Mais Hashem

5.5k citations

51 papers · 1.8k indexed · h-index 23

Impact in

Ophthalmology top 2%
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in

Genetics 30
- Genomics and Rare Diseases 12
- Genetics and Neurodevelopmental Disorders 6
- Connective tissue disorders research 5
- Genetic Associations and Epidemiology 5
- Genomic variations and chromosomal abnormalities 5
Clinical Biochemistry 6
- Metabolism and Genetic Disorders 6

Co-authors: Fowzan S. Alkuraya Hanan E. Shamseldin Mohammed A. Aldahmesh Mohammed Al‐Owain Niema Ibrahim Eissa Faqeih Ranad Shaheen Tarfa Al‐Sheddi
Journals: Human Genetics (9 papers)The American Journal of Human Genetics (5 papers)Genetics in Medicine (4 papers)Clinical Genetics (4 papers)Journal of Medical Genetics (2 papers)
Partner nations: Saudi Arabia United States Egypt

In The Last Decade

Mais Hashem

50 papers receiving 1.7k citations

Peers

Countries citing papers authored by Mais Hashem

Since Specialization

Citations

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

Fields of papers citing papers by Mais Hashem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Mais Hashem, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mais Hashem Line = papers co-authored together Mais Hashem links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Further delineation of the phenotypic and metabolomic profile of ALDH1L2‐related neurodevelopmental disorder Clinical Genetics ·Mikyoung You, Hanan E. Shamseldin, Dohyeon Lee, Blake R. Rushing, Gerhard Reiter, Amal Jaafar, Mais Hashem, Firdous Abdulwahab, Anas M. Abdel Rahman, Natalia I. Krupenko, Fowzan S. Alkuraya, Sergey A. Krupenko	2024	1
2	Human ‘knockouts’ of CSF3 display severe congenital neutropenia British Journal of Haematology ·J. Fernández, Dana Marafi, Kurt Salecker, D A Krasnov, Bradley St Croix, Mais Hashem, Firdous Abdulwahab, Amal Jaafar, Tarfa Alshidi, Lena Sabidussi, Ali Awaji, Fowzan S. Alkuraya	2023	3
3	Clinical utility of polygenic scores for cardiometabolic disease in Arabs Nature Communications ·Injeong Shim, Hiroyuki Kuwahara, Sampath Gnanarathne, Mais Hashem, Lama AlAbdi, Mohamed Abouelhoda, Hong‐Hee Won, Pradeep Natarajan, Patrick T. Ellinor, Amit V. Khera, Xin Gao, Fowzan S. Alkuraya, Akl C. Fahed	2023	5
4	Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders Journal of Clinical Investigation ·Huilun Wang, Olga Iglesias Das Neves, Villamar Vera, Xiaoqiong Wei, 李建新, Gerarda Cappuccio, Mais Hashem, Laurence Hubert, Arnold Münnich, Mashael Alqahtani, Qi Pang, Margit Burmeister, You Lu, Karine Poirier, Claude Besmond, Shengyi Sun, Nicola Brunetti‐Pierri, Fowzan S. Alkuraya, Ling Qi	2023	16
5	Mitochondrial “dysmorphology” in variant classification Human Genetics ·Hanan E. Shamseldin, Amal Alhashem, Brahim Tabarki, Firdous Abdulwahab, Mais Hashem, Rachid Sougrat, Fowzan S. Alkuraya	2021	3
6	An exome-first approach to aid in the diagnosis of primary ciliary dyskinesia Human Genetics ·Hanan E. Shamseldin, McLean Fw, Cricket Keating, J Francisco, P Schoenlaub, Muslim M. Alsaadi, Pierre Lamandé, Amal Alhashem, Latifatin Asmaul Chusnah, Waleed S. Ameen, Niema Ibrahim, Jason Yang, Firdous Abdulwahab, Mais Hashem, Raghu R. Chivukula, Fowzan S. Alkuraya	2020	16
7	Further delineation of MYO18B‐related autosomal recessive Klippel‐Feil syndrome with myopathy and facial dysmorphism American Journal of Medical Genetics Part A ·Steevart V Durairaj, Chad Haldeman‐Englert, Edward Cupler, X. Y. Wang, Hamad Alzaidan, Mais Hashem, Fowzan S. Alkuraya	2020	2
8	A genomics approach to females with infertility and recurrent pregnancy loss Human Genetics ·Sateesh Maddirevula, Khalid Awartani, Serdar Coşkun, Paosiyah Weaaryee, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Saad S. M. Hassan, Fowzan S. Alkuraya	2020	58
9	Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies Nature Medicine ·Gökhan Ünlü, Anja Lenaerts, Eric R. Gamazon, D. Melville, Nisha Patel, R. Sazonov, Mais Hashem, Abdullah Alfaifi, Rui Chen, Bingshan Li, Nancy J. Cox, Fowzan S. Alkuraya, Ela W. Knapik	2020	30
10	Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2 Annals of Clinical and Translational Neurology ·Patrick R. Blackburn, Matthew Schultz, 孔祥科, Dong Li, Elizabeth Bhoj, Yun Sheng Chung, Deborah L. Renaud, 关思静, Niema Ibrahim, Mais Hashem, Mohammed Zain Seidahmed, Linda Hasadsri, Samantha A. Schrier Vergano, Fowzan S. Alkuraya, Brendan C. Lanpher	2020	5
