Nadav Ahituv
Nadav Ahituv
Verifisert e-postadresse på ucsf.edu - Startside
Sitert av
Sitert av
In vivo enhancer analysis of human conserved non-coding sequences
LA Pennacchio, N Ahituv, AM Moses, S Prabhakar, MA Nobrega, ...
Nature 444 (7118), 499-502, 2006
Massively parallel functional dissection of mammalian enhancers in vivo
RP Patwardhan, JB Hiatt, DM Witten, MJ Kim, RP Smith, D May, C Lee, ...
Nature biotechnology 30 (3), 265-270, 2012
A distal enhancer and an ultraconserved exon are derived from a novel retroposon
G Bejerano, CB Lowe, N Ahituv, B King, A Siepel, SR Salama, EM Rubin, ...
Nature 441 (7089), 87-90, 2006
A genome-wide framework for mapping gene regulation via cellular genetic screens
M Gasperini, AJ Hill, JL McFaline-Figueroa, B Martin, S Kim, MD Zhang, ...
Cell 176 (1), 377-390. e19, 2019
Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice
LS Andersson, M Larhammar, F Memic, H Wootz, D Schwochow, ...
Nature 488 (7413), 642-646, 2012
Chromatin connectivity maps reveal dynamic promoter–enhancer long-range associations
Y Zhang, CH Wong, RY Birnbaum, G Li, R Favaro, CY Ngan, J Lim, E Tai, ...
Nature 504 (7479), 306-310, 2013
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans
O Vahava, R Morell, ED Lynch, S Weiss, ME Kagan, N Ahituv, JE Morrow, ...
Science 279 (5358), 1950-1954, 1998
Deletion of ultraconserved elements yields viable mice
N Ahituv, Y Zhu, A Visel, A Holt, V Afzal, LA Pennacchio, EM Rubin
PLoS biology 5 (9), e234, 2007
Variant interpretation: functional assays to the rescue
LM Starita, N Ahituv, MJ Dunham, JO Kitzman, FP Roth, G Seelig, ...
The American Journal of Human Genetics 101 (3), 315-325, 2017
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activity
F Inoue, M Kircher, B Martin, GM Cooper, DM Witten, MT McManus, ...
Genome research 27 (1), 38-52, 2017
MYO6, the human homologue of the gene responsible for deafness in Snell’s waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss
S Melchionda, N Ahituv, L Bisceglia, T Sobe, F Glaser, R Rabionet, ...
The American Journal of Human Genetics 69 (3), 635-640, 2001
CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiency
N Matharu, S Rattanasopha, S Tamura, L Maliskova, Y Wang, A Bernard, ...
Science 363 (6424), eaau0629, 2019
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
JY An, K Lin, L Zhu, DM Werling, S Dong, H Brand, HZ Wang, X Zhao, ...
Science 362 (6420), eaat6576, 2018
Massively parallel decoding of mammalian regulatory sequences supports a flexible organizational model
RP Smith, L Taher, RP Patwardhan, MJ Kim, F Inoue, J Shendure, ...
Nature genetics 45 (9), 1021-1028, 2013
Decoding enhancers using massively parallel reporter assays
F Inoue, N Ahituv
Genomics 106 (3), 159-164, 2015
Coding exons function as tissue-specific enhancers of nearby genes
RY Birnbaum, EJ Clowney, O Agamy, MJ Kim, J Zhao, T Yamanaka, ...
Genome research 22 (6), 1059-1068, 2012
Medical sequencing at the extremes of human body mass
N Ahituv, N Kavaslar, W Schackwitz, A Ustaszewska, J Martin, S Hébert, ...
The American Journal of Human Genetics 80 (4), 779-791, 2007
The Notch ligand Jagged1 is required for inner ear sensory development
AE Kiernan, N Ahituv, H Fuchs, R Balling, KB Avraham, KP Steel, ...
Proceedings of the National Academy of Sciences 98 (7), 3873-3878, 2001
Enhancer interaction networks as a means for singular olfactory receptor expression
E Markenscoff-Papadimitriou, WE Allen, BM Colquitt, T Goh, KK Murphy, ...
Cell 159 (3), 543-557, 2014
Saturation mutagenesis of twenty disease-associated regulatory elements at single base-pair resolution
M Kircher, C Xiong, B Martin, M Schubach, F Inoue, RJA Bell, JF Costello, ...
Nature communications 10 (1), 3583, 2019
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