Nadia Sakati

2.9k total citations
78 papers, 1.7k citations indexed

About

Nadia Sakati is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Nadia Sakati has authored 78 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 27 papers in Genetics and 20 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Nadia Sakati's work include Metabolism and Genetic Disorders (13 papers), Diabetes Management and Research (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Nadia Sakati is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Diabetes Management and Research (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Nadia Sakati collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Nadia Sakati's co-authors include Nicholas Woodhouse, R D Milner, Arne Ohlsson, Pinar T. Ozand, Abdullah Al‐Ashwal, Joy D. Cogan, William L. Nyhan, Sami A. Sanjad, Bassam Bin‐Abbas and William S. Sly and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

In The Last Decade

Nadia Sakati

78 papers receiving 1.6k citations

Peers

Countries citing papers authored by Nadia Sakati

Since Specialization

Citations

This map shows the geographic impact of Nadia Sakati'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 Nadia Sakati with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nadia Sakati more than expected).

Fields of papers citing papers by Nadia Sakati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nadia Sakati. 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 Nadia Sakati. The network helps show where Nadia Sakati may publish in the future.

Co-authorship network of co-authors of Nadia Sakati

This figure shows the co-authorship network connecting the top 25 collaborators of Nadia Sakati. A scholar is included among the top collaborators of Nadia Sakati 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 Nadia Sakati. Nadia Sakati 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	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
2	Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype 2017 ·American Journal of Medical Genetics Part A ·Ruqaiah Altassan, (unknown), Tariq Masoodi, (unknown), Ola Khalifa, Hamad Alzaidan, Nadia Sakati, (unknown), Zuhair N. Al‐Hassnan, Yousef Binamer, (unknown), William J. Wade, Zayed Al‐Zayed, (unknown), (unknown), Brian F. Meyer, (unknown), Salma M. Wakil	15
3	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
4	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
5	FKBP10 and Bruck Syndrome: Phenotypic Heterogeneity or Call for Reclassification? 2010 ·The American Journal of Human Genetics ·Ranad Shaheen, Mohammed Al‐Owain, Nadia Sakati, Zayed Al‐Zayed, Fowzan S. Alkuraya	5
6	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
7	Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome 2008 ·The American Journal of Human Genetics ·Anas M. Alazami, Amr Al‐Saif, Abdulaziz Alsemari, Saeed Bohlega, Soumaya Zlitni, Fatema Alzahrani, Prashant Bavi, Namik Kaya, Dilek Çolak, Hanif Khalak, (unknown), Borut Peterlin, Sumita Danda, Kailash P. Bhatia, Susanne A. Schneider, Nadia Sakati, Christopher A. Walsh, Futwan Al‐Mohanna, Brian F. Meyer, Fowzan S. Alkuraya	94
8	Comparison of Insulin Pump and Multiple Daily Injection Regimens in Type 1 Diabetic Patients 2006 ·Current Pediatric Research ·Bassam Bin‐Abbas, (unknown), Nadia Sakati, Abdullah Al‐Ashwal	1
9	Persistent Hyperinsulinaemic Hypoglycaemia of Infancy in 43 Children: Long-term Clinical and Surgical Follow-up 2006 ·Asian Journal of Surgery ·(unknown), Nadia Sakati, Abdullah Al‐Ashwal, Bassam Bin‐Abbas	19
10	Mutation of a tubulin folding gene, TCFE, causes the autosomal recessive Kenny-Caffey syndrome 2002 ·Journal of Investigative Medicine ·George A. Díaz, Bruce D. Gelb, (unknown), Marios Kambouris, Nadia Sakati, Eli Hershkovitz, Ruti Parvari	1
11	Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency 1999 ·Clinical Genetics ·(unknown), (unknown), (unknown), Mohammed Alessa, (unknown), Nadia Sakati, Sami A. Sanjad, (unknown), Marios Kambouris	27
12	Hyperinsulinism and hyperammonaemia 1998 ·Journal of Inherited Metabolic Disease ·(unknown), Mohammed Alessa, Abbas Al Mutair, (unknown), Nadia Sakati, Pinar T. Ozand	2
13	Four Contiguous Amino Acid Substitutions, Identified in Patients with Laron Syndrome, Differently Affect the Binding Affinity and Intracellular Trafficking of the Growth Hormone Receptor¹ 1998 ·The Journal of Clinical Endocrinology & Metabolism ·Jérôme Wojcik, Mary Anne Berg, Nazario Esposito, Mitchell E. Geffner, Nadia Sakati, Edward O. Reiter, Steven Dower, Uta Francke, Marie-Catherine Postel-Vinay, J Finidori	39
14	A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literature 1997 ·American Journal of Medical Genetics ·M. Anwar Iqbal, (unknown), David Wu, Nadia Sakati	7
15	Osteodysplastic variant of primordial dwarfism 1991 ·American Journal of Medical Genetics ·(unknown), C. Hugosson, Nadia Sakati, William L. Nyhan	11
16	Concurrence of robinow syndrome and Crigler‐Najar syndrome in two offspring of first cousins 1990 ·American Journal of Medical Genetics ·Hisham M. Nazer, Thirumazhisai S. Gunasekaran, Nadia Sakati, William L. Nyhan	11
17	Cystic fibrosis in Saudi Arabia 1989 ·European Journal of Pediatrics ·Hisham M. Nazer, (unknown), Nadia Sakati, Rishi Philip Mathew, (unknown), (unknown)	29
18	Pituitary Gland Enlargement in Primary Hypothyroidism: A Report of 5 Cases with Follow-Up Data 1989 ·Hormone Research ·Mohammed Ahmed, M. Banna, Nadia Sakati, (unknown)	26
19	Hereditary Resistance to 1,25-Dihydroxyvitamin D: Clinical and Radiological Improvement during High-Dose Oral Calcium Therapy 1986 ·Hormone Research ·Nadia Sakati, Nicholas Woodhouse, (unknown), (unknown), (unknown), Stephen J. Marx	23
20	Johanson‐Blizzard syndrome in a large inbred kindred with three involved members 1978 ·Clinical Genetics ·(unknown), (unknown), Nadia Sakati, William L. Nyhan	26

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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