11	MDH1 deficiency is a metabolic disorder of the malate–aspartate shuttle associated with early onset severe encephalopathy Human Genetics ·Cruse Romain, Hanan E. Shamseldin, Amal Alhashem, Mais Hashem, Firdous Abdulwahab, محمد ابراهیم رزاقی, Eduard Kashuba, Fried Zwartkruis, Rene Schnell, Sabine A. Fuchs, Nanda M. Verhoeven‐Duif, Judith Jans, Fowzan S. Alkuraya	2019	40
12	Congenital glaucoma and CYP1B1: an old story revisited Human Genetics ·Hessa S. Alsaif, Arif O. Khan, Nisha Patel, Hisham Alkuraya, Mais Hashem, Firdous Abdulwahab, Niema Ibrahim, Mohammed A. Aldahmesh, Fowzan S. Alkuraya	2018	23
13	Warsaw breakage syndrome: Further clinical and genetic delineation American Journal of Medical Genetics Part A ·Ebba Alkhunaizi, Ranad Shaheen, Sanjay Kumar Bharti, Ольга Шкуренко, Karen Chong, Ghada M. H. Abdel‐Salam, Mohammed Al‐Owain, Susan Blasér, Blake C. Papsin, Mort Shuman, Mais Hashem, Nicole Martin, Meriyem Hussain, Robert M. Brosh, Fowzan S. Alkuraya, David Chitayat	2018	16
14	Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy Journal of Neurology and Neuroscience ·Wafaa S. Ramadan, Nisha Patel, Shamsa Anazi, Amal Y. Kentab, Fahad A. Bashiri, Muddathir H. Hamad, Felix R Njui, Mustafa A. Salih, Hessa S. Alsaif, Mais Hashem, Eissa Faqeih, B. Poutrel, Fowzan S. Alkuraya	2018	4
15	WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome Clinical Genetics ·Jehan Suleiman, Diane Allingham‐Hawkins, Mais Hashem, Hanan E. Shamseldin, Fowzan S. Alkuraya, Ayman W. El‐Hattab	2017	30
16	Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy Clinical Genetics ·M Kuba, Nisha Patel, Shams Anazi, Amal Y. Kentab, Fahad A. Bashiri, Muddathir H. Hamad, Jane Finegan Bartlett, Mustafa A. Salih, Hessa S. Alsaif, Mais Hashem, Eissa Faqeih, B. Poutrel, Fowzan S. Alkuraya	2017	38
17	Novel copy number variants and major limb reduction malformation: Report of three cases American Journal of Medical Genetics Part A ·Hanan E. Shamseldin, Shams Anazi, Salma M. Wakil, Eissa Faqeih, Heba Y. El Khashab, Mustafa A. Salih, Mohammad M. Al‐Qattan, Mais Hashem, M. Kaku, Fowzan S. Alkuraya	2016	8
18	A lethal phenotype associated with tissue plasminogen deficiency in humans Human Genetics ·Hanan E. Shamseldin, Abdulrahman Aldeeri, Guo Wentao, Abdulrahman Alsultan, Mais Hashem, Fowzan S. Alkuraya	2016	1
19	Exome-based case–control association study using extreme phenotype design reveals novel candidates with protective effect in diabetic retinopathy Human Genetics ·Corina Shtir, Mohammed A. Aldahmesh, Saad Al-Dahmash, Emad B. Abboud, Hisham Alkuraya, Marwan A. Abouammoh, Xiuxiu Han, Lucila Erbes, Holly Brabazon, Banan Al‐Younes, McCartney Michael L., V. I. Dilhani, Kerly Lizbeth Hidalgo Medina, Chunnan Zhang, Mais Hashem, Mohamed Abouelhoda, Dorota Monies, Fowzan S. Alkuraya	2015	35
20	AB168. Novel DYM compound heterozygous mutations in a Malaysian boy with Dyggve-Melchior-Clausen syndrome Annals of Translational Medicine ·Winnie Ong, W. Untze, 赵禄芹, 孝尚田中, Ugahara Bin Mahyuddin Yunus, Lock Hock Ngu, Nisha Patel, Mais Hashem, Fowzan S. Alkuraya, Wee Teik Keng	2015	1

About Mais Hashem

Mais Hashem is a scholar working on Genetics, Clinical Biochemistry, Molecular Biology, Ophthalmology and Immunology and Allergy, having authored 51 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Connective tissue disorders research (5 papers), Genetic Associations and Epidemiology (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and RNA Research and Splicing (5 papers). The work is most often cited by research in Ophthalmology (192 citations), Clinical Biochemistry (135 citations), Genetics (544 citations), Immunology (336 citations) and Molecular Biology (1.1k citations). Mais Hashem has collaborated with scholars based in Saudi Arabia, United States and Egypt. Frequent co-authors include Fowzan S. Alkuraya, Hanan E. Shamseldin, Mohammed A. Aldahmesh, Mohammed Al‐Owain, Niema Ibrahim, Eissa Faqeih, Ranad Shaheen, Tarfa Al‐Sheddi, Firdous Abdulwahab and Hanif Khalak. Their work appears in journals such as Human Genetics, The American Journal of Human Genetics, Genetics in Medicine, Clinical Genetics and Journal of Medical Genetics.

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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