Ranad Shaheen

8.3k citations

70 papers · 3.3k indexed · h-index 35

Impact in

Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
Biotechnology top 1%
- Microbial Inactivation Methods

Papers in

Genetics 32
- Genetic and Kidney Cyst Diseases 12
- Genomics and Rare Diseases 10
- Genetic Syndromes and Imprinting 8
- Genetics and Neurodevelopmental Disorders 7
Molecular Biology 50
- Bacillus and Francisella bacterial research 8
- RNA modifications and cancer 8
- Hedgehog Signaling Pathway Studies 8
- RNA regulation and disease 6

Co-authors: Fowzan S. Alkuraya Eissa Faqeih Maria A. Andersson Mirja Salkinoja‐Salonen David Jones Monika Ehling‐Schulz Ghada M. H. Abdel‐Salam Shinu Ansari
Journals: The American Journal of Human Genetics (13 papers)Journal of Medical Genetics (9 papers)Human Genetics (5 papers)Genetics in Medicine (4 papers)International Journal of Food Microbiology (3 papers)
Partner nations: Saudi Arabia United States Egypt

In The Last Decade

Ranad Shaheen

70 papers receiving 3.3k citations

Peers

Countries citing papers authored by Ranad Shaheen

Since Specialization

Citations

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

Fields of papers citing papers by Ranad Shaheen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ranad Shaheen, 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 Ranad Shaheen Line = papers co-authored together Ranad Shaheen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly Journal of Medical Genetics ·Ichrak Drissi, Emily V. Fletcher, Ranad Shaheen, Michael S. Nahorski, Amal Alhashem, Steven Lisgo, Alberto Fernández‐Jaén, Katherine Schon, K. Tlili-Graiess, Sarah Smithson, Susan Lindsay, Hayley J. Sharpe, Fowzan S. Alkuraya, Geoff Woods	2021	2
2	Complement C5a and Clinical Markers as Predictors of COVID-19 Disease Severity and Mortality in a Multi-Ethnic Population Frontiers in Immunology ·Farhan Cyprian, Muhammad Suleman, Ibrahim Abdelhafez, Asmma Doudin, Mohammed Danjuma, Fayaz Ahmad Mir, Aijaz Parray, Zohaib Yousaf, Mohammed Yaseen Ahmed Siddiqui, Alaaedin Abdelmajid, Mohammad Mulhim, Shaikha D. Al-Shokri, Mohammed Abukhattab, Ranad Shaheen, Eyad Elkord, Abdul Latif Al-Khal, Abdel‐Naser Elzouki, Guillermina Girardi	2021	14
3	Transcriptome of CD8+ tumor-infiltrating T cells: a link between diabetes and colorectal cancer Cancer Immunology Immunotherapy ·Reem Saleh, Varun Sasidharan Nair, Khaled Murshed, Mohamed Abu Nada, Eyad Elkord, Ranad Shaheen	2021	5
4	Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia American Journal of Medical Genetics Part A ·Ghada M. H. Abdel‐Salam, Inas Mazen, Maha M. Eid, Nour Ewida, Ranad Shaheen, Fowzan S. Alkuraya	2019	14
5	PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly Human Genetics ·Ranad Shaheen, Monika Tasak, Sateesh Maddirevula, Ghada M. H. Abdel‐Salam, Inas S. M. Sayed, Anas M. Alazami, Tarfa Al‐Sheddi, Eman Alobeid, Eric M. Phizicky, Fowzan S. Alkuraya	2019	68
6	Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans The American Journal of Human Genetics ·Ranad Shaheen, Nan Jiang, Fatema Alzahrani, Nour Ewida, Tarfa Al‐Sheddi, Eman Alobeid, Damir Musaev, Valentina Stanley, Mais Hashem, Niema Ibrahim, Firdous Abdulwahab, Abduljabbar Alshenqiti, Fatma Müjgan Sönmez, Nadia Saqati, Hamad Alzaidan, Mohammad M. Al‐Qattan, Futwan Al‐Mohanna, Joseph G. Gleeson, Fowzan S. Alkuraya	2019	21
7	Warsaw breakage syndrome: Further clinical and genetic delineation American Journal of Medical Genetics Part A ·Ebba Alkhunaizi, Ranad Shaheen, Sanjay Kumar Bharti, Ann M. Joseph‐George, Karen Chong, Ghada M. H. Abdel‐Salam, Mohammed Al‐Owain, Susan Blasér, Blake C. Papsin, Mohammed T. Butt, Mais Hashem, Nicole Martin, Ruth Godoy, Robert M. Brosh, Fowzan S. Alkuraya, David Chitayat	2018	16
8	Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden Genetics in Medicine ·Mohamed Abouelhoda, Turki M. Sobahy, Mohamed El-Kalioby, Nisha Patel, Hanan E. Shamseldin, Dorota Monies, Nada Al Tassan, Khushnooda Ramzan, Faiqa Imtiaz, Ranad Shaheen, Fowzan S. Alkuraya	2016	67
9	Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures Human Genetics ·Brahim Tabarki, Nabil Almajhad, Amal Alhashem, Ranad Shaheen, Fowzan S. Alkuraya	2016	51
10	Positional mapping of PRKD1 , NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus Journal of Medical Genetics ·Ranad Shaheen, Amal Al Hashem, Mohammed Hussien Alghamdi, Mohammed Zain Seidahmad, Salma M. Wakil, Khalid Dagriri, Bernard Keavney, Judith Goodship, Saad Alyousif, Fahad Alhabshan, Khalid Al-Hussein, Agaadir Almoisheer, Niema Ibrahim, Fowzan S. Alkuraya	2015	27
