Francis H. Ruddle (1929-2013): A Pioneer in Human Gene Mapping von Kucherlapati, Raju

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Impaired lymphatic contraction associated with immunosuppression von Liao, Shan, Cheng, Gang, Conner, David A., Huang, Yuhui, Kucherlapati, Raju S., Munn, Lance L., Ruddle, Nancy H., Jain, Rakesh K., Fukumura, Dai, Padera, Timothy P.

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Landscape of Somatic Retrotransposition in Human Cancers von Lee, Eunjung, Iskow, Rebecca, Yang, Lixing, Gokcumen, Omer, Haseley, Psalm, Luquette, Lovelace J., Lohr, Jens G., Harris, Christopher C., Ding, Li, Wilson, Richard K., Wheeler, David A., Gibbs, Richard A., Kucherlapati, Raju, Lee, Charles, Kharchenko, Peter V., Park, Peter J.

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Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes von Yang, Lixing, Luquette, Lovelace J., Gehlenborg, Nils, Xi, Ruibin, Haseley, Psalm S., Hsieh, Chih-Heng, Zhang, Chengsheng, Ren, Xiaojia, Protopopov, Alexei, Chin, Lynda, Kucherlapati, Raju, Lee, Charles, Park, Peter J.

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Clinical significance of CTNNB1 mutation and Wnt pathway activation in endometrioid endometrial carcinoma von Liu, Yuexin, Patel, Lalit, Mills, Gordon B, Lu, Karen H, Sood, Anil K, Ding, Li, Kucherlapati, Raju, Mardis, Elaine R, Levine, Douglas A, Shmulevich, Ilya, Broaddus, Russell R, Zhang, Wei

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Germline gain-of-function mutations in SOS1 cause Noonan syndrome von Neel, Benjamin G, Roberts, Amy E, Araki, Toshiyuki, Swanson, Kenneth D, Montgomery, Kate T, Schiripo, Taryn A, Joshi, Victoria A, Li, Li, Yassin, Yosuf, Tamburino, Alex M, Kucherlapati, Raju S

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Genetically Modified Mouse Models for Biomarker Discovery and Preclinical Drug Testing von KUCHERLAPATI, Raju

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Cardiovascular disease in Noonan syndrome von Prendiville, Terence W, Gauvreau, Kimberlee, Tworog-Dube, Erica, Patkin, Lynne, Kucherlapati, Raju S, Roberts, Amy E, Lacro, Ronald V

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A restricted spectrum of NRAS mutations causes Noonan syndrome von Gelb, Bruce D, Gremer, Lothar, Digilio, Cristina, Dentici, Maria L, Roberts, Amy E, Zampino, Giuseppe, Kratz, Christian P, Dallapiccola, Bruno, Mazzanti, Laura, Stuppia, Liborio, Pantaleoni, Francesca, Ahmadian, Mohammad R, Zenker, Martin, Lepri, Francesca, Kutsche, Kerstin, Silengo, Margherita Cirillo, Joshi, Victoria A, König, Rainer, Carta, Claudio, Horn, Denise, Merbitz-Zahradnik, Torsten, Pennacchio, Len A, Mundlos, Stefan, Tartaglia, Marco, Dvorsky, Radovan, Wittinghofer, Alfred, Cirstea, Ion C, Seemanova, Eva, Patton, Michael A, Rossi, Cesare, Kucherlapati, Raju S

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Global impact of somatic structural variation on the DNA methylome of human cancers von Zhang, Yiqun, Yang, Lixing, Kucherlapati, Melanie, Hadjipanayis, Angela, Pantazi, Angeliki, Bristow, Christopher A, Lee, Eunjung Alice, Mahadeshwar, Harshad S, Tang, Jiabin, Zhang, Jianhua, Seth, Sahil, Lee, Semin, Ren, Xiaojia, Song, Xingzhi, Sun, Huandong, Seidman, Jonathan, Luquette, Lovelace J, Xi, Ruibin, Chin, Lynda, Protopopov, Alexei, Park, Peter J, Kucherlapati, Raju, Creighton, Chad J

