Low-copy piggyBac transposon mutagenesis in mice identifies genes driving melanoma

nork Ni, Thomas K., Landrette, Sean F., Bjornson, Robert D., Bosenberg, Marcus W., Xu, Tian
Argitaratua 2013

Integrating Sequencing Technologies in Personal Genomics: Optimal Low Cost Reconstruction of Structural Variants

nork Du, Jiang, Bjornson, Robert D., Zhang, Zhengdong D., Kong, Yong, Snyder, Michael, Gerstein, Mark B.
Argitaratua 2009

A spatial simulation approach to account for protein structure when identifying non-random somatic mutations

nork Ryslik, Gregory A, Cheng, Yuwei, Cheung, Kei-Hoi, Bjornson, Robert D, Zelterman, Daniel, Modis, Yorgo, Zhao, Hongyu
Argitaratua izan da BMC Bioinformatics (2014)

Analysis of membrane proteins in metagenomics: Networks of correlated environmental features and protein families

nork Patel, Prianka V., Gianoulis, Tara A., Bjornson, Robert D., Yip, Kevin Y., Engelman, Donald M., Gerstein, Mark B.
Argitaratua 2010

Influence of Host Phylogeographic Patterns and Incomplete Lineage Sorting on Within-Species Genetic Variability in Wigglesworthia Species, Obligate Symbionts of Tsetse Flies

nork Symula, Rebecca E., Marpuri, Ian, Bjornson, Robert D., Okedi, Loyce, Beadell, Jon, Alam, Uzma, Aksoy, Serap, Caccone, Adalgisa
Argitaratua 2011

X!!Tandem, an Improved Method for Running X!Tandem in Parallel on Collections of Commodity Computers

nork Bjornson, Robert D., Carriero, Nicholas J., Colangelo, Christopher, Shifman, Mark, Cheung, Kei-Hoi, Miller, Perry L., Williams, Kenneth
Argitaratua 2007

Insight into the Transmission Biology and Species-Specific Functional Capabilities of Tsetse (Diptera: Glossinidae) Obligate Symbiont Wigglesworthia

nork Rio, Rita V. M., Symula, Rebecca E., Wang, Jingwen, Lohs, Claudia, Wu, Yi-neng, Snyder, Anna K., Bjornson, Robert D., Oshima, Kenshiro, Biehl, Bryan S., Perna, Nicole T., Hattori, Masahira, Aksoy, Serap
Argitaratua 2012

Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population

nork Lee, Sangmoon, Seo, Jihae, Park, Jinman, Nam, Jae-Yong, Choi, Ahyoung, Ignatius, Jason S., Bjornson, Robert D., Chae, Jong-Hee, Jang, In-Jin, Lee, Sanghyuk, Park, Woong-Yang, Baek, Daehyun, Choi, Murim
Argitaratua izan da Sci Rep (2017)

YPED: An Integrated Bioinformatics Suite and Database for Mass Spectrometry-based Proteomics Research

nork Colangelo, Christopher M., Shifman, Mark, Cheung, Kei-Hoi, Stone, Kathryn L., Carriero, Nicholas J., Gulcicek, Erol E., Lam, TuKiet T., Wu, Terence, Bjornson, Robert D., Bruce, Can, Nairn, Angus C., Rinehart, Jesse, Miller, Perry L., Williams, Kenneth R.
Argitaratua izan da Genomics Proteomics Bioinformatics (2015)

Genomic landscape of cutaneous T cell lymphoma

nork Choi, Jaehyuk, Goh, Gerald, Walradt, Trent, Hong, Bok S., Bunick, Christopher G., Chen, Kan, Bjornson, Robert D., Maman, Yaakov, Wang, Tiffany, Tordoff, Jesse, Carlson, Kacie, Overton, John D., Liu, Kristina J., Lewis, Julia M., Devine, Lesley, Barbarotta, Lisa, Foss, Francine M., Subtil, Antonio, Vonderheid, Eric C., Edelson, Richard L., Schatz, David G., Boggon, Titus J., Girardi, Michael, Lifton, Richard P.
Argitaratua izan da Nat Genet (2015)

