المؤلفون: Mahdieh, Nejat^{Aff1, Aff2}, Heidari, Morteza, Rezaei, Zahra, Tavasoli, Ali Reza^{Aff1, Aff3}, Hosseinpour, Sareh, Rasulinejad, Maryam, Dehnavi, Ali Zare, Ghahvechi Akbari, Masoud, Badv, Reza Shervin, Vafaei, Elahe, Mohebbi, Ali, Mohammadi, Pouria, Hosseiny, Seyyed Mohammad Mahdi, Azizimalamiri, Reza, Nikkhah, Ali^{Aff4, Aff7}, Pourbakhtyaran, Elham, Rohani, Mohammad, Khanbanha, Narges, Nikbakht, Sedigheh, Movahedinia, Mojtaba, Karimi, Parviz, Ghabeli, Homa, Hosseini, Seyed Ahmad, Rashidi, Fatemeh Sadat, Garshasbi, Masoud, Kashani, Morteza Rezvani, Ghiasvand, Noor M., Zuchner, Stephan, Synofzik, Matthis^{Aff18, Aff19}, Ashrafi, Mahmoud Reza^{Aff1, Aff20, IDs40246024005985_cor30}

المصدر: Human Genomics. 18(1)

المؤلفون: Miesfeld, Joel B, Ghiasvand, Noor M, Marsh-Armstrong, Brennan, Marsh-Armstrong, Nicholas, Miller, Eric B, Zhang, Pengfei, Manna, Suman K, Zawadzki, Robert J, Brown, Nadean L, Glaser, Tom

المصدر: Proceedings of the National Academy of Sciences of the United States of America. 117(35)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Ophthalmology and Optometry, Neurosciences, Genetics, Eye Disease and Disorders of Vision, Eye, Animals, Basic Helix-Loop-Helix Transcription Factors, Cell Differentiation, Embryo, Mammalian, Female, Gene Expression Regulation, Developmental, Male, Mice, Mice, Inbred C57BL, Nerve Tissue Proteins, Neurogenesis, Optic Nerve, Regulatory Sequences, Nucleic Acid, Retina, Retinal Ganglion Cells, Transcription Factors, glaucoma, shadow enhancer, optic disc area, optic nerve, human genetic disorders

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/54z557pk

المؤلفون: Ghiasvand, Noor M, Rudolph, Dellaney D, Mashayekhi, Mohammad, Brzezinski, Joseph A, Goldman, Daniel, Glaser, Tom

المصدر: Nature Neuroscience. 14(5)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Ophthalmology and Optometry, Neurosciences, Eye Disease and Disorders of Vision, Genetics, Eye, Adolescent, Animals, Animals, Genetically Modified, Basic Helix-Loop-Helix Transcription Factors, Child, Preschool, Chromosome Mapping, Chromosomes, Human, Pair 10, Computational Biology, Consanguinity, DNA Mutational Analysis, Embryo, Mammalian, Enhancer Elements, Genetic, Family Health, Female, Flow Cytometry, Gene Expression Regulation, Developmental, Humans, Iran, Luminescent Proteins, Magnetic Resonance Imaging, Male, Mice, Middle Aged, Neurogenesis, Polymorphism, Single Nucleotide, Retina, Retinal Detachment, Sequence Deletion, Superior Colliculi, Zebrafish, Psychology, Cognitive Sciences, Neurology & Neurosurgery, Biological psychology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0wg5b94d

المؤلفون: Ghiasvand, Noor M., Gholamhoseini, Hamideh, Rashidi, Fatemeh Sadat, Samarbafzadeh, Ehsan, Solgi, Ali, Ghiasvand, Reza, Yaghoubi, Fatemeh, Zabihi, Mohsen, BaniArdalan, Soha, Motejali, Masoomeh, Jahani, Zohreh, M. Sinclair, K. Szostak, Maghsoudi, Nader, Alireza Zali

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e02c66e1e129b83eae6158bbfcc47d24

المؤلفون: Friedman, James S., Ray, Joseph W., Waseem, Naushin, Johnson, Kory, Brooks, Matthew J., Hugosson, Therése, Breuer, Debra, Branham, Kari E., Krauth, Daniel S., Bowne, Sara J., Sullivan, Lori S., Ponjavic, Vesna, Gränse, Lotta, Khanna, Ritu, Trager, Edward H., Gieser, Linn M., Hughbanks-Wheaton, Dianna, Cojocaru, Radu I., Ghiasvand, Noor M., Chakarova, Christina F., Abrahamson, Magnus, Goering, Harald H. H., Webster, Andrew R., Birch, David G., Abecasis, Goncalo R., Fann, Yang, Bhattacharya, Shomi S., Daiger, Stephen P., Heckenlively, John R., Andréasson, Sten, Swaroop, Anand

المصدر: American Journal of Human Genetics. 84(6):792-800

مصطلحات موضوعية: Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

URL الوصول: https://lup.lub.lu.se/record/1441781
http://dx.doi.org/10.1016/j.ajhg.2009.05.007

المؤلفون: Ghiasvand, Noor M., Shirzad, Ebrahim, Naghavi, Mohsen, Mahdavi, Mohammad R. Vaez

المصدر: American Journal of Medical Genetics. Part A; 7 July 1998, Vol. 78 Issue: 3 p226-232, 7p

المؤلفون: Abecasis GR; Department of Biostatistics, University of Michigan, Ann Arbor, MI 48105, USA., Yashar BM, Zhao Y, Ghiasvand NM, Zareparsi S, Branham KE, Reddick AC, Trager EH, Yoshida S, Bahling J, Filippova E, Elner S, Johnson MW, Vine AK, Sieving PA, Jacobson SG, Richards JE, Swaroop A

المصدر: American journal of human genetics [Am J Hum Genet] 2004 Mar; Vol. 74 (3), pp. 482-94. Date of Electronic Publication: 2004 Feb 16.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Mapping* , Genetic Predisposition to Disease*, Macular Degeneration/*genetics, Aging/genetics ; Humans ; Statistics, Nonparametric