Nada Alsahan - Concepedia

Author

Nada Alsahan

King Faisal Specialist Hospital & Research Centre

Also Known As

.Nada alsahan, M Aldakheel, Musaad Abukhalid, N. Al-Sahan, Nada AlSahan, Nada Alsahan, Nada Al‐Sahan

Publications

885

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre King Abdulaziz City for Science and Technology Riyadh Armed Forces Hospital Security Forces Hospital Newcastle University

About

Nada Alsahan is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	378
2	Pathology	5	5	378
3	Molecular Genetics	1	1	41
4	Molecular Medicine	1	1	41
5	Nephrology	1	1	31

Nada Alsahan

Publications

717

Citations

H-Index

Page 1

	Year	Citations
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, The American Journal of Human Genetics SequencingNext-generation SequencingGeneticsPathologyOmics	2019	276
Molecular autopsy in maternal–fetal medicine Hanan E. Shamseldin, Wesam Kurdi, Fatima Almusafri, Genetics in Medicine	2017	123
Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families Hanan E. Shamseldin, Maha Tulbah, Wesam Kurdi, Genome Biology	2015	119
Identification of a novel MKS locus defined by<i>TMEM107</i>mutation Ranad Shaheen, Agaadir Almoisheer, Eissa Faqeih, Human Molecular Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMeckel-gruber Syndrome	2015	41
Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel Mohamed H. Al‐Hamed, Wesam Kurdi, Nada Alsahan, Journal of Medical Genetics	2016	33
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families Mohamed H. Al‐Hamed, Nada Alsahan, Sarah J. Rice, Pediatric Nephrology Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic Disease	2019	31
Lethal variants in humans: lessons learned from a large molecular autopsy cohort Hanan E. Shamseldin, Lama AlAbdi, Sateesh Maddirevula, Genome Medicine	2021	29
Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families Mohamed H. Al‐Hamed, John A. Sayer, Nada Alsahan, Journal of Nephrology	2020	19
<scp>M</scp>aternal floor infarction: <scp>M</scp>anagement of an underrecognized pathology Nada Alsahan, David Grynspan, Peter von Dadelszen, Journal of obstetrics and gynaecology research	2013	16
Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes Mohamed H. Al‐Hamed, Wesam Kurdi, Rubina Khan, Human Genetics Ciliopathy GenesDevelopmental AnomalyDevelopmental BiologyGenetic DisorderGenetics	2021	16

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