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Norah S. Alsaleh

ScholarGPS® ID: 71908306623809

Affiliation

Prince Sultan Military Medical City, Saudi Arabia

Affiliation History

Field

Medicine

Discipline

Pediatrics

Top Specialties

Medical Genetics

Metrics Summary

Publication Count

7

Predicted Citations

39

Predicted h-index

3

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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A Biallelic Variant in FRA10AC1 Is Associated With Neurodevelopmental Disorder and Growth Retardation (journal article) Alsaleh, Norah \| Alhashem, Amal \| Tabarki, Brahim \| Mohamed, Sarar \| Alharby, Essa \| Alkuraya, Fowzan S. \| Almontashiri, Naif A.M. Neurology Genetics, volume 8, issue 4 (2022). 10.1212/NXG.0000000000200010 Cited by (2) \| Cite \| Source
eP229: A case report of a complex chromosome 8 rearrangement with partial monosomy of 8p and partial trisomy of 8q (journal article) Salih, Rihab \| Ben Abdallah, Ines \| Shaikh, Shawana \| Rasheed, Sadia \| Alsaleh, Norah Genetics in Medicine, volume 24, issue 3, pages S142-S143 (2022). 10.1016/j.gim.2022.01.265 Cite \| Source
Expanding the KIF4A ‐associated phenotype (journal article) Kalantari, Silvia \| Carlston, Colleen \| Alsaleh, Norah \| Abdel‐Salam, Ghada M. H. \| Alkuraya, Fowzan \| Kato, Mitsuhiro \| Matsumoto, Naomichi \| Miyatake, Satoko \| Yamamoto, Tatsuya \| Fares‐Taie, Lucas \| ... \| Filges, Isabel American Journal of Medical Genetics Part A, volume 185, issue 12, pages 3728-3739 (2021). 10.1002/ajmg.a.62443 Cited by (5) \| Cite \| Source
Homozygous missense WIPI2 variants cause a congenital disorder of autophagy with neurodevelopmental impairments of variable clinical severity and disease course (journal article) Maroofian, Reza \| Gubas, Andrea \| Kaiyrzhanov, Rauan \| Scala, Marcello \| Hundallah, Khalid \| Severino, Mariasavina \| Abdel-Hamid, Mohamed S \| Rosenfeld, Jill A \| Ebrahimi-Fakhari, Darius \| Ali, Zahir \| ... \| Zaki, Maha S Brain Communications, volume 3, issue 3 (2021). 10.1093/braincomms/fcab183 Cited by (11) \| Cite \| Source
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome (journal article) AlKalaf, Heeba Y. \| AlHashem, Amal M. \| AlSaleh, Norah S. \| AlJohar, Norah M. \| Abo Thneen, Aliyah M. \| ElGhezal, Hatem M. \| Bouhjar, Inesse B. \| Tlili-Graiess, Kalthoum \| Sahari, Atif H. \| Tabarki, Brahim M. Neurosciences, volume 25, issue 4, pages 287-291 (2020). 10.17712/nsj.2020.4.20200045 Cited by (1) \| Cite \| Source
A novel truncating variant in ring finger protein 113A ( RNF113A ) confirms the association of this gene with X‐linked trichothiodystrophy (journal article) Mendelsohn, Bryce A. \| Beleford, Daniah T. \| Abu‐El‐Haija, Aya \| Alsaleh, Norah S. \| Rahbeeni, Zuhair \| Martin, Pierre‐Marie \| Rego, Shannon \| Huang, Alyssa \| Capodanno, Gina \| Shieh, Joseph T. \| ... \| Slavotinek, Anne M. American Journal of Medical Genetics Part A, volume 182, issue 3, pages 513-520 (2020). 10.1002/ajmg.a.61450 Cited by (12) \| Cite \| Source
Variable clinical course of identical twin neonates with Alström syndrome presenting coincidentally with dilated cardiomyopathy (journal article) Hollander, Seth A. \| Alsaleh, Norah \| Ruzhnikov, Maura \| Jensen, Kristen \| Rosenthal, David N. \| Stevenson, David A. \| Manning, Melanie American Journal of Medical Genetics Part A, volume 173, issue 6, pages 1687-1689 (2017). 10.1002/ajmg.a.38200 Cited by (5) \| Cite \| Source