Conservative homologous recombination preferentially repairs DNA double-strand breaks in the S phase of the cell cycle in human cells N Saleh-Gohari, T Helleday Nucleic acids research 32 (12), 3683-3688, 2004 | 449 | 2004 |
Spontaneous homologous recombination is induced by collapsed replication forks that are caused by endogenous DNA single-strand breaks N Saleh-Gohari, HE Bryant, N Schultz, KM Parker, TN Cassel, T Helleday Molecular and cellular biology, 2005 | 421 | 2005 |
Poly (ADP‐ribose) polymerase (PARP‐1) has a controlling role in homologous recombination N Schultz, E Lopez, N Saleh‐Gohari, T Helleday Nucleic acids research 31 (17), 4959-4964, 2003 | 403 | 2003 |
The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells AZ Al-Minawi, N Saleh-Gohari, T Helleday Nucleic acids research 36 (1), 1-9, 2008 | 183 | 2008 |
The ERCC1/XPF endonuclease is required for completion of homologous recombination at DNA replication forks stalled by inter-strand cross-links AZ Al-Minawi, YF Lee, D Håkansson, F Johansson, C Lundin, ... Nucleic acids research 37 (19), 6400-6413, 2009 | 121 | 2009 |
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients A Haghighi, TB Haack, M Atiq, H Mottaghi, H Haghighi-Kakhki, RA Bashir, ... Orphanet journal of rare diseases 9, 1-12, 2014 | 94 | 2014 |
A missense mutation in the MBTPS2 gene underlies the X-linked form of Olmsted syndrome. A Haghighi, CA Scott, DS Poon, R Yaghoobi, N Saleh-Gohari, V Plagnol, ... The Journal of investigative dermatology 133 (2), 571-573, 2012 | 60 | 2012 |
Distribution of β-globin gene mutations in thalassemia minor population of Kerman Province, Iran N Saleh-Gohari, MR Bazrafshani Iranian journal of public health 39 (2), 69, 2010 | 45 | 2010 |
RAD51C (RAD51L2) is involved in maintaining centrosome number in mitosis A Renglin Lindh, N Schultz, N Saleh-Gohari, T Helleday Cytogenetic and genome research 116 (1-2), 38-45, 2007 | 34 | 2007 |
Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia A Setoodeh, A Haghighi, N Saleh-Gohari, S Ellard, A Haghighi Gene 519 (2), 295-297, 2013 | 33 | 2013 |
Whole‐exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar … A Haghighi, P Nikuei, H Haghighi‐Kakhki, N Saleh‐Gohari, S Baghestani, ... British Journal of Dermatology 168 (6), 1353-1356, 2013 | 29 | 2013 |
Spectrum of α-globin gene mutations in the Kerman Province of Iran N Saleh-Gohari, A Khosravi-Mashizi Hemoglobin 34 (5), 451-460, 2010 | 26 | 2010 |
Strand invasion involving short tract gene conversion is specifically suppressed in BRCA2-deficient hamster cells N Saleh-Gohari, T Helleday Oncogene 23 (56), 9136-9141, 2004 | 25 | 2004 |
Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II A Haghighi, H Verdin, H Haghighi-Kakhki, N Piri, NS Gohari, E De Baere Molecular vision 18, 211, 2012 | 24 | 2012 |
Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers N Saleh-Gohari, MK Bami, R Nikbakht, H Karimi-Maleh Journal of clinical pathology 68 (7), 562-566, 2015 | 22 | 2015 |
Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing Knobloch syndrome A Haghighi, A Tiwari, N Piri, G Nürnberg, N Saleh-Gohari, A Haghighi, ... PloS one 9 (11), e112747, 2014 | 21 | 2014 |
Quantification of circulating miR-517c-3p and miR-210-3p levels in preeclampsia RMA Nejad, K Saeidi, S Gharbi, Z Salari, N Saleh-Gohari Pregnancy Hypertension 16, 75-78, 2019 | 19 | 2019 |
Co-inheritance of sickle cell trait and thalassemia mutations in South central Iran N Saleh-Gohari, M Mohammadi-Anaie Iranian Journal of Public Health 41 (10), 81, 2012 | 19 | 2012 |
Identification of homozygous WFS1 mutations (p. Asp211Asn, p. Gln486*) causing severe Wolfram syndrome and first report of male fertility A Haghighi, A Haghighi, A Setoodeh, N Saleh-Gohari, D Astuti, TG Barrett European Journal of Human Genetics 21 (3), 347-351, 2013 | 16 | 2013 |
BRCA1 gene mutations in breast cancer patients from Kerman Province, Iran N Saleh-Gohari, M Mohammadi-Anaie, B Kalantari-Khandani Iranian journal of cancer prevention 5 (4), 210, 2012 | 16 | 2012 |