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Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements., Wang, Feng, Wang Hui, Tuan Han-Fang, Nguyen Duy H., Sun Vincent, Keser Vafa, Bowne Sara J., Sullivan Lori S., Luo Hongrong, Zhao Ling, et al. , Human genetics, 2013 Oct 24, (2013) Abstract
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements., Wang, Feng, Wang Hui, Tuan Han-Fang, Nguyen Duy H., Sun Vincent, Keser Vafa, Bowne Sara J., Sullivan Lori S., Luo Hongrong, Zhao Ling, et al. , Human genetics, 2014 Mar, Volume 133, Issue 3, p.331-45, (2014) Abstract
Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients., Salvo, Jason, Lyubasyuk Vera, Xu Mingchu, Wang Hui, Wang Feng, Nguyen Duy, Wang Keqing, Luo Hongrong, Wen Cindy, Shi Catherine, et al. , Investigative ophthalmology & visual science, 2015, Volume 56, Issue 3, p.1937-46, (2015) Abstract
Next-generation sequencing identifies rare variants associated with Noonan syndrome, Chen, P. - C., Yin J., Yu H. - W., Yuan T., Fernandez M., Yung C. K., Trinh Q. M., Peltekova V. D., Reid J. G., Tworog-Dube E., et al. , Proceedings of the National Academy of Sciences, 08/2014, Volume 111, Issue 31, p.11473 - 11478, (2014)
Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa., Fu, Qing, Wang Feng, Wang Hui, Xu Fei, Zaneveld Jacques E., Ren Huanan, Keser Vafa, Lopez Irma, Tuan Han-Fang, Salvo Jason S., et al. , Investigative ophthalmology & visual science, 2013 Jun, Volume 54, Issue 6, p.4158-66, (2013) Abstract
No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects., Baumert, Jens, Huang Jie, McKnight Barbara, Sabater-Lleal Maria, Steri Maristella, Chu Audrey Y., Trompet Stella, Lopez Lorna M., Fornage Myriam, Teumer Alexander, et al. , PloS one, 2014, Volume 9, Issue 12, p.e111156, (2014) Abstract
Nonhuman primates as models for studies of prostate specific antigen and prostatic diseases., Mubiru, James N., Hubbard Gene B., Dick Edward J., Furman Jaime, Troyer Dean A., and Rogers Jeffrey , The Prostate, 2008 Oct 1, Volume 68, Issue 14, p.1546-54, (2008) Abstract
Notch Activation as a Driver of Osteogenic Sarcoma., Tao, Jianning, Jiang Ming-Ming, Jiang Lichun, Salvo Jason S., Zeng Huan-Chang, Dawson Brian, Bertin Terry K., Rao Pulivarthi H., Chen Rui, Donehower Lawrence A., et al. , Cancer cell, 2014 Sep 8, Volume 26, Issue 3, p.390-401, (2014) Abstract
A novel beta-thalassaemia mutation in the 5' untranslated region of the beta-globin gene., Athanassiadou, A., Papachatzopoulou A., Zoumbos N., Maniatis G. M., and Gibbs R. , British journal of haematology, 1994 Oct, Volume 88, Issue 2, p.307-10, (1994) Abstract
Novel genetic causes for cerebral visual impairment., Bosch, Daniëlle G. M., Boonstra Nienke F., de Leeuw Nicole, Pfundt Rolph, Nillesen Willy M., de Ligt Joep, Gilissen Christian, Jhangiani Shalini, Lupski James R., Cremers Frans P. M., et al. , European journal of human genetics : EJHG, 2015 Sep 9, (2015) Abstract
Novel microRNA candidates and miRNA-mRNA pairs in embryonic stem (ES) cells., Gu, Peili, Reid Jeffrey G., Gao Xiaolian, Shaw Chad A., Creighton Chad, Tran Peter L., Zhou Xiaochuan, Drabek Rafal B., Steffen David L., Hoang David M., et al. , PloS one, 2008, Volume 3, Issue 7, p.e2548, (2008) Abstract
Novel potential ALL low-risk markers revealed by gene expression profiling with new high-throughput SSH-CCS-PCR., Qiu, J., Gunaratne P., Peterson L. E., Khurana D., Walsham N., Loulseged H., Karni R. J., Roussel E., Gibbs R. A., Margolin J. F., et al. , Leukemia, 2003 Sep, Volume 17, Issue 9, p.1891-900, (2003) Abstract
Novel somatic and germline mutations in intracranial germ cell tumours., Wang, Linghua, Yamaguchi Shigeru, Burstein Matthew D., Terashima Keita, Chang Kyle, Ng Ho-Keung, Nakamura Hideo, He Zongxiao, Doddapaneni Harshavardhan, Lewis Lora, et al. , Nature, 2014 Jun 4, (2014) Abstract
