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ABB-4209-2020

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Scopus Author ID: 7801573435

Keywords

Medical Genetics

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Iran

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Employment (1)

Kerman University of Medical Sciences: Kerman, Kerman, IR

Associate Professor of Medical Genetics (Department of Genetics, School of Medicine)
Employment
Source: Self-asserted source
Nasrollah saleh-gohari

Works (27)

Haplotype analysis in carriers of β-globin gene mutation facilitates genetic counseling in β-thalassemia: A cross-sectional study in Kerman Province, Iran

Iranian Journal of Public Health
2020 | Journal article
EID:

2-s2.0-85088388454

Part of ISBN:

22516093 22516085
Contributors: Saleh-Gohari, N.; Saeidi, K.; Ziaadini-Dashtkhaki, S.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Quantification of circulating miR-517c-3p and miR-210-3p levels in preeclampsia

Pregnancy Hypertension
2019 | Journal article
DOI: 10.1016/j.preghy.2019.03.004
EID:

2-s2.0-85062946046

Part of ISBN:

22107797 22107789
Contributors: Nejad, R.M.A.; Saeidi, K.; Gharbi, S.; Salari, Z.; Saleh-Gohari, N.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

A novel homozygous frameshift mutation in the FUCA1 gene causes both severe and mild fucosidosis

Journal of Clinical Pathology
2018 | Journal article
DOI: 10.1136/jclinpath-2018-205074
EID:

2-s2.0-85049196304

Part of ISBN:

14724146 00219746
Contributors: Saleh-Gohari, N.; Saeidi, K.; Zeighaminejad, R.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

A novel splice site mutation of the ATM gene associated with ataxia telangiectasia

Iranian Journal of Child Neurology
2018 | Journal article
DOI: 10.22037/ijcn.v12i4.15397
EID:

2-s2.0-85053261813

Part of ISBN:

20080700 17354668
Contributors: Saeidi, K.; Saleh Gohari, N.; Mansouri Nejad, S.E.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Frequency of factor V Leiden (G1691A) and prothrombin (G20210A) polymorphisms in population of Kerman Province, Iran

Journal of Kerman University of Medical Sciences
2017 | Journal article
EID:

2-s2.0-85042141033

Part of ISBN:

20082843 10239510
Contributors: Saleh-Gohari, N.; Salmani-Cheharfarsakhi, N.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

The association between preeclampsia and defined polymorphisms in prothrombin and coagulation factor V genes

Journal of Kerman University of Medical Sciences
2016 | Journal article
EID:

2-s2.0-84990068187

Part of ISBN:

20082843 10239510
Contributors: Salari, Z.; Saleh-Gohari, N.; Zainali, N.; Salmani-Cheharfarsakhi, N.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Effects of α-thalassaemia mutations on the haematological parameters of β-thalassaemia carriers

Journal of Clinical Pathology
2015 | Journal article
DOI: 10.1136/jclinpath-2014-202825
EID:

2-s2.0-84933182868

Part of ISBN:

14724146 00219746
Contributors: Saleh-Gohari, N.; Bami, M.K.; Nikbakht, R.; Karimi-Maleh, H.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Homozygosity mapping and whole exome sequencing reveal a novel homozygous COL18A1 mutation causing knobloch syndrome

PLoS ONE
2014 | Journal article
DOI: 10.1371/journal.pone.0112747
EID:

2-s2.0-84911490357

Part of ISBN:

19326203
Contributors: Haghighi, A.; Tiwari, A.; Piri, N.; Nürnberg, G.; Saleh-Gohari, N.; Haghighi, A.; Neidhardt, J.; Nürnberg, P.; Berger, W.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Sengers syndrome: Six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients

Orphanet Journal of Rare Diseases
2014 | Journal article
DOI: 10.1186/s13023-014-0119-3
EID:

2-s2.0-84908020091

Part of ISBN:

17501172
Contributors: Haghighi, A.; Haack, T.B.; Atiq, M.; Mottaghi, H.; Haghighi-Kakhki, H.; Bashir, R.A.; Ahting, U.; Feichtinger, R.G.; Mayr, J.A.; Rötig, A. et al.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

A missense mutation in the MBTPS2 gene underlies the x-linked form of olmsted syndrome

Journal of Investigative Dermatology
2013 | Journal article
DOI: 10.1038/jid.2012.289
EID:

2-s2.0-84872600970

Part of ISBN:

15231747 0022202X
Contributors: Haghighi, A.; Scott, C.A.; Poon, D.S.; Yaghoobi, R.; Saleh-Gohari, N.; Plagnol, V.; Kelsell, D.P.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Congenital insensitivity to pain with anhidrosis in an Iranian Patient

Basic and Clinical Neuroscience
2013 | Journal article
EID:

2-s2.0-84874966088

Part of ISBN:

2008126X
Contributors: Saleh-Gohari, N.; Mohammadi-Anaie, M.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia

Gene
2013 | Journal article
DOI: 10.1016/j.gene.2013.02.008
EID:

2-s2.0-84875590135

Part of ISBN:

03781119 18790038
Contributors: Setoodeh, A.; Haghighi, A.; Saleh-Gohari, N.; Ellard, S.; Haghighi, A.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility

European Journal of Human Genetics
2013 | Journal article
DOI: 10.1038/ejhg.2012.154
EID:

2-s2.0-84874114988

Part of ISBN:

