Contribution of GJB2 mutations to hearing loss in the Hazara Division of Pakistan

di Bukhari, Ihtisham, Mujtaba, Ghulam, Naz, Sadaf
Pubblicazione 2013

A p.C343S Missense Mutation in PJVK causes Progressive Hearing Loss

di Mujtaba, Ghulam, Bukhari, Ihtisham, Fatima, Amara, Naz, Sadaf
Pubblicazione 2012

Blood-testis barrier and spermatogenesis: lessons from genetically-modified mice

di Jiang, Xiao-Hua, Bukhari, Ihtisham, Zheng, Wei, Yin, Shi, Wang, Zheng, Cooke, Howard J, Shi, Qing-Hua
Pubblicazione 2014

BPA exposure is related to metabolic changes in obese Saudi children

di Al-Daghri, Nasser M, Abd-Alrahman, Sherif H, Bukhari, Ihtisham, Panigrahy, Amaresh, Khattak, Malak NK, Alokail, Majed
Pubblicato in Int J Clin Exp Pathol (2017)

A Novel APTX Variant and Ataxia with Oculomotor Apraxia Type 1

di Manzoor, Humera, Bukhari, Ihtisham, Wajid, Muhammad, Zhang, Yuanwei, Zhang, Huan, Brüggemann, Norbert, Klein, Christine, Shi, Qinghua, Naz, Sadaf
Pubblicato in J Clin Neurol (2017)

Associations of Serum Nitric Oxide with Vitamin D and Other Metabolic Factors in Apparently Healthy Adolescents

di Al-Daghri, Nasser M., Bukhari, Ihtisham, Yakout, Sobhy M., Sabico, Shaun, Khattak, Malak N. K., Aziz, Ibrahim, Alokail, Majed S.
Pubblicato in Biomed Res Int (2018)

TP53LNC-DB, the database of lncRNAs in the p53 signalling network

di Khan, Muhammad Riaz, Bukhari, Ihtisham, Khan, Ranjha, Hussain, Hafiz Muhammad Jafar, Wu, Mian, Thorne, Rick Francis, Li, Jinming, Liu, Guangzhi
Pubblicato in Database (Oxford) (2019)

Vitamin D level and its relation to muscle and fat mass in adult male Arabs

di Yakout, Sobhy M., Al-Daghri, Nasser M., Bukhari, Ihtisham, Khattak, Malak N.K., Sabico, Shaun, Alokail, Majed S., Al-Attas, Omar S.
Pubblicato in Saudi J Biol Sci (2020)

miR-214-mediated downregulation of RNF8 induces chromosomal instability in ovarian cancer cells

di Wang, Zheng, Yin, Hao, Zhang, Yuanwei, Feng, Yukun, Yan, Zhaofeng, Jiang, Xiaohua, Bukhari, Ihtisham, Iqbal, Furhan, Cooke, Howard J, Shi, Qinghua
Pubblicato in Cell Cycle (2014)

Whole-exome sequencing identifies a novel mutation in spermine synthase gene (SMS) associated with Snyder-Robinson Syndrome

di Qazi, Talal J., Wu, Qiao, Aierken, Ailikemu, Lu, Daru, Bukhari, Ihtisham, Hussain, Hafiz M. J., Yang, Jingmin, Mir, Asif, Qing, Hong
Pubblicato in BMC Med Genet (2020)

Parathyroid hormone in relation to various vitamin D metabolites in adult females

di Al-Daghri, Nasser M., Yakout, Sobhy, Bukhari, Ihtisham, Khattak, Malak N.K., Al-Saleh, Yousef, Aljohani, Naji, Al-Attas, Omar S., Alokail, Majed
Pubblicato in Medicine (Baltimore) (2017)

Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia

di Wu, Caiyun, Wang, Liu, Iqbal, Furhan, Jiang, Xiaohua, Bukhari, Ihtisham, Guo, Tonghang, Yin, Gengxin, Cooke, Howard J., Cao, Zhenyi, Jiang, Hong, Shi, Qinghua
Pubblicato in Mol Cytogenet (2016)

