Genetics and Genomics of Congenital Heart Disease von Zaidi, Samir, Brueckner, Martina

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Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles von Timberlake, Andrew T, Choi, Jungmin, Zaidi, Samir, Lu, Qiongshi, Nelson-Williams, Carol, Brooks, Eric D, Bilguvar, Kaya, Tikhonova, Irina, Mane, Shrikant, Yang, Jenny F, Sawh-Martinez, Rajendra, Persing, Sarah, Zellner, Elizabeth G, Loring, Erin, Chuang, Carolyn, Galm, Amy, Hashim, Peter W, Steinbacher, Derek M, DiLuna, Michael L, Duncan, Charles C, Pelphrey, Kevin A, Zhao, Hongyu, Persing, John A, Lifton, Richard P

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Brain atlas for glycoprotein hormone receptors at single-transcript level von Ryu, Vitaly, Gumerova, Anisa, Korkmaz, Funda, Kang, Seong Su, Katsel, Pavel, Miyashita, Sari, Kannangara, Hasni, Cullen, Liam, Chan, Pokman, Kuo, TanChun, Padilla, Ashley, Sultana, Farhath, Wizman, Soleil A, Kramskiy, Natan, Zaidi, Samir, Kim, Se-Min, New, Maria I, Rosen, Clifford J, Goosens, Ki A, Frolinger, Tal, Haroutunian, Vahram, Ye, Keqiang, Lizneva, Daria, Davies, Terry F, Yuen, Tony, Zaidi, Mone

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Anabolic actions of Notch on mature bone von Liu, Peng, Ping, Yilin, Ma, Meng, Zhang, Demao, Liu, Connie, Zaidi, Samir, Gao, Song, Ji, Yaoting, Lou, Feng, Yu, Fanyuan, Lu, Ping, Stachnik, Agnes, Bai, Mingru, Wei, Chengguo, Zhang, Liaoran, Wang, Ke, Chen, Rong, New, Maria I., Rowe, David W., Yuen, Tony, Sun, Li, Zaidi, Mone

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Loss of RNA expression and allele-specific expression associated with congenital heart disease von McKean, David M., Homsy, Jason, Wakimoto, Hiroko, Patel, Neil, Gorham, Joshua, DePalma, Steven R., Ware, James S., Zaidi, Samir, Ma, Wenji, Patel, Nihir, Lifton, Richard P., Chung, Wendy K., Kim, Richard, Shen, Yufeng, Brueckner, Martina, Goldmuntz, Elizabeth, Sharp, Andrew J., Seidman, Christine E., Gelb, Bruce D., Seidman, J. G.

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Understanding osteokine biology von Zaidi, Mone, Zaidi, Samir, Yuen, Tony

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Neurogenetic analysis of childhood disintegrative disorder von Gupta, Abha R, Westphal, Alexander, Yang, Daniel Y J, Sullivan, Catherine A W, Eilbott, Jeffrey, Zaidi, Samir, Voos, Avery, Vander Wyk, Brent C, Ventola, Pam, Waqar, Zainulabedin, Fernandez, Thomas V, Ercan-Sencicek, A Gulhan, Walker, Michael F, Choi, Murim, Schneider, Allison, Hedderly, Tammy, Baird, Gillian, Friedman, Hannah, Cordeaux, Cara, Ristow, Alexandra, Shic, Frederick, Volkmar, Fred R, Pelphrey, Kevin A

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Congenital heart disease: emerging themes linking genetics and development von Yuan, Shiaulou, Zaidi, Samir, Brueckner, Martina

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Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening von Stuart, Bridget D, Choi, Jungmin, Zaidi, Samir, Xing, Chao, Holohan, Brody, Chen, Rui, Choi, Mihwa, Dharwadkar, Pooja, Torres, Fernando, Girod, Carlos E, Weissler, Jonathan, Fitzgerald, John, Kershaw, Corey, Klesney-Tait, Julia, Mageto, Yolanda, Shay, Jerry W, Ji, Weizhen, Bilguvar, Kaya, Mane, Shrikant, Lifton, Richard P, Garcia, Christine Kim

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Lineage plasticity in prostate cancer depends on JAK/STAT inflammatory signaling von Chan, Joseph M, Zaidi, Samir, Love, Jillian R, Zhao, Jimmy L, Setty, Manu, Wadosky, Kristine M, Gopalan, Anuradha, Choo, Zi-Ning, Persad, Sitara, Choi, Jungmin, LaClair, Justin, Lawrence, Kayla E, Chaudhary, Ojasvi, Xu, Tianhao, Masilionis, Ignas, Linkov, Irina, Wang, Shangqian, Lee, Cindy, Barlas, Afsar, Morris, Michael J, Mazutis, Linas, Chaligne, Ronan, Chen, Yu, Goodrich, David W, Karthaus, Wouter R, Pe'er, Dana, Sawyers, Charles L

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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands von Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R, Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C, Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D, Castaldi, Christopher, Tikhonoa, Irina R, Bilguvar, Kaya, Mane, Shrikant M, Sanders, Stephan J, Mital, Seema, Russell, Mark W, Gaynor, J William, Deanfield, John, Giardini, Alessandro, Porter, George A, Srivastava, Deepak, Lo, Cecelia W, Shen, Yufeng, Watkins, W Scott, Yandell, Mark, Yost, H Joseph, Tristani-Firouzi, Martin, Newburger, Jane W, Roberts, Amy E, Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R, Goldmuntz, Elizabeth, Chung, Wendy K, Seidman, Jonathan G, Gelb, Bruce D, Seidman, Christine E, Lifton, Richard P, Brueckner, Martina

