Star polymerization of norbornene derivatives using a tri-functionalized Blechert's olefin metathesis catalyst von Zhou, Chulu, Hou, Cuiping, Cheng, Jianhua

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Genome-wide association identifies diverse causes of common variable immunodeficiency von Orange, Jordan S., MD, PhD, Glessner, Joseph T., MS, Resnick, Elena, MD, Sullivan, Kathleen E., MD, Lucas, Mary, MD, Ferry, Berne, MD, Kim, Cecilia E., BS, Hou, Cuiping, BS, Wang, Fengxiang, BS, Chiavacci, Rosetta, BSN, Kugathasan, Subra, MD, Sleasman, John W., MD, Baldassano, Robert, MD, Perez, Elena E., MD, Chapel, Helen, MD, Cunningham-Rundles, Charlotte, MD, Hakonarson, Hakon, MD, PhD

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Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma von Diskin, Sharon J, Capasso, Mario, Schnepp, Robert W, Cole, Kristina A, Attiyeh, Edward F, Hou, Cuiping, Diamond, Maura, Carpenter, Erica L, Winter, Cynthia, Lee, Hanna, Jagannathan, Jayanti, Latorre, Valeria, Iolascon, Achille, Hakonarson, Hakon, Devoto, Marcella, Maris, John M

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Identification of ALK as a major familial neuroblastoma predisposition gene von Mossé, Yaël P., Laudenslager, Marci, Longo, Luca, Cole, Kristina A., Wood, Andrew, Attiyeh, Edward F., Laquaglia, Michael J., Sennett, Rachel, Lynch, Jill E., Perri, Patrizia, Laureys, Geneviève, Speleman, Frank, Kim, Cecilia, Hou, Cuiping, Hakonarson, Hakon, Torkamani, Ali, Schork, Nicholas J., Brodeur, Garrett M., Tonini, Gian P., Rappaport, Eric, Devoto, Marcella, Maris, John M.

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Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma von McDaniel, Lee D, Conkrite, Karina L, Chang, Xiao, Capasso, Mario, Vaksman, Zalman, Oldridge, Derek A, Zachariou, Anna, Horn, Millicent, Diamond, Maura, Hou, Cuiping, Iolascon, Achille, Hakonarson, Hakon, Rahman, Nazneen, Devoto, Marcella, Diskin, Sharon J

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Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations von Li, Yun Rose, Glessner, Joseph T., Coe, Bradley P., Li, Jin, Mohebnasab, Maede, Chang, Xiao, Connolly, John, Kao, Charlly, Wei, Zhi, Bradfield, Jonathan, Kim, Cecilia, Hou, Cuiping, Khan, Munir, Mentch, Frank, Qiu, Haijun, Bakay, Marina, Cardinale, Christopher, Lemma, Maria, Abrams, Debra, Bridglall-Jhingoor, Andrew, Behr, Meckenzie, Harrison, Shanell, Otieno, George, Thomas, Alexandria, Wang, Fengxiang, Chiavacci, Rosetta, Wu, Lawrence, Hadley, Dexter, Goldmuntz, Elizabeth, Elia, Josephine, Maris, John, Grundmeier, Robert, Devoto, Marcella, Keating, Brendan, March, Michael, Pellagrino, Renata, Grant, Struan F. A., Sleiman, Patrick M. A., Li, Mingyao, Eichler, Evan E., Hakonarson, Hakon

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Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms von Diskin, Sharon J, Li, Mingyao, Hou, Cuiping, Yang, Shuzhang, Glessner, Joseph, Hakonarson, Hakon, Bucan, Maja, Maris, John M, Wang, Kai

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Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly von Li, Dong, Wenger, Tara L, Seiler, Christoph, March, Michael E, Gutierrez-Uzquiza, Alvaro, Kao, Charlly, Bhoj, Elizabeth, Tian, Lifeng, Rosenbach, Misha, Liu, Yichuan, Robinson, Nora, Behr, Mechenzie, Chiavacci, Rosetta, Hou, Cuiping, Wang, Tiancheng, Bakay, Marina, Pellegrino da Silva, Renata, Perkins, Jonathan A, Sleiman, Patrick, Levine, Michael A, Hicks, Patricia J, Itkin, Maxim, Dori, Yoav, Hakonarson, Hakon

