Evaluation of variant detection software for pooled next-generation sequence data

por Huang, Howard W., Mullikin, James C., Hansen, Nancy F.
Publicado 2015

The Sleep Inbred Panel, a Collection of Inbred Drosophila melanogaster with Extreme Long and Short Sleep Duration

por Serrano Negron, Yazmin L., Hansen, Nancy F., Harbison, Susan T.
Publicado 2018

Selection for long and short sleep duration in Drosophila melanogaster reveals the complex genetic network underlying natural variation in sleep

por Harbison, Susan T., Serrano Negron, Yazmin L., Hansen, Nancy F., Lobell, Amanda S.
Publicado 2017

Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans

por Liu, Zhi, Shriner, Daniel, Hansen, Nancy F., Rotimi, Charles N., Mullikin, James C.
Publicado 2020

NovoGraph: Human genome graph construction from multiple long-read de novo assemblies

por Biederstedt, Evan, Oliver, Jeffrey C., Hansen, Nancy F., Jajoo, Aarti, Dunn, Nathan, Olson, Andrew, Busby, Ben, Dilthey, Alexander T.
Publicado 2018

KLF3 and PAX6 are candidate driver genes in late-stage, MSI-hypermutated endometrioid endometrial carcinomas

por Rudd, Meghan L., Hansen, Nancy F., Zhang, Xiaolu, Urick, Mary Ellen, Zhang, Suiyuan, Merino, Maria J., Mullikin, James C., Brody, Lawrence C., Bell, Daphne W.
Publicado 2022

Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomas

por Pemov, Alexander, Dewan, Ramita, Hansen, Nancy F., Chandrasekharappa, Settara C., Ray-Chaudhury, Abhik, Jones, Kristine, Luo, Wen, Heiss, John D., Mullikin, James C., Chittiboina, Prashant, Stewart, Douglas R., Asthagiri, Ashok R.
Publicado 2020

First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial men...

por Dewan, Ramita, Pemov, Alexander, Dutra, Amalia S., Pak, Evgenia D., Edwards, Nancy A., Ray-Chaudhury, Abhik, Hansen, Nancy F., Chandrasekharappa, Settara C., Mullikin, James C., Asthagiri, Ashok R., Heiss, John D., Stewart, Douglas R., Germanwala, Anand V.
Publicado 2017

Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans

por Bentley, Amy R., Chen, Guanjie, Shriner, Daniel, Doumatey, Ayo P., Zhou, Jie, Huang, Hanxia, Mullikin, James C., Blakesley, Robert W., Hansen, Nancy F., Bouffard, Gerard G., Cherukuri, Praveen F., Maskeri, Baishali, Young, Alice C., Adeyemo, Adebowale, Rotimi, Charles N.
Publicado 2014

Somatic mutational landscape of AML with inv(16) or t(8;21) identifies patterns of clonal evolution in relapse leukemia

por Sood, Raman, Hansen, Nancy F., Donovan, Frank X., Carrington, Blake, Bucci, Donna, Maskeri, Baishali, Young, Alice, Trivedi, Niraj S., Kohlschmidt, Jessica, Stone, Richard M., Caligiuri, Michael A., Chandrasekharappa, Settara C., Marcucci, Guido, Mullikin, James C., Bloomfield, Clara D., Liu, Paul
Publicado 2015

Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates

por Blakesley, Robert W, Hansen, Nancy F, Gupta, Jyoti, McDowell, Jennifer C, Maskeri, Baishali, Barnabas, Beatrice B, Brooks, Shelise Y, Coleman, Holly, Haghighi, Payam, Ho, Shi-Ling, Schandler, Karen, Stantripop, Sirintorn, Vogt, Jennifer L, Thomas, Pamela J, Bouffard, Gerard G, Green, Eric D
Publicado 2010

Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1

por Rudd, Meghan L, Mohamed, Hassan, Price, Jessica C, O’Hara, Andrea J, Le Gallo, Matthieu, Urick, Mary Ellen, Cruz, Pedro, Zhang, Suiyuan, Hansen, Nancy F, Godwin, Andrew K, Sgroi, Dennis C, Wolfsberg, Tyra G, Mullikin, James C, Merino, Maria J, Bell, Daphne W
Publicado 2014

Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes

por Le Gallo, Matthieu, O’Hara, Andrea J., Rudd, Meghan L., Urick, Mary Ellen, Hansen, Nancy F., O’Neil, Nigel J., Price, Jessica C., Zhang, Suiyuan, England, Bryant M., Godwin, Andrew K., Sgroi, Dennis C., Hieter, Philip, Mullikin, James C., Merino, Maria J., Bell, Daphne W.
Publicado 2012