Association of Polymorphisms in RANK and RANKL Genes with Osteopenia in Arab Postmenopausal Women

di Abdi, Saba, Bukhari, Ihtisham, Ansari, Mohammed G. A., BinBaz, Rawan A., Mohammed, Abdul Khader, Hussain, Syed Danish, Aljohani, Naji, Al-Daghri, Nasser M.
Pubblicato in Dis Markers (2020)

Specific deficiency of Plzf paralog, Zbtb20, in Sertoli cells does not affect spermatogenesis and fertility in mice

di Jiang, Xiaohua, Zhang, Huan, Yin, Shi, Zhang, Yuanwei, Yang, Weimei, Zheng, Wei, Wang, Liu, Wang, Zheng, Bukhari, Ihtisham, Cooke, Howard J., Iqbal, Furhan, Shi, Qinghua
Pubblicato in Sci Rep (2014)

SAT-021 Efficacy of Vitamin D Supplementation According to Vitamin D Binding Protein Polymorphisms

di Al-Daghri, Nasser, Bukhari, Ihtisham, Rikli, Maryam, Abdi, Saba, Ansari, Mohammed, Abdulkhader, Mohammed, Sabico, Shaun, Hussain, Syed Danish, Alenad, Amal, Al-Saleh, Yousef, Alokail, Majed
Pubblicato in J Endocr Soc (2019)

A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf family

di Zhang, Chao, Liu, Jiaojiao, Iqbal, Furhan, Lu, Yan, Mustafa, Saima, Bukhari, Firdous, Lou, Haiyi, Fu, Ruiqing, Wu, Zhendong, Yang, Xiong, Bukhari, Ihtisham, Aslam, Muhammad, Xu, Shuhua
Pubblicato in Heredity (Edinb) (2017)

Unrepaired DNA damage facilitates elimination of uniparental chromosomes in interspecific hybrid cells

di Wang, Zheng, Yin, Hao, Lv, Lei, Feng, Yingying, Chen, Shaopeng, Liang, Junting, Huang, Yun, Jiang, Xiaohua, Jiang, Hanwei, Bukhari, Ihtisham, Wu, Lijun, Cooke, Howard J, Shi, Qinghua
Pubblicazione 2014

Genetic causes of moderate to severe hearing loss point to modifiers

di Naz, Sadaf, Imtiaz, Ayesha, Mujtaba, Ghulam, Maqsood, Azra, Bashir, Rasheeda, Bukhari, Ihtisham, Khan, Muhammad R., Ramzan, Memoona, Fatima, Amara, Rehman, Atteeq U., Iqbal, Muddassar, Chaudhry, Taimur, Lund, Merete, Brewer, Carmen C., Morell, Robert J., Friedman, Thomas B.
Pubblicato in Clin Genet (2016)

Correction: A homozygous FANCM frameshift pathogenic variant causes male infertility

di Yin, Hao, Ma, Hui, Hussain, Sajjad, Zhang, Huan, Xie, Xuefeng, Jiang, Long, Jiang, Xiaohua, Iqbal, Furhan, Bukhari, Ihtisham, Jiang, Hanwei, Ali, Asim, Zhong, Liangwen, Li, Tao, Fan, Suixing, Zhang, Beibei, Gao, Jianing, Li, Yang, Nazish, Jabeen, Khan, Teka, Khan, Manan, Zubair, Muhammad, Hao, Qiaomei, Fang, Hui, Huang, Jun, Huleihel, Mahmoud, Sha, Jiahao, Pandita, Tej K., Zhang, Yuanwei, Shi, Qinghua
Pubblicato in Genet Med (2018)

A homozygous FANCM frameshift pathogenic variant causes male infertility

di Yin, Hao, Ma, Hui, Hussain, Sajjad, Zhang, Huan, Xie, Xuefeng, Jiang, Long, Jiang, Xiaohua, Iqbal, Furhan, Bukhari, Ihtisham, Jiang, Hanwei, Ali, Asim, Zhong, Liangwen, Li, Tao, Fan, Suixing, Zhang, Beibei, Gao, Jianing, Li, Yang, Nazish, Jabeen, Khan, Teka, Khan, Manan, Zubair, Muhammad, Hao, Qiaomei, Fang, Hui, Huang, Jun, Huleihel, Mahmoud, Sha, Jiahao, Pandita, Tej K., Zhang, Yuanwei, Shi, Qinghua
Pubblicato in Genet Med (2018)