Mehmet Alikaşifoğlu

Author

Mehmet Alikaşifoğlu

Also Known As

Alikasifoglu Mehmet, Chris Scott, M Alikasifoglu, M Alikasifoğlu, M Alikaşifoğlu, M. ALIKASIFOGLU, M. Alikasifoglu, M. Alikasifoğlu, M. Alikaşifoglu, M. Alikaşifoğlu

172

Publications

Citations

H-Index

102

Concepts

All Affiliations

Hacettepe University

About

Mehmet Alikaşifoğlu is an author at Hacettepe University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	22	1.1K
2	Public Health	8	8	168
3	Social Sciences	2	2	84
4	Biostatistics	1	1	13
5	Immunology	1	1	25

Mehmet Alikaşifoğlu

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease Ender Karaca, Tamar Harel, Davut Pehli̇van, Neuron	2015	332
Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta Yasemin Alanay, Hrispima Avaygan, Natalia Camacho, The American Journal of Human Genetics SclerostinDevelopmental BiologyBone Morphogenic ProteinGeneticsOsteogenesis	2010	312
Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting: Expanding the Spectrum of Autosomal-Recessive ALX-Related Frontonasal Dysplasia Elif Uz, Yasemin Alanay, Dilek Aktaş, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyPathologyCraniofacial AnomaliesCraniofacial Development	2010	149
ALX4 dysfunction disrupts craniofacial and epidermal development Hülya Kayserili, Elif Uz, Carien M. Niessen, Human Molecular Genetics	2009	120
Paralog Studies Augment Gene Discovery: DDX and DHX Genes Ingrid S. Paine, Jennifer E. Posey, Christopher M. Grochowski, The American Journal of Human Genetics Functional GenomicsMedicineGeneticsGene CharacterizationPathway Analysis	2019	105
Violent behaviour among Turkish high school students and correlates of physical fighting Mehmet Alikaşifoğlu European Journal of Public Health	2004	94
Tumour necrosis factor α G→A −238 and G→A −308 polymorphisms in juvenile idiopathic arthritis Seza Özen, Mehmet Alikaşifoğlu, Ayşı̇n Bakkaloğlu, Lara D. Veeken	2002	81
Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate S. Lale Tokgözoğlu, Mehmet Alikaşifoğlu, İbrahim Ünsal, Heart	1999	78
Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey Nagehan Emiralioğlu, Ekim Z. Taşkıran, Can Koşukçu, Pediatric Pulmonology	2019	74
A Homozygous Deletion in <i>GRID2</i> Causes a Human Phenotype With Cerebellar Ataxia and Atrophy Gülen Eda Ütine, Göknur Haliloğlu, Bilge Volkan Salancı, Journal of Child Neurology Neurological DisorderGeneticsSynaptic SignalingSocial SciencesHomozygous Deletion	2013	72

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