Jehan Suleiman

1.1k citations

25 papers · 610 indexed · h-index 13

Co-authors: Russell C. Dale Ayman W. El‐Hattab Bethan Lang Fabienne Brilot Angela Vincent Mohammed Almannai Fernando Scaglia Deepak Gill
Topics: Genetics and Neurodevelopmental Disorders (10 papers)Genomics and Rare Diseases (7 papers)Autoimmune Neurological Disorders and Treatments (5 papers)
Cited by: Neurology Psychiatry and Mental health Infectious Diseases
Journals: Neurology The Journal of Infectious Diseases Epilepsia
Partner nations: United Arab Emirates United States Australia

In The Last Decade

Jehan Suleiman

24 papers receiving 600 citations

Peers

Countries citing papers authored by Jehan Suleiman

Since Specialization

Citations

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

Fields of papers citing papers by Jehan Suleiman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jehan Suleiman

This figure shows the co-authorship network connecting the top 25 collaborators of Jehan Suleiman. A scholar is included among the top collaborators of Jehan Suleiman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jehan Suleiman. Jehan Suleiman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review 2023 ·European Journal of Pediatrics ·(unknown),(unknown),Malak Alghamdi,Khalid Hundallah,Jehan Suleiman,Tawfeg Ben‐Omran,Majid Alfadhel,Mohammed Almannai,(unknown),Brahim Tabarki	0
2	Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy 2022 ·American Journal of Medical Genetics Part A ·(unknown),Ye Cao,Eva Fung,Soledad Kleppe,Karen W. Gripp,Jozef Hertecant,Ayman W. El‐Hattab,Jehan Suleiman,Gary Clark,Gretchen Von Allmen,(unknown),Richard A. Lewis,Jill A. Rosenfeld,Jie Dong,(unknown),Xia Wang,Marcus J. Miller,Weimin Bi,Pengfei Liu,Fernando Scaglia	2
3	Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency 2022 ·Frontiers in Pediatrics ·(unknown),Manju A. Kurian,Jehan Suleiman	1
4	Prevalence and patterns of anthropometric failure among under-five children in Nigeria: Evidence from the National nutrition and health survey, 2018. 2022 ·PubMed ·(unknown),Oyindamola B. Yusuf,Joshua Akinyemi,Folake Samuel,Imran Morhason‐Bello,Kabiru K. Salami,(unknown),(unknown),Adeyinka A. Aderinto,A R A Alada,Ayodele Samuel Jegede,Olufunmilayo I. Fawole,(unknown),(unknown),Jehan Suleiman,(unknown),(unknown),(unknown),(unknown),Isaac F. Adewole	3
5	VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features 2019 ·Clinical Genetics ·Christian Beetz,Najim Ameziane,(unknown),Vasiliki Karageorgou,Peter Bauer,Jehan Suleiman,V. Reid Sutton,Ayman W. El‐Hattab	4
6	Homozygous loss‐of‐function variants of TASP1 , a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies 2019 ·Human Mutation ·Jehan Suleiman,Korbinian M. Riedhammer,(unknown),(unknown),Laurie Werner,Mirjana Gušić,(unknown),Hessa S. Alsaif,(unknown),Nabil Moghrabi,(unknown),Moeenaldeen AlSayed,Weimin Bi,Srirangan Sampath,Fowzan S. Alkuraya,Ayman W. El‐Hattab	9
7	Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases 2018 ·Molecular Genetics and Metabolism ·Ayman W. El‐Hattab,Jehan Suleiman,Mohammed Almannai,Fernando Scaglia	116
8	ATP13A2 novel mutations causing a rare form of juvenile-onset Parkinson disease 2018 ·Brain and Development ·Jehan Suleiman,(unknown),Ayman W. El‐Hattab	12
9	Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus 2018 ·BMC Medical Genetics ·(unknown),Aisha Al‐Shamsi,Jehan Suleiman,Salma Ben‐Salem,Anne John,Ranjit Vijayan,Bassam R. Ali,Lihadh Al‐Gazali	10