De novo mutations revealed by whole exome sequencing are strongly associated with autism

nork Sanders, Stephan J., Murtha, Michael T., Gupta, Abha R., Murdoch, John D., Raubeson, Melanie J., Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, DiLullo, Nicholas M., Parikshak, Neelroop N., Stein, Jason L., Walker, Michael F., Ober, Gordon T., Teran, Nicole A., Song, Youeun, El-Fishawy, Paul, Murtha, Ryan C., Choi, Murim, Overton, John D., Bjornson, Robert D., Carriero, Nicholas J., Meyer, Kyle A., Bilguvar, Kaya, Mane, Shrikant M., Šestan, Nenad, Lifton, Richard P., Günel, Murat, Roeder, Kathryn, Geschwind, Daniel H., Devlin, Bernie, State, Matthew W.
Argitaratua 2012

Keck Foundation Biotechnology Resource Laboratory, Yale University

nork Stone, Kathryn L., Bjornson, Robert D., Blasko, Gregory G., Bruce, Can, Cofrancesco, Renee, Carriero, Nicholas J., Colangelo, Christopher M., Crawford, Janet K., Crawford, J. Myron, daSilva, Nancy C., Deluca, Joseph D., Elliott, James I., Elliott, Margaret M., Flory, P. John, Folta-Stogniew, Ewa J., Gulcicek, Erol, Kong, Yong, Lam, TuKiet T., Lee, Ji Y., Lin, Aiping, LoPresti, Mary B., Mane, Shrikant M., McMurray, Walter J., Tikhonova, Irina R., Westman, Sheila, Williams, Nancy A., Wu, Terence L., Hongyu, Zhao, Williams, Kenneth R.
Argitaratua 2008

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

nork 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, Gaynor, 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
Argitaratua izan da Nat Genet (2017)

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus

nork Furey, Charuta Gavankar, Choi, Jungmin, Jin, Sheng Chih, Zeng, Xue, Timberlake, Andrew T., Nelson-Williams, Carol, Mansuri, M. Shahid, Lu, Qiongshi, Duran, Daniel, Panchagnula, Shreyas, Allocco, August, Karimy, Jason K., Khanna, Arjun, Gaillard, Jonathan R., DeSpenza, Tyrone, Antwi, Prince, Loring, Erin, Butler, William E., Smith, Edward R., Warf, Benjamin C., Strahle, Jennifer M., Limbrick, David D., Storm, Phillip B., Heuer, Gregory, Jackson, Eric M., Iskandar, Bermans J., Johnston, James M., Tikhonova, Irina, Castaldi, Christopher, López-Giráldez, Francesc, Bjornson, Robert D., Knight, James R., Bilguvar, Kaya, Mane, Shrikant, Alper, Seth L., Haider, Shozeb, Guclu, Bulent, Bayri, Yasar, Sahin, Yener, Apuzzo, Michael L.J., Duncan, Charles C., DiLuna, Michael L., Günel, Murat, Lifton, Richard P., Kahle, Kristopher T.
Argitaratua izan da Neuron (2018)

De novo mutations in histone modifying genes in congenital heart disease

nork Zaidi, Samir, Choi, Murim, Wakimoto, Hiroko, Ma, Lijiang, Jiang, Jianming, Overton, John D., Romano-Adesman, Angela, Bjornson, Robert D., Breitbart, Roger E., Brown, Kerry K., Carriero, Nicholas J., Cheung, Yee Him, Deanfield, John, DePalma, Steve, Fakhro, Khalid A., Glessner, Joseph, Hakonarson, Hakon, Italia, Michael, Kaltman, Jonathan R., Kaski, Juan, Kim, Richard, Kline, Jennie K., Lee, Teresa, Leipzig, Jeremy, Lopez, Alexander, Mane, Shrikant M., Mitchell, Laura E., Newburger, Jane W., Parfenov, Michael, Pe'er, Itsik, Porter, George, Roberts, Amy, Sachidanandam, Ravi, Sanders, Stephan J., Seiden, Howard S., State, Mathew W., Subramanian, Sailakshmi, Tikhonova, Irina R., Wang, Wei, Warburton, Dorothy, White, Peter S., Williams, Ismee A., Zhao, Hongyu, Seidman, Jonathan G., Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Seidman, Christine E., Lifton, Richard P.
Argitaratua 2013