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Spectrum of somatic mitochondrial mutations in five cancers von Larman, Tatianna C, DePalma, Steven R, Hadjipanayis, Angela G, Protopopov, Alexei, Zhang, Jianhua, Gabriel, Stacey B, Chin, Lynda, Seidman, Christine E, Kucherlapati, Raju, Seidman, J. G

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A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases von Zhang, Yiqun, Yang, Lixing, Kucherlapati, Melanie, Chen, Fengju, Hadjipanayis, Angela, Pantazi, Angeliki, Bristow, Christopher A., Lee, Eunjung A., Mahadeshwar, Harshad S., Tang, Jiabin, Zhang, Jianhua, Seth, Sahil, Lee, Semin, Ren, Xiaojia, Song, Xingzhi, Sun, Huandong, Seidman, Jonathan, Luquette, Lovelace J., Xi, Ruibin, Chin, Lynda, Protopopov, Alexei, Li, Wei, Park, Peter J., Kucherlapati, Raju, Creighton, Chad J.

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An enhanced genetic model of colorectal cancer progression history von Yang, Lixing, Wang, Su, Lee, Jake June-Koo, Lee, Semin, Lee, Eunjung, Shinbrot, Eve, Wheeler, David A, Kucherlapati, Raju, Park, Peter J

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Engineering and Functional Characterization of Fusion Genes Identifies Novel Oncogenic Drivers of Cancer von Lu, Hengyu, Villafane, Nicole, Dogruluk, Turgut, Grzeskowiak, Caitlin L, Kong, Kathleen, Tsang, Yiu Huen, Zagorodna, Oksana, Pantazi, Angeliki, Yang, Lixing, Neill, Nicholas J, Kim, Young Won, Creighton, Chad J, Verhaak, Roel G, Mills, Gordon B, Park, Peter J, Kucherlapati, Raju, Scott, Kenneth L

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Next-generation sequencing identifies rare variants associated with Noonan syndrome von Chen, Peng-Chieh, Yin, Jiani, Yu, Hui-Wen, Yuan, Tao, Fernande, Minerva, Yung, Christina K., Trinh, Quang M., Peltekova, Vanya D., Reid, Jeffrey G., Tworog-Dube, Erica, Morgan, Margaret B., Muzny, Donna M., Stein, Lincoln, McPherson, John D., Roberts, Amy E., Gibbs, Richard A., Neel, Benjamin G., Kucherlapati, Raju

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Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome von Tartaglia, Marco, Mehler, Ernest L, Goldberg, Rosalie, Zampino, Giuseppe, Brunner, Han G, Kremer, Hannie, van der Burgt, Ineke, Crosby, Andrew H, Ion, Andra, Jeffery, Steve, Kalidas, Kamini, Patton, Michael A, Kucherlapati, Raju S, Gelb, Bruce D

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Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model von Hiramoto, Takeshi, Kang, Gina, Suzuki, Go, Satoh, Yasushi, Kucherlapati, Raju, Watanabe, Yasuhiro, Hiroi, Noboru

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In vivo wide-area cellular imaging by side-view endomicroscopy von Yun, Seok H, Kim, Pilhan, Chung, Euiheon, Yamashita, Hiroshi, Hung, Kenneth E, Mizoguchi, Atsushi, Kucherlapati, Raju, Fukumura, Dai, Jain, Rakesh K

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Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion von Xi, Ruibin, Hadjipanayis, Angela G, Luquette, Lovelace J, Kim, Tae-Min, Lee, Eunjung, Zhang, Jianhua, Johnson, Mark D, Muzny, Donna M, Wheeler, David A, Gibbs, Richard A, Kucherlapati, Raju, Park, Peter J

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Medical complications, clinical findings, and educational outcomes in adults with Noonan syndrome von Smpokou, Patroula, Tworog-Dube, Erica, Kucherlapati, Raju S., Roberts, Amy E.

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