Asmat Ullah - Concepedia

Author

Asmat Ullah

Also Known As

A. Ullah, A., Ullah, A.T. Ullah, Abeed Ullah, Asmat ULLAH, Asmat Ullah, Ayman T. Ullah, Ayman Teeham Ullah, Ayman Ullah, Dr. Asmat Ullah

143

Publications

980

Citations

H-Index

Concepts

All Affiliations

Quaid-i-Azam University Pakistan Institute of Medical Sciences Shaheed Zulfiqar Ali Bhutto Institute of Science and Technology Taibah University University of Copenhagen

About

Asmat Ullah is an author at Quaid-i-Azam University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	224
2	Engineering	2	2	117
3	Arts	1	1	19
4	Management	1	1	24
5	Public Health	1	1	13

Asmat Ullah

Publications

702

Citations

H-Index

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	Year	Citations
Numerical computation of buoyancy and radiation effects on MHD micropolar nanofluid flow over a stretching/shrinking sheet with heat source Saif Ur Rehman, Amna Mariam, Asmat Ullah, Case Studies in Thermal Engineering EngineeringFluid MechanicsMechanical EngineeringStretching/shrinking SheetHeat Source	2021	93
GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis–van Creveld syndrome Adrián Palencia‐Campos, Asmat Ullah, Julián Nevado, Human Molecular Genetics Developmental AnomalyGli1 InactivationDevelopmental BiologyMendelian DisorderGenetic Disorder	2017	53
FAM92A Underlies Nonsyndromic Postaxial Polydactyly in Humans and an Abnormal Limb and Digit Skeletal Phenotype in Mice Isabelle Schrauwen, Arnaud P. J. Giese, Abdul Aziz, Journal of Bone and Mineral Research	2018	42
Exome sequencing reveals a novel homozygous splice site variant in the WNT1 gene underlying osteogenesis imperfecta type 3 Muhammad Umair, Bader Alhaddad, Afzal Rafique, Pediatric Research SclerostinDevelopmental BiologyExome SequencingGeneticsOsteogenesis	2017	33
Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families. Asmat Ullah, Muhammad Umair, Maryam Yousaf, PubMed	2017	31
A novel deletion mutation in the<i>DSG4</i>gene underlies autosomal recessive hypotrichosis with variable phenotype in two unrelated consanguineous families Asmat Ullah, Syed Irfan Raza, Raja Hussain Ali, Clinical and Experimental Dermatology	2014	26
Novel homozygous sequence variants in the <i>GDF5</i> gene underlie acromesomelic dysplasia type‐grebe in consanguineous families Muhammad Umair, Afzal Rafique, Asmat Ullah, Congenital Anomalies Developmental BiologyShort Acromesomelic LimbsGdf5 GeneGenetic DisorderMendelian Disorder	2016	25
A Novel Heterozygous Intragenic Sequence Variant in DLX6 Probably Underlies First Case of Autosomal Dominant Split-Hand/Foot Malformation Type 1 Asmat Ullah, Anam Hammid, Muhammad Umair, Molecular Syndromology	2016	25
Customer Analysis Using Machine Learning-Based Classification Algorithms for Effective Segmentation Using Recency, Frequency, Monetary, and Time Asmat Ullah, Muhammad Ismail Mohmand, Hameed Hussain, Sensors Customer SatisfactionEngineeringBusiness IntelligenceCustomer ProfilingConsumer Research	2023	24
First direct evidence of involvement of a homozygous loss‐of‐function variant in the <i>EPS15L1</i> gene underlying split‐hand/split‐foot malformation Muhammad Umair, Asmat Ullah, Safdar Abbas, Clinical Genetics	2017	23

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