Nouriya Al‐Sannaa

2.2k total citations
27 papers, 611 citations indexed

About

Nouriya Al‐Sannaa is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Nouriya Al‐Sannaa has authored 27 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 8 papers in Physiology. Recurrent topics in Nouriya Al‐Sannaa's work include Lysosomal Storage Disorders Research (7 papers), Metabolism and Genetic Disorders (6 papers) and Genetic Syndromes and Imprinting (5 papers). Nouriya Al‐Sannaa is often cited by papers focused on Lysosomal Storage Disorders Research (7 papers), Metabolism and Genetic Disorders (6 papers) and Genetic Syndromes and Imprinting (5 papers). Nouriya Al‐Sannaa collaborates with scholars based in Saudi Arabia, United States and Germany. Nouriya Al‐Sannaa's co-authors include Ahmad S. Teebi, Sultan Al‐Khenaizan, Revi P. Mathew, Mathew Cherian, Ian Adatia, Ahmed M. Alkhunaizi, Millan S. Patel, David Chitayat, Derek G. Human and M. E. Suzanne Lewis and has published in prestigious journals such as Nature Communications, The American Journal of Human Genetics and Journal of Pediatric Surgery.

In The Last Decade

Nouriya Al‐Sannaa

27 papers receiving 593 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Nouriya Al‐Sannaa Saudi Arabia 13 290 154 150 99 96 27 611
Orna Staretz‐Chacham Israel 14 227 0.8× 165 1.1× 114 0.8× 61 0.6× 83 0.9× 38 617
Moeenaldeen AlSayed Saudi Arabia 15 254 0.9× 333 2.2× 183 1.2× 130 1.3× 86 0.9× 49 737
Hamad Alzaidan Saudi Arabia 14 283 1.0× 55 0.4× 173 1.2× 65 0.7× 132 1.4× 39 578
Lock Hock Ngu Malaysia 18 503 1.7× 181 1.2× 242 1.6× 113 1.1× 299 3.1× 59 899
Argirios Dinopoulos Greece 14 410 1.4× 349 2.3× 111 0.7× 40 0.4× 142 1.5× 43 998
F. A. Beemer Netherlands 12 232 0.8× 293 1.9× 167 1.1× 248 2.5× 106 1.1× 21 714
Siddharth Banka United Kingdom 18 339 1.2× 111 0.7× 480 3.2× 105 1.1× 85 0.9× 55 991
Peter Huppke Germany 20 177 0.6× 116 0.8× 66 0.4× 218 2.2× 66 0.7× 39 1.1k
Esmée Oussoren Netherlands 15 245 0.8× 383 2.5× 106 0.7× 166 1.7× 89 0.9× 32 768
Guilhem Solé France 15 250 0.9× 119 0.8× 82 0.5× 107 1.1× 25 0.3× 62 731

Countries citing papers authored by Nouriya Al‐Sannaa

Since Specialization
Citations

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

Fields of papers citing papers by Nouriya Al‐Sannaa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nouriya Al‐Sannaa. 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 Nouriya Al‐Sannaa. The network helps show where Nouriya Al‐Sannaa may publish in the future.