10	PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities 2018 ·Clinical Genetics ·Jehan Suleiman,Amal Hashem,Brahim Tabarki,Khalid Al‐Thihli,Weimin Bi,Ayman W. El‐Hattab	8
11	Pediatric Multiple Sclerosis in the United Arab Emirates: Characteristics From a Multicenter Study and Global Comparison 2018 ·Journal of Child Neurology ·Fatima Ismail,Eliza Gordon‐Lipkin,(unknown),Iain Blair,Miklós Szólics,Taoufik Alsaadi,Faisal Aziz,Jehan Suleiman,Nicoline Schiess	13
12	WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome 2017 ·Clinical Genetics ·Jehan Suleiman,Diane Allingham‐Hawkins,Mais Hashem,Hanan E. Shamseldin,Fowzan S. Alkuraya,Ayman W. El‐Hattab	30
13	17q23.2q23.3 de novo duplication in association with speech and language disorder, learning difficulties, incoordination, motor skill impairment, and behavioral disturbances: a case report 2017 ·BMC Medical Genetics ·(unknown),Jehan Suleiman,(unknown),Shivendra Kishore,Arndt Rolfs,Ayman W. El‐Hattab	5
14	A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract 2016 ·Meta Gene ·Jozef Hertecant,(unknown),(unknown),Jehan Suleiman,Lihadh Al‐Gazali,Bassam R. Ali	19
15	Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family 2015 ·American Journal of Medical Genetics Part A ·(unknown),Anne John,Jehan Suleiman,Bassam R. Ali,Lihadh Al‐Gazali	13
16	The recognition and treatment of autoimmune epilepsy in children 2014 ·Developmental Medicine & Child Neurology ·Jehan Suleiman,Russell C. Dale	37
17	Autoantibodies to neuronal antigens in children with new‐onset seizures classified according to the revised ILAE organization of seizures and epilepsies 2013 ·Epilepsia ·Jehan Suleiman,Sukhvir Wright,Deepak Gill,Fabienne Brilot,Patrick Waters,(unknown),Peter Procopis,Anjan Nibber,Angela Vincent,Russell C. Dale,Bethan Lang	48
18	Immune-mediated steroid-responsive epileptic spasms and epileptic encephalopathy associated with VGKC-complex antibodies 2011 ·Developmental Medicine & Child Neurology ·Jehan Suleiman,Tanja Brenner,Deepak Gill,Christopher Troedson,(unknown),Fabienne Brilot,Angela Vincent,Bethan Lang,Russell C. Dale	32
19	SEVERE ENCEPHALOPATHY WITH SWINE ORIGIN INFLUENZA A H1N1 INFECTION IN CHILDHOOD: CASE REPORTS 2010 ·Neurology ·Richard Webster,Briony Hazelton,Jehan Suleiman,Kristine Macartney,Alison Kesson,Russell C. Dale	30
20	Isolation of Mycobacterium avium Complex from Bone Marrow Aspirates of AIDS Patients in Brazil 1993 ·The Journal of Infectious Diseases ·Joaquim Barreto,Moisés Palaci,Lucilaine Ferrazoli,Maria Conceição Martins,Jehan Suleiman,Rosemarie Lorenço,Orlando C. Ferreira,Lee W. Riley,William D. Johnson,(unknown)	37

About Jehan Suleiman

Jehan Suleiman is a scholar working on Genetics, Clinical Biochemistry and Neurology, having authored 25 papers that have together received 610 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (7 papers) and Autoimmune Neurological Disorders and Treatments (5 papers). The work is most often cited by research in Neurology (228 citations), Psychiatry and Mental health (96 citations) and Infectious Diseases (115 citations). Jehan Suleiman has collaborated with scholars based in United Arab Emirates, United States and Australia. Frequent co-authors include Russell C. Dale, Ayman W. El‐Hattab, Bethan Lang, Fabienne Brilot, Angela Vincent, Mohammed Almannai, Fernando Scaglia, Deepak Gill, Tanja Brenner and Bassam R. Ali. Their work appears in journals such as Neurology, The Journal of Infectious Diseases and Epilepsia.

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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