10184813 14765438
Contributors: Haghighi, A.; Haghighi, A.; Setoodeh, A.; Saleh-Gohari, N.; Astuti, D.; Barrett, T.G.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Whole-exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosis

British Journal of Dermatology
2013 | Journal article
DOI: 10.1111/bjd.12151
EID:

2-s2.0-84878638695

Part of ISBN:

00070963 13652133
Contributors: Haghighi, A.; Nikuei, P.; Haghighi-Kakhki, H.; Saleh-Gohari, N.; Baghestani, S.; Krawitz, P.M.; Hecht, J.; Mundlos, S.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

BRCA1 gene mutations in breast cancer patients from Kerman province, Iran

Iranian Journal of Cancer Prevention
2012 | Journal article
EID:

2-s2.0-84867868544

Part of ISBN:

20082401
Contributors: Saleh-gohari, N.; Mohammadi-anaie, M.; Kalantari-khandani, B.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Co-inheritance of sickle cell trait and Thalassemia mutations in South Central Iran

Iranian Journal of Public Health
2012 | Journal article
EID:

2-s2.0-84867808095

Part of ISBN:

22516093 22516085
Contributors: Saleh-Gohari, N.; Mohammadi-Anaie, M.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Senior-Loken syndrome secondary to NPHP5/IQCB1 mutation in an Iranian family

NDT Plus
2011 | Journal article
DOI: 10.1093/ndtplus/sfr096
EID:

2-s2.0-84856333376

Part of ISBN:

17530784 17530792
Contributors: Haghighi, A.; Al-Hamed, M.; Al-Hissi, S.; Hynes, A.-M.; Sharifian, M.; Roozbeh, J.; Saleh-Gohari, N.; Sayer, J.A.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Distribution of β-globin gene mutations in thalassemia minor population of kerman province, Iran

Iranian Journal of Public Health
2010 | Journal article
EID:

2-s2.0-77954058615

Part of ISBN:

22516093 22516085
Contributors: Saleh-Gohari, N.; Bazrafshani, M.R.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Spectrum of α-globin gene mutations in the Kerman province of Iran

Hemoglobin
2010 | Journal article
DOI: 10.3109/03630269.2010.511587
EID:

2-s2.0-77956943192

Part of ISBN:

03630269 1532432X
Contributors: Saleh-Gohari, N.; Khosravi-Mashizi, A.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

A family with the 619 bp deletion on the β-globin gene found in Kerman Province, Iran

Hemoglobin
2009 | Journal article
DOI: 10.3109/03630260903335935
EID:

2-s2.0-72049125377

Part of ISBN:

03630269 1532432X
Contributors: Saleh-Gohari, N.; Mashizi, A.K.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

The ERCC1/XPF endonuclease is required for completion of homologous recombination at DNA replication forks stalled by inter-strand cross-links

Nucleic Acids Research
2009 | Journal article
DOI: 10.1093/nar/gkp705
EID:

2-s2.0-70450224524

Part of ISBN:

03051048 13624962
Contributors: Al-Minawi, A.Z.; Lee, Y.-F.; Håkansson, D.; Johansson, F.; Lundin, C.; Saleh-Gohari, N.; Schultz, N.; Jenssen, D.; Bryant, H.E.; Meuth, M. et al.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells

Nucleic Acids Research
2008 | Journal article
DOI: 10.1093/nar/gkm888
EID:

2-s2.0-38349098477

Part of ISBN:

03051048 13624962
Contributors: Al-minawi, A.Z.; Saleh-gohari, N.; Helleday, T.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

RAD51C (RAD51L2) is involved in maintaining centrosome number in mitosis

Cytogenetic and Genome Research
2007 | Journal article
DOI: 10.1159/000097416
EID:

2-s2.0-33846707466

Part of ISBN:

14248581
Contributors: Renglin Lindh, A.; Schultz, N.; Saleh-Gohari, N.; Helleday, T.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Spontaneous homologous recombination is induced by collapsed replication forks that are caused by endogenous DNA single-strand breaks

Molecular and Cellular Biology
2005 | Journal article
DOI: 10.1128/MCB.25.16.7158-7169.2005
EID:

2-s2.0-23344444636

Part of ISBN:

02707306
Contributors: Saleh-Gohari, N.; Bryant, H.E.; Schultz, N.; Parker, K.M.; Cassel, T.N.; Helleday, T.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Conservative homologous recombination preferentially repairs DNA double-strand breaks in the S phase of the cell cycle un human cells

Nucleic Acids Research
2004 | Journal article
DOI: 10.1093/nar/gkh703
EID:

2-s2.0-3142768860

Part of ISBN:

03051048
Contributors: Saleh-Gohari, N.; Helleday, T.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Strand invasion involving short tract gene conversion is specifically suppressed in BRCA2-deficient hamster cells

Oncogene
2004 | Journal article
DOI: 10.1038/sj.onc.1208178
EID:

2-s2.0-10944247548

Part of ISBN:

09509232
Contributors: Saleh-Gohari, N.; Helleday, T.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier

Poly(ADP-ribose) polymerase (PARP-1) has a controlling role in homologous recombination

Nucleic Acids Research
2003 | Journal article
DOI: 10.1093/nar/gkg703
EID:

2-s2.0-0344875495

Part of ISBN:

03051048
Contributors: Schultz, N.; Lopez, E.; Saleh-Gohari, N.; Helleday, T.
Source: Self-asserted source
Nasrollah saleh-gohari via Scopus - Elsevier
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