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Suliman Khan
Observed names:
Khan, Suliman,
S Khan,
S U Khan,
S. Khan
Institution:
Second Affiliated Hospital of Zhengzhou University
Observed institutions:
Jiangsu University,
Griffith University,
Quaid-i-Azam University,
Kohat University of Science and Technology,
Second Affiliated Hospital of Zhengzhou University,
Centogene (Germany)
show all 6
ORCID:
0000-0002-0745-7834
Observed ORCID:
0000-0002-0745-7834
OpenAlex ID:
A5086021989
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
2020
·
Lucia V. Schottlaender
, Rosella Abeti
, et al.
·
The American Journal of Human Genetics
·
88
PDF
Combining exome/genome sequencing with data repository analysis reveals novel gene–disease associations for a wide range of genetic disorders
2021
·
Aida M. Bertoli-Avella
, Krishna K. Kandaswamy
, et al.
·
Genetics in Medicine
·
61
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants
2020
·
Caroline Neuray
, Reza Maroofian
, et al.
·
Brain
·
54
PDF
A novel homozygous missense mutation in WNT10B in familial split‐hand/foot malformation
2011
·
S Khan
, S Basit
, et al.
·
Clinical Genetics
·
42
Prevalence of stroke above forty years.
2011
·
Q D Mohammad
, M Habib
, et al.
·
PubMed
·
41
Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis
2022
·
Ricardo Moreno Traspas
, Tze Shin Teoh
, et al.
·
Nature Genetics
·
27
PDF
PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy
2022
·
Hormos Salimi Dafsari
, Joshua G. Pemberton
, et al.
·
Annals of Clinical and Translational Neurology
·
25
PDF
Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal Agenesis
2020
·
Veronica Arora
, Suliman Khan
, et al.
·
Journal of the American Society of Nephrology
·
23
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders
2023
·
Rauan Kaiyrzhanov
, Aboulfazl Rad
, et al.
·
Brain
·
22
PDF
Biallelic ZNFX1 variants are associated with a spectrum of immuno‐hematological abnormalities
2021
·
Salem Alawbathani
, Ana Westenberger
, et al.
·
Clinical Genetics
·
20
PDF
A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family
2017
·
S. Khan
, M. Ansar
, et al.
·
British Journal of Dermatology
·
17
Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema
2023
·
Marius‐Ionuţ Iuraşcu
, Zsuzsanna Balla
, et al.
·
Clinical and Translational Allergy
·
16
Molecular study of X-linked ichthyosis: Report of a novel 2-bp insertion mutation in the STS and a very rare case of homozygous female patient
2014
·
Ghulam Murtaza
, Sumaira Siddiq
, et al.
·
Journal of Dermatological Science
·
16
ADAMTS19 ‐associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype
2020
·
Salam Massadeh
, Amal Alhashem
, et al.
·
Clinical Genetics
·
15
PDF
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation
2024
·
Marwan Nashabat
, Nasrinsadat Nabavizadeh
, et al.
·
Nature Communications
·
10
PDF
A disorder clinically resembling cystic fibrosis caused by biallelic variants in the AGR2 gene
2021
·
Aida Bertoli-Avella
, Ronja Hotakainen
, et al.
·
Journal of Medical Genetics
·
10
PDF
A door-to-door survey to estimate the prevalence of Parkinsonism in Pakistan
2016
·
Suliman Khan
, Ghulam Nabi
, et al.
·
Neuropsychiatric Disease and Treatment
·
10
PDF
Novel mutations in the genes TGM 1 and ALOXE 3 underlying autosomal recessive congenital ichthyosis
2015
·
Rahim Ullah
, Muhammad Ansar
, et al.
·
International Journal of Dermatology
·
9
De novo MCM6 variants in neurodevelopmental disorders: a recognizable phenotype related to zinc binding residues
2023
·
Daphne J. Smits
, Rachel Schot
, et al.
·
Human Genetics
·
8
PDF
Mapping of a novel locus for an autosomal recessive form of palmoplantar keratoderma on chromosome 3q27.2-q29
2010
·
S. Khan
, S. Muzaffar
, et al.
·
British Journal of Dermatology
·
6
Challenges Faced by PH.D. Scholars and Supervisors During COVID-19 in Turkey and Pakistan
2022
·
Sajjad Hussain
, Madiha Naz
, et al.
·
Pakistan Journal of Medical and Health Sciences
·
4
PDF
Adding evidence to the role of NEUROG1 in congenital cranial dysinnervation disorders
2021
·
Juliette Dupont
, José Pedro Vieira
, et al.
·
Clinical Genetics
·
4
PDF
Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism
2020
·
Steven R. Bentley
, Suliman Khan
, et al.
·
Frontiers in Neurology
·
4
PDF
UGT1A1 Gene Mutations in Pakistani Children Suffering from Inherited Nonhemolytic Unconjugated Hyperbilirubinemias
2013
·
Suliman Khan
, Muhammad Irfan
, et al.
·
Annals of Human Genetics
·
4
A novel biallelic nonsense variant in SLC38A3 causing epileptic encephalopathy in an Indian family
2022
·
Salem Alawbathani
, Suliman Khan
, et al.
·
Clinical Genetics
·
3
PDF
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Works count:
34
Citation count:
542
H-index:
14
I10-index:
17
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