11	Revisiting disease genes based on whole-exome sequencing in consanguineous populations Human Genetics ·Ahmed Shamia, Ranad Shaheen, Nouran Sabbagh, Agaadir Almoisheer, Anason Halees, Fowzan S. Alkuraya	2015	7
12	The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population Genetics in Medicine ·Sarah M. Al-Qattan, Salma M. Wakil, Shamsa Anazi, Anas M. Alazami, Nisha Patel, Ranad Shaheen, Hanan E. Shamseldin, Samya Hagos, Haya M. AlDossari, Mustafa A. Salih, Heba Y. El Khashab, Amal Y. Kentab, Mohammed N. Al-Nasser, Fahad A. Bashiri, Namik Kaya, Mais Hashem, Fowzan S. Alkuraya	2014	11
13	Neu-Laxova Syndrome, an Inborn Error of Serine Metabolism, Is Caused by Mutations in PHGDH The American Journal of Human Genetics ·Ranad Shaheen, Zuhair Rahbeeni, Amal Alhashem, Eissa Faqeih, Qi Zhao, Yong Xiong, Agaadir Almoisheer, Sarah M. Al-Qattan, Halima A. Almadani, Noufa Alonazi, Badi Shoaib Albaqawi, Mohammad Saleh, Fowzan S. Alkuraya	2014	64
14	Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome The American Journal of Human Genetics ·Ranad Shaheen, Mona Aglan, Kim M. Keppler‐Noreuil, Eissa Faqeih, Shinu Ansari, Kim Horton, Adel M. Ashour, Maha S. Zaki, Fatema Alzahrani, Anna M. Cueto‐González, Ghada M. H. Abdel‐Salam, Samia A. Temtamy, Fowzan S. Alkuraya	2013	86
15	Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation Journal of Medical Genetics ·Ranad Shaheen, Anas M. Alazami, Muneera Alshammari, Eissa Faqeih, Nadia Alhashmi, Noon Mousa, Aisha Al-Sinani, Shinu Ansari, Fatema Alzahrani, Mohammed Al‐Owain, Zayed Al‐Zayed, Fowzan S. Alkuraya	2012	108
16	Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes European Journal of Human Genetics ·Ranad Shaheen, Eissa Faqeih, Muneera Alshammari, Abdulrahman Swaid, Lihadh Al‐Gazali, Elham Al Mardawi, Shinu Ansari, Sameera Sogaty, Mohammed Zain Seidahmed, Muhammed Al-Motairi, Chantal Farra, Wesam Kurdi, Shatha Alrasheed, Fowzan S. Alkuraya	2012	42
17	3M Syndrome: An Easily Recognizable yet Underdiagnosed Cause of Proportionate Short Stature The Journal of Pediatrics ·Mohammed S. Al‐Dosari, Muneera Alshammari, Ranad Shaheen, Eissa Faqeih, Mohammed A. Alghofely, Ahmad Amer Al Boukai, Fowzan S. Alkuraya	2012	26
18	Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly The American Journal of Human Genetics ·Fowzan S. Alkuraya, Xuyu Cai, Carina Emery, Ganeshwaran H. Mochida, Mohammed S. Al‐Dosari, Jillian M. Felie, R. Sean Hill, Brenda J. Barry, Jennifer N. Partlow, Generoso G. Gascon, Amal Y. Kentab, Mohammed M. Jan, Ranad Shaheen, Yuanyi Feng, Christopher A. Walsh	2011	2
19	Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs Clinical Genetics ·Ranad Shaheen, OY Al-Dirbashi, ZN Al‐Hassnan, Mohammed Al‐Owain, N Makhsheed, F Basheeri, MZ Seidahmed, Mustafa A. Salih, Eman Faqih, Hamad Zaidan, Moeen Al-Sayed, Zuhair Rahbeeni, Tarfa Al‐Sheddi, Mais Hashem, Wesam Kurdi, Nobuyuki Shimozawa, Fowzan S. Alkuraya	2010	14
20	Potential of selected infant food formulas for production of Bacillus cereus emetic toxin, cereulide International Journal of Food Microbiology ·Ranad Shaheen, Maria A. Andersson, Camelia Apetroaie, Anja Schulz, Monika Ehling‐Schulz, Velimatti Ollilainen, Mirja Salkinoja‐Salonen	2006	67

About Ranad Shaheen

Ranad Shaheen is a scholar working on Genetics, Molecular Biology, Biotechnology, Cell Biology and Developmental Biology, having authored 70 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (12 papers), Genomics and Rare Diseases (10 papers), Genetic Syndromes and Imprinting (8 papers), Bacillus and Francisella bacterial research (8 papers), RNA modifications and cancer (8 papers), Hedgehog Signaling Pathway Studies (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and RNA regulation and disease (6 papers). The work is most often cited by research in Genetics (1.2k citations), Biotechnology (365 citations), Molecular Biology (2.5k citations), Cell Biology (418 citations) and Clinical Biochemistry (100 citations). Ranad Shaheen has collaborated with scholars based in Saudi Arabia, United States and Egypt. Frequent co-authors include Fowzan S. Alkuraya, Eissa Faqeih, Maria A. Andersson, Mirja Salkinoja‐Salonen, David Jones, Monika Ehling‐Schulz, Ghada M. H. Abdel‐Salam, Shinu Ansari, Stefanie Keis and Hanan E. Shamseldin. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics, Human Genetics, Genetics in Medicine and International Journal of Food Microbiology.

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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