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Integrative genomics identifies LMO1 as a neuroblastoma oncogene von Wang, Kai, Diskin, Sharon J., Zhang, Haitao, Attiyeh, Edward F., Winter, Cynthia, Hou, Cuiping, Schnepp, Robert W., Diamond, Maura, Bosse, Kristopher, Mayes, Patrick A., Glessner, Joseph, Kim, Cecilia, Frackelton, Edward, Garris, Maria, Wang, Qun, Glaberson, Wendy, Chiavacci, Rosetta, Le Nguyen, Jagannathan, Jayanti, Saeki, Norihisa, Sasaki, Hiroki, Grant, Struan F. A., Iolascon, Achille, Mosse, Yael P., Cole, Kristina A., Li, Hongzhe, Devoto, Marcella, McGrady, Patrick W., London, Wendy B., Capasso, Mario, Rahman, Nazneen, Hakonarson, Hakon, Maris, John M.

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Progress of Application of Ring-Opening Metathesis Polymerization (ROMP) in the Synthesis of Star Polymers von Zhou, Chulu, Hou, Cuiping, Chen, Wei, Wang, Lijie, Cheng, Jianhua

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Carbon Neutrality, International Trade, and Agricultural Carbon Emission Performance in China von Li, Gaoya, Hou, Cuiping, Zhou, Xijun

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Copy number variation at 1q21.1 associated with neuroblastoma von Diskin, Sharon J., Hou, Cuiping, Glessner, Joseph T., Attiyeh, Edward F., Laudenslager, Marci, Bosse, Kristopher, Cole, Kristina, Mossé, Yaël P., Wood, Andrew, Lynch, Jill E., Pecor, Katlyn, Diamond, Maura, Winter, Cynthia, Wang, Kai, Kim, Cecilia, Geiger, Elizabeth A., McGrady, Patrick W., Blakemore, Alexandra I. F., London, Wendy B., Shaikh, Tamim H., Bradfield, Jonathan, Grant, Struan F. A., Li, Hongzhe, Devoto, Marcella, Rappaport, Eric R., Hakonarson, Hakon, Maris, John M.

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No Significant Association of 14 Candidate Genes With Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics von Sanders, Alan R., Duan, Jubao, Levinson, Douglas F., Shi, Jianxin, He, Deli, Hou, Cuiping, Burrell, Gregory J., Rice, John P., Nertney, Deborah A., Olincy, Ann, Rozic, Pablo, Vinogradov, Sophia, Buccola, Nancy G., Mowry, Bryan J., Freedman, Robert, Amin, Farooq, Black, Donald W., Silverman, Jeremy M., Byerley, William F., Crowe, Raymond R., Cloninger, C. Robert, Martinez, Maria, Gejman, Pablo V.

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Common variations in BARD1 influence susceptibility to high-risk neuroblastoma von Devoto, Marcella, Hakonarson, Hakon, Maris, John M, Capasso, Mario, Hou, Cuiping, Asgharzadeh, Shahab, Glessner, Joseph T, Attiyeh, Edward F, Mosse, Yael P, Kim, Cecilia, Diskin, Sharon J, Cole, Kristina A, Bosse, Kristopher, Diamond, Maura, Laudenslager, Marci, Winter, Cynthia, Bradfield, Jonathan P, Scott, Richard H, Jagannathan, Jayanti, Garris, Maria, McConville, Carmel, London, Wendy B, Seeger, Robert C, Grant, Struan F A, Li, Hongzhe, Rahman, Nazneen, Rappaport, Eric

