Nadia Alhashmi

1.3k total citations
15 papers, 678 citations indexed

About

Nadia Alhashmi is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Nadia Alhashmi has authored 15 papers receiving a total of 678 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Rheumatology. Recurrent topics in Nadia Alhashmi's work include Metabolism and Genetic Disorders (3 papers), Connective tissue disorders research (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Nadia Alhashmi is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Connective tissue disorders research (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Nadia Alhashmi collaborates with scholars based in Oman, Saudi Arabia and India. Nadia Alhashmi's co-authors include Mohammed Al‐Owain, Fowzan S. Alkuraya, Fathiya Al-Murshedi, Hanif Khalak, Mais Hashem, H. Alrayes, Safiya Al Abrawi, Sulaiman M. Al‐Mayouf, Reem Abdwani and Abdullah Al Sonbul and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Journal of Medical Genetics.

In The Last Decade

Nadia Alhashmi

15 papers receiving 664 citations

Peers

Nadia Alhashmi

IMMUN

RHEUM

GENET

Julia E. Maxson United States

Fathiya Al-Murshedi Oman

Hajra Tily United States

Bobby P. C. Koeleman Netherlands

Manuela Fanciulli Italy

Kristina Duvefelt Sweden

Rebeca Dieguez‐Gonzalez Spain

Arseni Markoff Germany

Xana Kim-Howard United States

Hillery F. Gray United States

Julia E. Maxson United States

Nadia Alhashmi

166 ×0.6

IMMUN

406 ×1.6

214 ×0.9

RHEUM

212 ×1.0

GENET

59 ×1.0

Citations per year, relative to Nadia Alhashmi Nadia Alhashmi (= 1×) peers Julia E. Maxson

Countries citing papers authored by Nadia Alhashmi

Since Specialization

Citations

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

Fields of papers citing papers by Nadia Alhashmi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadia Alhashmi

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Alhashmi, Nadia, et al.. (2023). LRP4 site-specific variants in the third β-propeller domain causes congenital myasthenic syndrome type 17. European Journal of Medical Genetics. 67. 104903–104903. 2 indexed citations

Ganesh, Anuradha, Nadia Alhashmi, Abeer Al‐Saegh, et al.. (2022). Further phenotypic delineation of Alazami syndrome. American Journal of Medical Genetics Part A. 188(8). 2485–2490. 4 indexed citations

Al‐Thihli, Khalid, Nadia Alhashmi, Mohammed Mohammed, et al.. (2020). Deficiency of acyl‐CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onset. Clinical Genetics. 99(3). 376–383. 5 indexed citations

Mohammed, Mohammed, et al.. (2018). Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder. European Journal of Medical Genetics. 62(11). 103583–103583. 30 indexed citations

Alhashmi, Nadia, et al.. (2018). Exome Sequencing Identifies a Novel Sorting Nexin 14 Gene Mutation Causing Cerebellar Atrophy and Intellectual Disability. SHILAP Revista de lepidopterología. 2018. 1–3. 3 indexed citations

Shanmugam, Naresh, Mettu Srinivas Reddy, Khalid Al‐Thihli, et al.. (2018). Auxiliary Partial Orthotopic Liver Transplantation for Monogenic Metabolic Liver Diseases: Single-Centre Experience. JIMD Reports. 45. 29–36. 14 indexed citations

Ben‐Omran, Tawfeg, Khushnooda Ramzan, Ruqaiah Altassan, et al.. (2018). Delineating the phenotypic spectrum of hyperphosphatasia with mental retardation syndrome 4 in 14 patients of Middle‐Eastern origin. American Journal of Medical Genetics Part A. 176(12). 2850–2857. 5 indexed citations

Al‐Thihli, Khalid, Fathiya Al-Murshedi, Nadia Alhashmi, et al.. (2014). Consanguinity, Endogamy and Inborn Errors of Metabolism in Oman: A Cross-Sectional Study. Human Heredity. 77(1-4). 183–188. 24 indexed citations

Shaheen, Ranad, Anas M. Alazami, Muneera Alshammari, et al.. (2012). Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation. Journal of Medical Genetics. 49(10). 630–635. 108 indexed citations

10.

Alhashmi, Nadia, Faiqa Imtiaz, Khushnooda Ramzan, et al.. (2012). Novel splice (IVS18+1G>C) mutation in COL2A1 causing Kniest dysplasia. Clinical Dysmorphology. 22(1). 39–41. 7 indexed citations

11.

Kaya, Namik, Hesham Aldhalaan, Banan Al‐Younes, et al.. (2011). Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(7). 826–834. 53 indexed citations

12.

Khalifa, Ola, et al.. (2011). Oral–facial–digital syndrome type 1. Clinical Dysmorphology. 21(2). 77–79. 9 indexed citations

13.

Shaheen, Ranad, Mohammed Al‐Owain, Eissa Faqeih, et al.. (2011). Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans. American Journal of Medical Genetics Part A. 155(6). 1448–1452. 55 indexed citations

14.

Al‐Mayouf, Sulaiman M., Reem Abdwani, Safiya Al Abrawi, et al.. (2011). Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus. Nature Genetics. 43(12). 1186–1188. 339 indexed citations

15.

Shuaib, Taghreed, Nadia Alhashmi, Mohammad Ghaziuddin, et al.. (2011). Propionic Acidemia Associated With Visual Hallucinations. Journal of Child Neurology. 27(6). 799–803. 20 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.

Explore authors with similar magnitude of impact