Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

Inaam N. Mohammed · SciRah

Researcher profile · Semantic Scholar

Inaam N. Mohammed

Share profile

Inaam N. Mohammed — researcher profile on SciRah

h-index: 8
Works: 22
Citations: 238

Most-cited papers

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal‐Recessive Juvenile‐Onset Parkinson's Disease
Liena E. O. Elsayed, Valérie Drouet, T. Usenko, Inaam N. Mohammed +13 more
2016Annals of Neurology73 citations
Semantic Scholar
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +30 more
2016European Journal of Human Genetics31 citations Open access
Semantic Scholar
Research: Prevalence of neural tube defects Khartoum, Sudan August 2014–July 2015
I. Omer, Osman M. Abdullah, Inaam N. Mohammed, Lina A. Abbasher
2016BMC Research Notes28 citations Open access
Semantic Scholar
The quality of life among Sudanese children with epilepsy and their care givers.
Z. Abbas, M. Elseed, Inaam N. Mohammed
2014Sudanese Journal of Paediatrics18 citations
Semantic Scholar
The profile of childhood epilepsy in Sudan
Inaam N. Mohammed, M. Moneim, A. Rahman
201214 citations
Semantic Scholar
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +10 more
2018BMC Medical Genetics13 citations Open access
Semantic Scholar
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Ashraf Yahia, Liena E. O. Elsayed, Rémi Valter, Ahlam A. A. Hamed +25 more
2021Frontiers in Neurology10 citations Open access
Semantic Scholar
Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +10 more
2020Frontiers in Neurology8 citations Open access
Semantic Scholar
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing
Ashraf Yahia, I. Ben Ayed, Ahlam A. A. Hamed, Inaam N. Mohammed +20 more
2022Annals of Human Genetics7 citations
Semantic Scholar
Novel variants causing megalencephalic leukodystrophy in Sudanese families
M. Amin, Cédric Vignal, Ahlam A. A. Hamed, Inaam N. Mohammed +19 more
2021Journal of Human Genetics7 citations
Semantic Scholar
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
M. Amin, Cédric Vignal, Esraa Eltaraifee, Inaam N. Mohammed +12 more
2022BMC Medical Genomics6 citations Open access
Semantic Scholar
An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families
M. Koko, Ashraf Yahia, Liena E. O. Elsayed, Ahlam A. A. Hamed +17 more
2021Annals of Human Genetics6 citations
Semantic Scholar
Research: Prevalence of neural tube defects Khartoum, Sudan August 2014–July 2015
I. Omer, Osman M. Abdullah, Inaam N. Mohammed, Lina A. Abbasher
2016BMC Research Notes5 citations Open access
Semantic Scholar
Case Report: A New Family With Pontocerebellar Hypoplasia 10 From Sudan
M. Amin, Cédric Vignal, A. Hamed, Inaam N. Mohammed +19 more
2022Frontiers in Genetics3 citations Open access
Semantic Scholar
Congenital brain malformations in Sudanese children: an outpatient-based study.
Inaam N. Mohammed, S. Suliman, M. Elseed, A. Hamed +2 more
2018Sudanese Journal of Paediatrics3 citations Open access
Semantic Scholar
Paediatric neurology service in Sudan: Current situation and future challenges
M. Elseed, Inaam N. Mohammed, A. Hamed
20153 citations
Semantic Scholar
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
M. Koko, Maha A. Elseed, Inaam N. Mohammed, Ahlam A. A. Hamed +23 more
2024European Journal of Human Genetics2 citations Open access
Semantic Scholar
Epidemiology of epilepsy among school children in Khartoum State-2014.
A. Hamed, M. Elseed, Inaam N. Mohammed
20151 citations
Semantic Scholar
Exploring the molecular basis of hereditary spinocerebellar degeneration in a large Sudanese family
Arwa Babai, Liena E. O. Elsayed, Inaam N. Mohammed, Maha A. Elseed +4 more
2019Journal of Neurological Sciences0 citations
Semantic Scholar
Clinical profile of pediatric neurological disorders as seen in outpatient clinic in Khartoum, Sudan
Inaam N. Mohammed, M. Elseed, A. Hamed
20150 citations
Semantic Scholar
Successful medical treatment of a large thoracic hydatid cyst in a child
Inaam N. Mohammed, A. Arabi, A. Baraka, Z. Karrar
20120 citations
Semantic Scholar
Misdiagnosis of long QT syndrome
Sulafa K. M. Ali, Inaam N. Mohammed
20120 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Liena E. O. Elsayed×12
Invite
Liena E. O. Elsayed — researcher profile on SciRah
Maha A. Elseed×12
Invite
Maha A. Elseed — researcher profile on SciRah
Ahlam A. A. Hamed×11
Invite
Ahlam A. A. Hamed — researcher profile on SciRah
A. Ahmed×10
Invite
A. Ahmed — researcher profile on SciRah

×9

Invite

M. Koko — researcher profile on SciRah

Invite

Arwa Babai — researcher profile on SciRah

Ashraf Yahia×8

Invite

Ashraf Yahia — researcher profile on SciRah

Invite

G. Stevanin — researcher profile on SciRah

Invite

M. Ibrahim — researcher profile on SciRah

Invite

R. Abubaker — researcher profile on SciRah

M. I. Elbashir×5

Invite

M. I. Elbashir — researcher profile on SciRah

Invite

A. Brice — researcher profile on SciRah