brice A. J, Smets, Bart, Li, Qingqin S, De Muynck, Louis, Parrado, Antonio R, Lovestone, Simon, Black, Mary Helen

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Detecting fitness epistasis in recently admixed populations with genome-wide data von Ni, Xumin, Zhou, Mengshi, Wang, Heming, He, Karen Y, Broeckel, Uli, Hanis, Craig, Kardia, Sharon, Redline, Susan, Cooper, Richard S, Tang, Hua, Zhu, Xiaofeng

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Detecting fitness epistasis in recently admixed populations with genome-wide data von Ni, Xumin, Zhou, Mengshi, Wang, Heming, He, Karen Y, Broeckel, Uli, Hanis, Craig, Kardia, Sharon, Redline, Susan, Cooper, Richard S, Tang, Hua, Zhu, Xiaofeng

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