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Variants of DENND1B Associated with Asthma in Children von Sleiman, Patrick M.A, Flory, James, Imielinski, Marcin, Bradfield, Jonathan P, Annaiah, Kiran, Willis-Owen, Saffron A.G, Wang, Kai, Rafaels, Nicholas M, Michel, Sven, Bonnelykke, Klaus, Zhang, Haitao, Kim, Cecilia E, Frackelton, Edward C, Glessner, Joseph T, Hou, Cuiping, Otieno, F. George, Santa, Erin, Thomas, Kelly, Smith, Ryan M, Glaberson, Wendy R, Garris, Maria, Chiavacci, Rosetta M, Beaty, Terri H, Ruczinski, Ingo, Orange, Jordan M, Allen, Julian, Spergel, Jonathan M, Grundmeier, Robert, Mathias, Rasika A, Christie, Jason D, von Mutius, Erika, Cookson, William O.C, Kabesch, Michael, Moffatt, Miriam F, Grunstein, Michael M, Barnes, Kathleen C, Devoto, Marcella, Magnusson, Mark, Li, Hongzhe, Grant, Struan F.A, Bisgaard, Hans, Hakonarson, Hakon

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Diverse Genome-wide Association Studies Associate the IL12/IL23 Pathway with Crohn Disease von Wang, Kai, Zhang, Haitao, Kugathasan, Subra, Annese, Vito, Bradfield, Jonathan P., Russell, Richard K., Sleiman, Patrick M.A., Imielinski, Marcin, Glessner, Joseph, Hou, Cuiping, Wilson, David C., Walters, Thomas, Kim, Cecilia, Frackelton, Edward C., Lionetti, Paolo, Barabino, Arrigo, Van Limbergen, Johan, Guthery, Stephen, Denson, Lee, Piccoli, David, Li, Mingyao, Dubinsky, Marla, Silverberg, Mark, Griffiths, Anne, Grant, Struan F.A., Satsangi, Jack, Baldassano, Robert, Hakonarson, Hakon

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Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder von Keller, Michael D., MD, Pandey, Rahul, PhD, Li, Dong, PhD, Glessner, Joseph, PhD, Tian, Lifeng, PhD, Henrickson, Sarah E., MD, PhD, Chinn, Ivan K., MD, Monaco-Shawver, Linda, BSc, Heimall, Jennifer, MD, Hou, Cuiping, BSc, Otieno, Frederick G., MS, Jyonouchi, Soma, MD, Calabrese, Leonard, DO, van Montfrans, Joris, MD, Orange, Jordan S., MD, PhD, Hakonarson, Hakon, MD, PhD

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From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes von Wei, Zhi, Wang, Kai, Qu, Hui-Qi, Zhang, Haitao, Bradfield, Jonathan, Kim, Cecilia, Frackleton, Edward, Hou, Cuiping, Glessner, Joseph T, Chiavacci, Rosetta, Stanley, Charles, Monos, Dimitri, Grant, Struan F A, Polychronakos, Constantin, Hakonarson, Hakon

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Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma von Maris, John M, Mosse, Yael P, Bradfield, Jonathan P, Hou, Cuiping, Monni, Stefano, Scott, Richard H, Asgharzadeh, Shahab, Attiyeh, Edward F, Diskin, Sharon J, Laudenslager, Marci, Winter, Cynthia, Cole, Kristina A, Glessner, Joseph T, Kim, Cecilia, Frackelton, Edward C, Casalunovo, Tracy, Eckert, Andrew W, Capasso, Mario, Rappaport, Eric F, McConville, Carmel, London, Wendy B, Seeger, Robert C, Rahman, Nazneen, Devoto, Marcella, Grant, Struan F.A, Li, Hongzhe, Hakonarson, Hakon

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Common Variation at BARD1 Results in the Expression of an Oncogenic Isoform That Influences Neuroblastoma Susceptibility and Oncogenicity von BOSSE, Kristopher R, DISKIN, Sharon J, DIAMOND, Maura, CUIPING HOU, ATTIYEH, Edward F, MOSSE, Yael P, PINEROS, Vanessa, DIZIN, Eva, YONGQIANG ZHANG, ASGHARZADEH, Shahab, SEEGER, Robert C, CAPASSO, Mario, COLE, Kristina A, PAWEL, Bruce R, DEVOTO, Marcella, HAKONARSON, Hakon, RAPPAPORT, Eric F, IRMINGER-FINGER, Irmgard, MARIA, John M, WOOD, Andrew C, SCHNEPP, Robert W, NORRIS, Geoffrey, NGUYEN, Le B, JAGANNATHAN, Jayanti, LAQUAGLIA, Michael, WINTER, Cynthia

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