Elif Yılmaz Güleç

Author

Elif Yılmaz Güleç

İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi ORCID

Also Known As

E., YilmazGulec, ELIF YILMAZ, ELİF YİLMAZ, Elif Gulec Yilmaz, Elif Gülec, Elif Y. Gulec, Elif YILMAZ GULEC, Elif YILMAZ GÜLEÇ, Elif Yilmaz, Elif Yilmaz Gulec

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi Sağlık Bilimleri Üniversitesi Texas Children's Hospital Baylor College of Medicine Radboud University Medical Center

About

Elif Yılmaz Güleç is an author at İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	792
2	Public Health	2	2	105
3	Engineering	1	1	33
4	Natural Sciences	1	1	138
5	Social Sciences	1	1	98

Elif Yılmaz Güleç

Publications

1.5K

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
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects Niki T. Loges, Dinu Antony, Aleš Maver, The American Journal of Human Genetics ChromatinGenome InstabilityDevelopmental BiologyChromatin StructureMendelian Disorder	2018	138
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance Davut Pehli̇van, Yavuz Bayram, Nilay Güneş, The American Journal of Human Genetics Candidate GenesDevelopmental BiologyOligogenic InheritanceGenetic DisorderComplex Trait	2019	118
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome Janson J. White, Juliana F. Mazzeu, Zeynep Coban‐Akdemir, The American Journal of Human Genetics Knockout MouseDevelopmental BiologyGenetic DisorderGeneticsGene Expression	2017	110
High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population Tadahiro Mitani, Sedat Işıkay, Alper Gezdirici, The American Journal of Human Genetics Neurodevelopmental DisordersNeurological DisorderGenetic DisorderPediatricsHigh Prevalence	2021	98
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility Asaf Ta‐Shma, Rim Hjeij, Zeev Perles, PLoS Genetics GeneticsMolecular GeneticsDisease Gene IdentificationReproductive BiologyEpigenetics	2018	87
Phenotypic expansion in <i> <scp>DDX</scp> 3X </i> – a common cause of intellectual disability in females Xia Wang, Jennifer E. Posey, Jill A. Rosenfeld, Annals of Clinical and Translational Neurology	2018	86
Megalencephalic leukoencephalopathy with subcortical cysts Eline M. Hamilton, Pınar Tektürk, Fia Cialdella, Neurology	2018	81
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype Marialetizia Motta, Giulia Fasano, Sina Gredy, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathogenesisGenetic Epidemiology	2021	77
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease Angad Jolly, Yavuz Bayram, Serap Turan, The Journal of Clinical Endocrinology & Metabolism	2019	75

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