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De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies von Homsy, Jason, Zaidi, Samir, Shen, Yufeng, Ware, James S., Samocha, Kaitlin E., Karczewski, Konrad J., DePalma, Steven R., McKean, David, Wakimoto, Hiroko, Gorham, Josh, Jin, Sheng Chih, Deanfield, John, Giardini, Alessandro, Porter, George A., Kim, Richard, Bilguvar, Kaya, López-Giráldez, Francesc, Tikhonova, Irina, Mane, Shrikant, Romano-Adesman, Angela, Qi, Hongjian, Vardarajan, Badri, Ma, Lijiang, Daly, Mark, Roberts, Amy E., Russell, Mark W., Mital, Seema, Newburger, Jane W., Gaynor, J. William, Breitbart, Roger E., Iossifov, Ivan, Ronemus, Michael, Sanders, Stephan J., Kaltman, Jonathan R., Seidman, Jonathan G., Brueckner, Martina, Gelb, Bruce D., Goldmuntz, Elizabeth, Lifton, Richard P., Seidman, Christine E., Chung, Wendy K.

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Genomic alterations and evolution in patients with prostate cancer with histologic evidence of neuroendocrine differentiation von Barnett, Ethan, Carbone, Emily, Keegan, Niamh M., Vasselman, Samantha E, Nweji, Barbara, Zaidi, Samir, Scher, Howard I.

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Oct4 expression is not required for mouse somatic stem cell self-renewal von Lengner, Christopher J, Camargo, Fernando D, Hochedlinger, Konrad, Welstead, G Grant, Zaidi, Samir, Gokhale, Sumita, Scholer, Hans R, Tomilin, Alexey, Jaenisch, Rudolf

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Integrated mutational landscape analysis of uterine leiomyosarcomas von Choi, Jungmin, Manzano, Aranzazu, Dong, Weilai, Bellone, Stefania, Bonazzoli, Elena, Zammataro, Luca, Yao, Xiaotong, Deshpande, Aditya, Zaidi, Samir, Guglielmi, Adele, Gnutti, Barbara, Nagarkatti, Nupur, Tymon-Rosario, Joan R., Harold, Justin, Mauricio, Dennis, Zeybek, Burak, Menderes, Gulden, Altwerger, Gary, Jeong, Kyungjo, Zhao, Siming, Buza, Natalia, Hui, Pei, Ravaggi, Antonella, Bignotti, Eliana, Romani, Chiara, Todeschini, Paola, Zanotti, Laura, Odicino, Franco, Pecorelli, Sergio, Ardighieri, Laura, Bilguvar, Kaya, Quick, Charles M., Silasi, Dan-Arin, Huang, Gloria S., Andikyan, Vaagn, Clark, Mitchell, Ratner, Elena, Azodi, Masoud, Imielinski, Marcin, Schwartz, Peter E., Alexandrov, Ludmil B., Lifton, Richard P., Schlessinger, Joseph, Santin, Alessandro D.

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FSH Directly Regulates Bone Mass von Sun, Li, Peng, Yuanzhen, Sharrow, Allison C., Iqbal, Jameel, Zhang, Zhiyuan, Papachristou, Dionysios J., Zaidi, Samir, Zhu, Ling-Ling, Yaroslavskiy, Beatrice B., Zhou, Hang, Zallone, Alberta, Sairam, M. Ram, Kumar, T. Rajendra, Bo, Wei, Braun, Jonathan, Cardoso-Landa, Luis, Schaffler, Mitchell B., Moonga, Baljit S., Blair, Harry C., Zaidi, Mone

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Effect of Janus kinase (JAK) signaling inhibition on lineage plasticity and drug sensitivity in castrate resistant prostate cancer von Zaidi, Samir, Chan, Joseph Minhow, Love, Jillian, Zhao, Jimmy, Setty, Manu, Lawrence, Kayla, Gopalan, Anuradha, Goodrich, David, Morris, Michael J., Chen, Yu, Karthaus, Wouter, Pe'er, Dana, Sawyers, Charles L.

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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency von Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Badi, Maryam Al, Alzubdi, Mouch, Wilson, Robert C., Azkawi, Hanan Said Al, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W., Senani, Aisha Al, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I.

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A phase 2 evaluation of pembrolizumab for recurrent Lynch‐like versus sporadic endometrial cancers with microsatellite instability von Bellone, Stefania, Roque, Dana M., Siegel, Eric R., Buza, Natalia, Hui, Pei, Bonazzoli, Elena, Guglielmi, Adele, Zammataro, Luca, Nagarkatti, Nupur, Zaidi, Samir, Lee, Jungsoo, Silasi, Dan‐Arin, Huang, Gloria S., Andikyan, Vaagn, Damast, Shari, Clark, Mitchell, Azodi, Masoud, Schwartz, Peter E., Tymon‐Rosario, Joan R., Harold, Justin A., Mauricio, Dennis, Zeybek, Burak, Menderes, Gulden, Altwerger, Gary, Ratner, Elena, Alexandrov, Ludmil B., Iwasaki, Akiko, Kong, Yong, Song, Eric, Dong, Weilai, Elvin, Julia A., Choi, Jungmin, Santin, Alessandro D.

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Histone H2B monoubiquitination regulates heart development via epigenetic control of cilia motility von Robson, Andrew, Makova, Svetlana Z., Barish, Syndi, Zaidi, Samir, Mehta, Sameet, Drozd, Jeffrey, Jin, Sheng Chih, Gelb, Bruce D., Seidman, Christine E., Chung, Wendy K., Lifton, Richard P., Khokha, Mustafa K., Brueckner, Martina

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