Co-authorship network of co-authors of Nouriya Al‐Sannaa

This figure shows the co-authorship network connecting the top 25 collaborators of Nouriya Al‐Sannaa. A scholar is included among the top collaborators of Nouriya Al‐Sannaa 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 Nouriya Al‐Sannaa. Nouriya Al‐Sannaa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
AlSayed, Moeenaldeen, et al.. (2024). Consensus-based expert recommendations on the management of MPS IVa and VI in Saudi Arabia. Orphanet Journal of Rare Diseases. 19(1). 269–269. 2 indexed citations
2.
Bertoli‐Avella, Aida M., José María García-Aznar, Oliver Brandau, et al.. (2018). Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability. European Journal of Human Genetics. 26(4). 592–598. 17 indexed citations
3.
Alkhunaizi, Ahmed M. & Nouriya Al‐Sannaa. (2017). Renal Involvement in Methylmalonic Aciduria. Kidney International Reports. 2(5). 956–960. 10 indexed citations
4.
Bréchet, Aline, Rebecca Buchert, Jochen Schwenk, et al.. (2017). AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability. Nature Communications. 8(1). 15910–15910. 56 indexed citations
5.
Al‐Sannaa, Nouriya, Deborah Barbouth, Cyril Goizet, et al.. (2015). Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships. Orphanet Journal of Rare Diseases. 10(1). 131–131. 60 indexed citations
6.
Al‐Sannaa, Nouriya, et al.. (2015). Nail-Patella Syndrome. Journal of Cutaneous Medicine and Surgery. 19(6). 595–599. 2 indexed citations
7.
Jasmi, Fatma Al, Mohammed Al Jumah, Nouriya Al‐Sannaa, et al.. (2015). Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group. BMC Neurology. 15(1). 205–205. 26 indexed citations
8.
Kirwin, Susan M., et al.. (2013). A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA. Molecular Genetics & Genomic Medicine. 1(2). 113–117. 13 indexed citations
9.
Twigg, Stephen R.F., Dagan Jenkins, C.D.O. Cooper, et al.. (2012). Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization. The American Journal of Human Genetics. 91(5). 897–905. 56 indexed citations
10.
Alkhunaizi, Ahmed M., Nouriya Al‐Sannaa, & Wasim F. Raslan. (2011). Hyperoxaluria and Rapid Development of Renal Failure Following a Combined Liver and Kidney Transplantation: Emphasis on Sequential Transplantation. JIMD Reports. 3. 91–95. 11 indexed citations
11.
Mathew, Revi P., et al.. (2010). Incidence and patterns of inborn errors of metabolism in the Eastern Province of Saudi Arabia, 1983-2008. Annals of Saudi Medicine. 30(4). 271–277. 89 indexed citations
12.
Al‐Sannaa, Nouriya, et al.. (2010). Carnitine-acylcarnitine translocase deficiency. Clinical course of three Saudi children with a severe phenotype.. PubMed. 31(8). 931–4. 8 indexed citations
13.
Cherian, Mathew & Nouriya Al‐Sannaa. (2009). Clinical spectrum of Bardet–Biedl syndrome among four Saudi Arabian families. Clinical Dysmorphology. 18(4). 188–194. 17 indexed citations
14.
Cherian, Mathew, et al.. (2008). Hirschsprung's disease in Arab siblings with Bardet-Biedl syndrome. Journal of Pediatric Surgery. 43(6). 1213–1217. 6 indexed citations
15.
Seliem, Mohamed A., et al.. (2006). Influence of Consanguinity on the Pattern of Familial Aggregation of Congenital Cardiovascular Anomalies in an Outpatient Population. Public Health Genomics. 10(1). 27–31. 13 indexed citations
16.
Al‐Sannaa, Nouriya, et al.. (2005). Dihydropyrimidine dehydrogenase deficiency presenting at birth. Journal of Inherited Metabolic Disease. 28(5). 793–796. 14 indexed citations
17.
Patel, Millan S., Glenn Taylor, Nouriya Al‐Sannaa, et al.. (2004). Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams–Oliver syndrome. American Journal of Medical Genetics Part A. 129A(3). 294–299. 61 indexed citations
18.
Al‐Khenaizan, Sultan, Nouriya Al‐Sannaa, & Ahmad S. Teebi. (2001). Chondroectodermal Dysplasia –The Ellis‐van Creveld Syndrome. Pediatric Dermatology. 18(1). 68–70. 91 indexed citations
19.
20.
Al‐Sannaa, Nouriya, Ian Adatia, & Ahmad S. Teebi. (2000). Transverse limb defects associated with aorto-pulmonary vascular abnormalities: Vascular disruption sequence or atypical presentation of Adams-Oliver syndrome?. American Journal of Medical Genetics. 94(5). 400–404. 10 indexed citations

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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