Faiqa Imtiaz

2.1k total citations
74 papers, 1.1k citations indexed

About

Faiqa Imtiaz is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Faiqa Imtiaz has authored 74 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 24 papers in Genetics and 14 papers in Clinical Biochemistry. Recurrent topics in Faiqa Imtiaz's work include Metabolism and Genetic Disorders (14 papers), Hearing, Cochlea, Tinnitus, Genetics (9 papers) and Mitochondrial Function and Pathology (7 papers). Faiqa Imtiaz is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Hearing, Cochlea, Tinnitus, Genetics (9 papers) and Mitochondrial Function and Pathology (7 papers). Faiqa Imtiaz collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Faiqa Imtiaz's co-authors include Khushnooda Ramzan, Brian F. Meyer, Mohammed Al‐Owain, Moeenaldeen AlSayed, J. Jay Gargus, Bryan Winchester, Zuhair N. Al‐Hassnan, Hamad Alzaidan, Hudson H. Freeze and Gert Matthijs and has published in prestigious journals such as SHILAP Revista de lepidopterología, Diabetes Care and Gene.

In The Last Decade

Faiqa Imtiaz

70 papers receiving 1.0k citations

Peers

Countries citing papers authored by Faiqa Imtiaz

Since Specialization

Citations

This map shows the geographic impact of Faiqa Imtiaz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Faiqa Imtiaz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Faiqa Imtiaz more than expected).

Fields of papers citing papers by Faiqa Imtiaz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Faiqa Imtiaz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Faiqa Imtiaz. The network helps show where Faiqa Imtiaz may publish in the future.