NR2F1 mutations cause optic atrophy with intellectual disability., Bosch, Daniëlle G. M., Boonstra Nienke F., Gonzaga-Jauregui Claudia, Xu Mafei, de Ligt Joep, Jhangiani Shalini, Wiszniewski Wojciech, Muzny Donna M., Yntema Helger G., Pfundt Rolph, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.303-9, (2014) Abstract
Nuclear DNA polymorphisms in a wild population of yellow baboons (Papio hamadryas cynocephalus) from Mikumi National Park, Tanzania., Rogers, J., and Kidd K. K. , American journal of physical anthropology, 1993 Apr, Volume 90, Issue 4, p.477-86, (1993) Abstract
nWayComp: a genome-wide sequence comparison tool for multiple strains/species of phylogenetically related microorganisms., Yao, Jiqiang, Lin Hong, Doddapaneni Harshavardhan, and Civerolo Edwin L. , In silico biology, 2007, Volume 7, Issue 2, p.195-200, (2007) Abstract
Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients., Scollon, Sarah, Bergstrom Katie, Kerstein Robin A., Wang Tao, Hilsenbeck Susan G., Ramamurthy Uma, Gibbs Richard A., Eng Christine M., Chintagumpala Murali M., Berg Stacey L., et al. , Genome medicine, 2014, Volume 6, Issue 9, p.69, (2014) Abstract
OikoBase: a genomics and developmental transcriptomics resource for the urochordate Oikopleura dioica., Danks, Gemma, Campsteijn Coen, Parida Mrutyunjaya, Butcher Stephen, Doddapaneni Harsha, Fu Bolei, Petrin Raul, Metpally Raghu, Lenhard Boris, Wincker Patrick, et al. , Nucleic acids research, 2013 Jan, Volume 41, Issue Database issue, p.D845-53, (2013) Abstract
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders., Schaaf, Christian P., Sabo Aniko, Sakai Yasunari, Crosby Jacy, Muzny Donna, Hawes Alicia, Lewis Lora, Akbar Humeira, Varghese Robin, Boerwinkle Eric, et al. , Human molecular genetics, 2011 Sep 1, Volume 20, Issue 17, p.3366-75, (2011) Abstract
On the genetic architecture of cortical folding and brain volume in primates., Rogers, Jeffrey, Kochunov Peter, Zilles Karl, Shelledy Wendy, Lancaster Jack, Thompson Paul, Duggirala Ravindranath, Blangero John, Fox Peter T., and Glahn David C. , NeuroImage, 2010 Nov 15, Volume 53, Issue 3, p.1103-8, (2010) Abstract
Oncodevelopmental and hormonal regulation of alpha 1-fetoprotein gene expression., Belanger, L., Baril P., Guertin M., Gingras M. C., Gourdeau H., Anderson A., Hamel D., and Boucher J. M. , Advances in enzyme regulation, 1983, Volume 21, p.73-99, (1983) Abstract
Onset of atonal expression in Drosophila retinal progenitors involves redundant and synergistic contributions of Ey/Pax6 and So binding sites within two distant enhancers., Zhou, Qingxiang, Zhang Tianyi, Jemc Jennifer C., Chen Yiyun, Chen Rui, Rebay Ilaria, and Pignoni Francesca , Developmental biology, 2014 Feb 1, Volume 386, Issue 1, p.152-64, (2014) Abstract
Open access data sharing in genomic research., Pereira, Stacey, Gibbs Richard A., and McGuire Amy L. , Genes, 2014, Volume 5, Issue 3, p.739-47, (2014) Abstract
Orphan nuclear receptor GCNF is required for the repression of pluripotency genes during retinoic acid-induced embryonic stem cell differentiation., Gu, Peili, LeMenuet Damien, Chung Arthur C. - K., Mancini Michael, Wheeler David A., and Cooney Austin J. , Molecular and cellular biology, 2005 Oct, Volume 25, Issue 19, p.8507-19, (2005) Abstract
Orphan nuclear receptor LRH-1 is required to maintain Oct4 expression at the epiblast stage of embryonic development., Gu, Peili, Goodwin Bryan, Chung Arthur C. - K., Xu Xueping, Wheeler David A., Price Roger R., Galardi Cristin, Peng Li, Latour Anne M., Koller Beverly H., et al. , Molecular and cellular biology, 2005 May, Volume 25, Issue 9, p.3492-505, (2005) Abstract

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