Wesam Kurdi - Concepedia

Author

Wesam Kurdi

King Faisal Specialist Hospital & Research Centre ORCID

Also Known As

A Hellige, F Alresaini, H Al Sergani, K Malikov, Tinatin Tkemaladze, W Kurdi, W. Kurdi, W.I. Kurdi, Wesam I. Kurdi, Wesam I.Y. Kurdi

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre Alfaisal University King Saud University King Abdulaziz City for Science and Technology Security Forces Hospital

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	751
2	Public Health	3	3	75
3	Biochemistry	2	2	50
4	Social Sciences	1	1	30
5	Epidemiology	1	1	30

Wesam Kurdi

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin, Cell Reports	2014	465
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Human Genetics	2017	296
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
Expanding the genetic heterogeneity of intellectual disability Shams Anazi, Sateesh Maddirevula, Vincenzo Salpietro, Human Genetics Intellectual ImpairmentGeneticsDisabilityGenetic EpidemiologyGenetic Factor	2017	173
The genetic landscape of familial congenital hydrocephalus Ranad Shaheen, Mohammed Adeeb Sebai, Nisha Patel, Annals of Neurology	2017	144
The role of color Doppler imaging of the uterine arteries at 20 weeks' gestation in stratifying antenatal care Wesam Kurdi, S. Campbell, J. Aquilina, Ultrasound in Obstetrics and Gynecology	1998	124
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
Autozygome and high throughput confirmation of disease genes candidacy Sateesh Maddirevula, Fatema Alzahrani, Mohammed Al‐Owain, Genetics in Medicine	2018	112
Mutation in <i>MPDZ</i> causes severe congenital hydrocephalus Mohammed S. Al-Dosari, Mohammed Al‐Owain, Maha Tulbah, Journal of Medical Genetics	2012	100

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