Co-authorship network of co-authors of Faiqa Imtiaz

This figure shows the co-authorship network connecting the top 25 collaborators of Faiqa Imtiaz. A scholar is included among the top collaborators of Faiqa Imtiaz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Faiqa Imtiaz. Faiqa Imtiaz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Clinical and molecular characterization of familial chylomicronemia in Saudi patients: a retrospective study 2024 ·Frontiers in Endocrinology ·Abdullah Al‐Ashwal, (unknown), Afaf Alsagheir, (unknown), Khushnooda Ramzan, Faiqa Imtiaz, (unknown)	1
2	Long-term treatment for Laron syndrome with IGF-1 injection over 22 years in Saudi: A cohort study 2024 ·Hormone Research in Paediatrics ·Abdullah Al‐Ashwal, (unknown), Khushnooda Ramzan, Faiqa Imtiaz, (unknown)	1
3	Wild-type S100A3 and S100A13 restore calcium homeostasis and mitigate mitochondrial dysregulation in pulmonary fibrosis patient-derived cells 2023 ·Frontiers in Cell and Developmental Biology ·(unknown), (unknown), Mohammed Khalid, (unknown), Maher Al‐Saif, Faiqa Imtiaz, Khushnooda Ramzan, (unknown), Ayodele Alaiya, Brian F. Meyer, Sergei P. Atamas, Kate S. Collison, Khalid S.A. Khabar, Jeffrey D. Hasday, Futwan Al‐Mohanna	2
4	Genetic basis of pulmonary arterial hypertension: a prospective study from a highly inbred population 2021 ·Pulmonary Circulation ·Abdullah M. Aldalaan, Khushnooda Ramzan, Sarfraz Saleemi, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mohammed Al‐Owain, Faiqa Imtiaz	0
5	Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss 2020 ·Genes ·Khushnooda Ramzan, Nouf S. Al‐Numair, (unknown), (unknown), Nadia Sakati, Selwa A.F. Al-Hazzaa, Mohammed Al‐Owain, Faiqa Imtiaz	12
6	Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia 2019 ·Molecular Genetics and Metabolism Reports ·Mohamed H. Al‐Hamed, Faiqa Imtiaz, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Hamad Alzaidan, Mohamed Al‐Amoudi, Eissa Faqeih, Majid Alfadhel, Ali Alasmari, Mohammed M. Saleh, Fuad Al Mutairi, Nabil Moghrabi, Moeenaldeen AlSayed	12
7	A retrospective biochemical, molecular, and neurocognitive review of Saudi patients with argininosuccinic aciduria 2018 ·European Journal of Medical Genetics ·Ruqaiah Altassan, Dalal Bubshait, Faiqa Imtiaz, Zuhair Rahbeeni	4
8	Genetic characterization of Usher syndrome in Saudi Arabia population 2017 ·Journal of Molecular and Genetic Medicine ·(unknown), Faiqa Imtiaz	1
9	Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden 2016 ·Genetics in Medicine ·Mohamed Abouelhoda, (unknown), Mohamed El-Kalioby, Nisha Patel, Hanan E. Shamseldin, Dorota Monies, Nada Al Tassan, Khushnooda Ramzan, Faiqa Imtiaz, Ranad Shaheen, Fowzan S. Alkuraya	67
10	Clinical and Molecular Characterization of 25-Hydroxylase Deficiency in Saudi Patients 2016 ·Faiqa Imtiaz, (unknown), (unknown), Abdulrahman A. Alrajhi	1
11	Tracheobronchial anomalies in a patient with Schimke immuno‐osseous dysplasia (SIOD) 2014 ·American Journal of Medical Genetics Part A ·Abdullah F. Mobeireek, Sarfraz Saleemi, Mohammad Khalid, Faiqa Imtiaz, (unknown)	1
12	Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia 2014 ·JIMD Reports ·Faiqa Imtiaz, (unknown), (unknown), Mohamed H. Al‐Hamed, (unknown), Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Hamad Alzaidan, Zuhair Rahbeeni, Alya Qari, Eissa Faqeih, Ali Alasmari, (unknown), Majid Alfadhel, Wafaa Eyaid, Mohamed S. Rashed, Moeenaldeen AlSayed	5
13	Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family 2013 ·Gene ·Khushnooda Ramzan, Mohammed Al‐Owain, (unknown), (unknown), (unknown), (unknown), Faiqa Imtiaz	18
14	A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene: Figure 1 2012 ·Journal of Medical Genetics ·Ola Khalifa, Faiqa Imtiaz, (unknown), Zuhair N. Al‐Hassnan, Amal Al‐Hemidan, (unknown), (unknown), (unknown), Nadia Sakati, James Hyland, Mohammed Al‐Owain	14
15	Smith–Lemli–Opitz syndrome among Arabs 2011 ·Clinical Genetics ·Mohammad Al-Owain, Faiqa Imtiaz, Taghreed Shuaib, Amr Edrees, (unknown), Nadia Sakati, Zuhair N. Al‐Hassnan, (unknown), Zuhair Rahbeeni, Seham Alameer, Eissa Faqeih, (unknown), Amal Alhashem, (unknown), Ahmad Alodaib, (unknown), (unknown)	8
16	Reliable prenatal diagnosis of Canavan disease by measuring N‐acetylaspartate in amniotic fluid using liquid chromatography tandem mass spectrometry 2009 ·Prenatal Diagnosis ·(unknown), Wesam Kurdi, Faiqa Imtiaz, (unknown), (unknown), Maha Tulbah, Maha Alnemer, Mohamed S. Rashed	8
17	Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease 2008 ·Genetics in Medicine ·Namik Kaya, Faiqa Imtiaz, Dilek Çolak, Moeenaldeen AlSayed, Ali Al‐Odaib, (unknown), Bashayer Al‐Mubarak, Mohammad Al-Owain, Hesham Aldhalaan, Aziza Chedrawi, Zuhair N. Al‐Hassnan, Serdar Coşkun, Nadia Sakati, Pinar T. Ozand, Brian F. Meyer	17
18	Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population 2006 ·BMC Medical Genetics ·Moeenaldeen AlSayed, Faiqa Imtiaz, Osama Alsmadi, (unknown), Brian F. Meyer	14
19	Successful treatment with oral mannose of a patient with congenital disorder of glycosylation Ib (CDG Ib) 2000 ·Glycobiology ·Christian J. Hendriksz, Paula L. McClean, (unknown), Geoffrey Keir, (unknown), Faiqa Imtiaz, Els Schollen, Gert Matthijs, Bryan Winchester	4
20	Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia) 2000 ·Human Mutation ·Gert Matthijs, Els Schollen, Cecilia Bjursell, Anna Erlandson, Hudson H. Freeze, Faiqa Imtiaz, Søren K. Kjærgaard, Tommy Martinsson, M. Schwartz, Nathalie Séta, Sandrine Vuillaumier‐Barrot, Vibeke Westphal, Bryan Winchester	122

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