Light whole genome sequence for SNP discovery across domestic cat breeds

por Mullikin, James C, Hansen, Nancy F, Shen, Lei, Ebling, Heather, Donahue, William F, Tao, Wei, Saranga, David J, Brand, Adrianne, Rubenfield, Marc J, Young, Alice C, Cruz, Pedro, Driscoll, Carlos, David, Victor, Al-Murrani, Samer WK, Locniskar, Mary F, Abrahamsen, Mitchell S, O'Brien, Stephen J, Smith, Douglas R, Brockman, Jeffrey A
Publicado 2010

Mutational Signatures of De-Differentiation in Functional Non-Coding Regions of Melanoma Genomes

por Parker, Stephen C. J., Gartner, Jared, Cardenas-Navia, Isabel, Wei, Xiaomu, Ozel Abaan, Hatice, Ajay, Subramanian S., Hansen, Nancy F., Song, Lingyun, Bhanot, Umesh K., Killian, J. Keith, Gindin, Yevgeniy, Walker, Robert L., Meltzer, Paul S., Mullikin, James C., Furey, Terrence S., Crawford, Gregory E., Rosenberg, Steven A., Samuels, Yardena, Margulies, Elliott H.
Publicado 2012

Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases

por Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F., Teer, Jamie K., Hansen, Nancy F., Cruz, Pedro, Mullikin, James C., Blakesley, Robert W., Golas, Gretchen, Kwan, Justin, Sandler, Anthony, Fuentes Fajardo, Karin, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I., Langer, Thomas, Gahl, William A., Toro, Camilo
Publicado 2013

Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases

por Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F., Teer, Jamie K., Hansen, Nancy F., Cruz, Pedro, Mullikin for the NISC Comparative Sequencing Program, James C., Blakesley, Robert W., Golas, Gretchen, Kwan, Justin, Sandler, Anthony, Fuentes Fajardo, Karin, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I., Langer, Thomas, Gahl, William A., Toro, Camilo
Publicado 2011

Sequencing of Candidate Chromosome Instability Genes in Endometrial Cancers Reveals Somatic Mutations in ESCO1, CHTF18, and MRE11A

por Price, Jessica C., Pollock, Lana M., Rudd, Meghan L., Fogoros, Sarah K., Mohamed, Hassan, Hanigan, Christin L., Le Gallo, Matthieu, Program, NIH Intramural Sequencing Center (NISC) Comparative Sequencing, Zhang, Suiyuan, Cruz, Pedro, Cherukuri, Praveen F., Hansen, Nancy F., McManus, Kirk J., Godwin, Andrew K., Sgroi, Dennis C., Mullikin, James C., Merino, Maria J., Hieter, Philip, Bell, Daphne W.
Publicado 2013

Predisposition to Cancer Caused by Genetic and Functional Defects of Mammalian Atad5

por Bell, Daphne W., Sikdar, Nilabja, Lee, Kyoo-young, Price, Jessica C., Chatterjee, Raghunath, Park, Hee-Dong, Fox, Jennifer, Ishiai, Masamichi, Rudd, Meghan L., Pollock, Lana M., Fogoros, Sarah K., Mohamed, Hassan, Hanigan, Christin L., Zhang, Suiyuan, Cruz, Pedro, Renaud, Gabriel, Hansen, Nancy F., Cherukuri, Praveen F., Borate, Bhavesh, McManus, Kirk J., Stoepel, Jan, Sipahimalani, Payal, Godwin, Andrew K., Sgroi, Dennis C., Merino, Maria J., Elliot, Gene, Elkahloun, Abdel, Vinson, Charles, Takata, Minoru, Mullikin, James C., Wolfsberg, Tyra G., Hieter, Philip, Lim, Dae-Sik, Myung, Kyungjae
Publicado 2011

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

por Davis, Erica E., Zhang, Qi, Liu, Qin, Diplas, Bill H., Davey, Lisa M., Hartley, Jane, Stoetzel, Corinne, Szymanska, Katarzyna, Ramaswami, Gokul, Logan, Clare V., Muzny, Donna M., Young, Alice C., Wheeler, David A., Cruz, Pedro, Morgan, Margaret, Lewis, Lora R., Cherukuri, Praveen, Maskeri, Baishali, Hansen, Nancy F., Mullikin, James C., Blakesley, Robert W., Bouffard, Gerard G., Gyapay, Gabor, Reiger, Susanne, Tönshoff, Burkhard, Kern, Ilse, Soliman, Neveen A., Neuhaus, Thomas J., Swoboda, Kathryn J., Kayserili, Hulya, Gallagher, Tomas E., Lewis, Richard A., Bergmann, Carsten, Otto, Edgar A., Saunier, Sophie, Scambler, Peter J., Beales, Philip L., Gleeson, Joseph G., Maher, Eamonn R., Attié-Bitach, Tania, Dollfus, Hélène, Johnson, Colin A., Green, Eric D., Gibbs, Richard A., Hildebrandt, Friedhelm, Pierce, Eric A., Katsanis, Nicholas
Publicado 2011