SNPs in human miRNA genes affect biogenesis and function von Sun, Guihua, Yan, Jin, Noltner, Katie, Feng, Jinong, Li, Haitang, Sarkis, Daniel A, Sommer, Steve S, Rossi, John J

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Beyond Li Fraumeni Syndrome: Clinical Characteristics of Families With p53 Germline Mutations von GONZALEZ, Kelly D, NOLTNER, Katie A, WEITZEL, Jeffrey N, BUZIN, Carolyn H, DONGQING GU, WEN-FONG, Cindy Y, NGUYEN, Vu Q, HAN, Jennifer H, LOWSTUTER, Katrina, LONGMATE, Jeffrey, SOMMER, Steve S

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Evidence for X-chromosomal schizophrenia associated with microRNA alterations von Feng, Jinong, Sun, Guihua, Yan, Jin, Noltner, Katie, Li, Wenyan, Buzin, Carolyn H, Longmate, Jeff, Heston, Leonard L, Rossi, John, Sommer, Steve S

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High frequency of neurexin 1β signal peptide structural variants in patients with autism von Feng, Jinong, Schroer, Richard, Yan, Jin, Song, Wenjia, Yang, Chunmei, Bockholt, Anke, Cook, Edwin H., Skinner, Cindy, Schwartz, Charles E., Sommer, Steve S.

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Analysis of cancer mutation signatures in blood by a novel ultra-sensitive assay: monitoring of therapy or recurrence in non-metastatic breast cancer von Chen, Zhenbin, Feng, Jinong, Buzin, Carolyn H, Liu, Qiang, Weiss, Lawrence, Kernstine, Kemp, Somlo, George, Sommer, Steve S

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Neurexin 1α structural variants associated with autism von Yan, Jin, Noltner, Katie, Feng, Jinong, Li, Wenyan, Schroer, Richard, Skinner, Cindy, Zeng, Wenqi, Schwartz, Charles E., Sommer, Steve S.

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Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia von Song, Wenjia, Li, Wenyan, Feng, Jinong, Heston, Leonard L., Scaringe, William A., Sommer, Steve S.

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Epidemiology of doublet/multiplet mutations in lung cancers: evidence that a subset arises by chronocoordinate events von Chen, Zhenbin, Feng, Jinong, Buzin, Carolyn H, Sommer, Steve S

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Missense Mutations in the MEFV Gene Are Associated with Fibromyalgia Syndrome and Correlate with Elevated IL-1β Plasma Levels von Feng, Jinong, Zhang, Zhifang, Li, Wenyan, Shen, Xiaoming, Song, Wenjia, Yang, Chunmei, Chang, Frances, Longmate, Jeffrey, Marek, Claudia, St. Amand, R. Paul, Krontiris, Theodore G., Shively, John E., Sommer, Steve S.

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Evidence for mutation showers von Wang, Jicheng, Gonzalez, Kelly D, Scaringe, William A, Tsai, Kimberly, Liu, Ning, Gu, Dongqing, Li, Wenyan, Hill, Kathleen A, Sommer, Steve S

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Three ways of combining genotyping and resequencing in case-control association studies von Longmate, Jeffrey A, Larson, Garrett P, Krontiris, Theodore G, Sommer, Steve S

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Detection of ultrarare somatic mutation in the human TP53 gene by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification von Shi, Jinxiu, Liu, Qiang, Sommer, Steve S.

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Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers von Cohn, Jonathan A., Neoptolemos, John P., Feng, Jinong, Yan, Jin, Jiang, Zefei, Greenhalf, William, McFaul, Christopher, Mountford, Roger, Sommer, Steve S.

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Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder von Song, Wenjia, Li, Wenyan, Noltner, Katie, Yan, Jin, Green, Elaine, Grozeva, Detelina, Jones, Ian R., Craddock, Nick, Longmate, Jeff, Feng, Jinong, Sommer, Steve S.

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mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin von Yang, Chunmei, Feng, Jinong, Song, Wenjia, Wang, Jicheng, Tsai, Becky, Zhang, Yunwu, Scaringe, William A, Hill, Kathleen A, Margaritis, Paris, High, Katherine A, Sommer, Steve S

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MECP2 structural and 3′-UTR variants in schizophrenia, autism and other psychiatric diseases: A possible association with autism von Shibayama, Akane, Cook Jr, Edwin H., Feng, Jinong, Glanzmann, Cecile, Yan, Jin, Craddock, Nick, Jones, Ian R., Goldman, David, Heston, Leonard L., Sommer, Steve S.

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Analysis of the neuroligin 4Y gene in patients with autism von Yan, Jin, Feng, Jinong, Schroer, Richard, Li, Wenyan, Skinner, Cindy, Schwartz, Charles E, Cook, Jr, Edwin H, Sommer, Steve S

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Conversion Analysis for Mutation Detection in MLH1 and MSH2 in Patients With Colorectal Cancer von Casey, Graham, Lindor, Noralane M, Papadopoulos, Nickolas, Thibodeau, Stephen N, Moskow, John, Steelman, Scott, Buzin, Carolyn H, Sommer, Steve S, Collins, Christine E, Butz, Malinda, Aronson, Melyssa, Gallinger, Steven, Barker, Melissa A, Young, Joanne P, Jass, Jeremy R, Hopper, John L, Diep, Anh, Bapat, Bharati, Salem, Michael, Seminara, Daniela, Haile, Robert, Colon Cancer Family Registry, for the

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Microarray-based DNA resequencing using 3′ blocked primers von Sram, Jakub, Sommer, Steve S., Liu, Qiang

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Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotide von Buzin, Carolyn H., Feng, Jinong, Yan, Jin, Scaringe, William, Liu, Qiang, den Dunnen, Johan, Mendell, Jerry R., Sommer, Steve S.

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