Jehan Suleiman (J Suleiman)

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 12

Top Venues

American journal of medical genetics. Part A

Clinical genetics

European journal of pediatrics

Human molecular genetics

Al Tawam Hospital

University of Sydney (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Al Tawam Hospital

United Arab Emirates

Consultant Pediatric Neurologist :: Pediatric

Education History

University of Sydney

Australia

PHD :: Medicine

Publications

Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Correction to: Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review. European journal of pediatrics (2023)
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review. European journal of pediatrics (2023)
Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki
Correction to: Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review. European journal of pediatrics (2023)
Korbinian Maria Riedhammer, Anna L Burgemeister, Vincent Cantagrel, Jeanne Amiel, Karine Siquier-Pernet, Nathalie Boddaert, Jozef Hertecant, Patricia L Kannouche, Caroline Pouvelle, Stephanie Htun, Anne M Slavotinek, Christian Beetz, Dan Diego-Alvarez, Kapil Kampe, Nicole Fleischer, Zain Awamleh, Rosanna Weksberg, Matthias Elstner, Thomas Meitinger, Jehan Suleiman, Ayman W. El-Hattab
Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency. Human molecular genetics 31 (18) (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A 191 (3) (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A 191 (3) (2022)
Josephine Shuk Ching Chong, Ye Cao, Eva L W Fung, Soledad Kleppe, Karen W Gripp, Jozef Hertecant, Ayman W. El-Hattab, Jehan Suleiman, Gary Clark, Gretchen von Allmen, Olga Rodziyevska, Richard Alan Lewis, Jill Anne Rosenfeld, Jie Dong, null null, Xia Wang, Marcus J Miller, Weimin Bi, Pengfei Liu, Fernando Scaglia
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy. American journal of medical genetics. Part A 191 (3) (2022)
Christian Beetz, Najim Ameziane, Ameni Kdissa, Vasiliki Karageorgou, Peter Bauer, Jehan Suleiman, V Reid Sutton, Ayman W. El-Hattab
VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features. Clinical genetics 97 (4) (2019)
Jehan Suleiman, A M Al Hashem, B Tabarki, Khalid Al-Thihli, W Bi, Ayman W. El-Hattab
PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities. Clinical genetics 94 (3-4) (2018)
Jehan Suleiman, M Mundt, S Sampath, Ayman W. El-Hattab
TASP1 is deleted in an infant with developmental delay, microcephaly, distinctive facial features, and multiple congenital anomalies. Clinical genetics 94 (1) (2018)
Jehan Suleiman, D Allingham-Hawkins, M Hashem, H E Shamseldin, Fowzan Sami Alkuraya, Ayman W. El-Hattab
WDR45B-related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome. Clinical genetics 93 (2) (2017)

Jehan Suleiman.css-eqlu8i{font-size:small;padding-left:4px;} (J Suleiman)

Publication Activity (10 Years)

Top Topics

Top Venues

Jehan Suleiman (J Suleiman)