Kimia Kahrizi
Kimia Kahrizi
Genetics Research Center, University of Social Welfare and Rehabilitation Sciences
No verified email
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Cited by
Cited by
Year
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
H Najmabadi, H Hu, M Garshasbi, T Zemojtel, SS Abedini, W Chen, ...
Nature 478 (7367), 57-63, 2011
7002011
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation
MM Motazacker, BR Rost, T Hucho, M Garshasbi, K Kahrizi, R Ullmann, ...
The American Journal of Human Genetics 81 (4), 792-798, 2007
1892007
Human male infertility caused by mutations in the CATSPER1 channel protein
MR Avenarius, MS Hildebrand, Y Zhang, NC Meyer, LLH Smith, K Kahrizi, ...
The American Journal of Human Genetics 84 (4), 505-510, 2009
1832009
Mutations in NSUN2 cause autosomal-recessive intellectual disability
L Abbasi-Moheb, S Mertel, M Gonsior, L Nouri-Vahid, K Kahrizi, S Cirak, ...
The American Journal of Human Genetics 90 (5), 847-855, 2012
1692012
A defect in the TUSC3 gene is associated with autosomal recessive mental retardation
M Garshasbi, V Hadavi, H Habibi, K Kahrizi, R Kariminejad, F Behjati, ...
The American Journal of Human Genetics 82 (5), 1158-1164, 2008
1662008
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci
H Najmabadi, MM Motazacker, M Garshasbi, K Kahrizi, A Tzschach, ...
Human genetics 121 (1), 43-48, 2007
1482007
Identification of mutations in TRAPPC9, which encodes the NIK-and IKK-β-binding protein, in nonsyndromic autosomal-recessive mental retardation
A Mir, L Kaufman, A Noor, MM Motazacker, T Jamil, M Azam, K Kahrizi, ...
The American Journal of Human Genetics 85 (6), 909-915, 2009
1362009
Genetic male infertility and mutation of CATSPER ion channels
MS Hildebrand, MR Avenarius, M Fellous, Y Zhang, NC Meyer, J Auer, ...
European Journal of Human Genetics 18 (11), 1178-1184, 2010
1242010
GJB2 mutations: Passage through Iran
H Najmabadi, C Nishimura, K Kahrizi, Y Riazalhosseini, M Malekpour, ...
American Journal of Medical Genetics Part A 133 (2), 132-137, 2005
1202005
Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants
AE Shearer, RW Eppsteiner, KT Booth, SS Ephraim, J Gurrola II, ...
The American Journal of Human Genetics 95 (4), 445-453, 2014
1192014
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42
G Borck, AU Rehman, K Lee, HM Pogoda, N Kakar, S Von Ameln, ...
The American Journal of Human Genetics 88 (2), 127-137, 2011
1022011
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans
N Grillet, M Schwander, MS Hildebrand, A Sczaniecka, A Kolatkar, ...
The American Journal of Human Genetics 85 (3), 328-337, 2009
1022009
Sensorineural deafness and male infertility: a contiguous gene deletion syndrome
Y Zhang, M Malekpour, N Al-Madani, K Kahrizi, M Zanganeh, M Mohseni, ...
Journal of medical genetics 44 (4), 233-240, 2007
942007
GJB2 mutations in Iranians with autosomal recessive non‐syndromic sensorineural hearing loss
H Najmabadi, RA Cucci, S Sahebjam, N Kouchakian, M Farhadi, ...
Human mutation 19 (5), 572-572, 2002
922002
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly
M Garshasbi, MM Motazacker, K Kahrizi, F Behjati, SS Abedini, SE Nieh, ...
Human genetics 118 (6), 708-715, 2006
902006
A clinical and molecular genetic study of 112 Iranian families with primary microcephaly
H Darvish, S Esmaeeli-Nieh, GB Monajemi, M Mohseni, ...
Journal of medical genetics 47 (12), 823-828, 2010
872010
ST3GAL3 mutations impair the development of higher cognitive functions
H Hu, K Eggers, W Chen, M Garshasbi, MM Motazacker, K Wrogemann, ...
The American Journal of Human Genetics 89 (3), 407-414, 2011
852011
Mutations in the alpha 1, 2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability
MA Rafiq, AW Kuss, L Puettmann, A Noor, A Ramiah, G Ali, H Hu, ...
The American Journal of Human Genetics 89 (1), 176-182, 2011
802011
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus
W Chen, K Kahrizi, NC Meyer, Y Riazalhosseini, G Van Camp, ...
Journal of medical genetics 42 (10), e61-e61, 2005
782005
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots
AW Kuss, M Garshasbi, K Kahrizi, A Tzschach, F Behjati, H Darvish, ...
Human genetics 129 (2), 141-148, 2011
712011
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