Anju K. Philips - Concepedia

Author

Anju K. Philips

University of Helsinki ORCID

Also Known As

A.K. Philips, Anju K Philips, Anju K. Philips, Philips, Anju K., Philips, Anju Karingadampallil

Publications

356

Citations

H-Index

Concepts

All Affiliations

University of Helsinki University of the Arts Helsinki Radboud University Nijmegen Radboud University Medical Center Oulu University Hospital

About

Anju K. Philips is an author at University of Helsinki specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	106
2	Social Sciences	2	2	81
3	Arts	1	1	56
4	Natural Sciences	1	1	17
5	Public Health	1	1	19

Anju K. Philips

Publications

347

Citations

H-Index

Page 1

	Year	Citations
X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes Anju K. Philips, Auli Sirén, Kristiina Avela, Orphanet Journal of Rare Diseases	2014	81
The effect of listening to music on human transcriptome Chakravarthi Kanduri, Pirre Raijas, Minna Ahvenainen, PeerJ MusicAuditory ImageryNeuropsychologyCognitive ScienceMusical Aptitude	2015	56
The effect of music performance on the transcriptome of professional musicians Chakravarthi Kanduri, Tuire Kuusi, Minna Ahvenainen, Scientific Reports	2015	54
Music-listening regulates human microRNA expression Preethy Sasidharan Nair, Pirre Raijas, Minna Ahvenainen, Epigenetics	2020	50
Variants in<i>CUL4B</i>are Associated with Cerebral Malformations Anneke T. Vulto-van Silfhout, Tadashi Nakagawa, Nadia Bahi‐Buisson, Human Mutation Mendelian DisorderBrain DevelopmentNeurological DisorderGeneticsGenetic Disorder	2014	45
Music-performance regulates microRNAs in professional musicians Preethy Sasidharan Nair, Tuire Kuusi, Minna Ahvenainen, PeerJ MusicAuditory ImageryNeuropsychologyMusic CognitionGenetics	2019	25
Identification of <i>C12orf4</i> as a gene for autosomal recessive intellectual disability Anju K. Philips, Michele Pinelli, Charlotte I. de Bie, Clinical Genetics Dutch FamilyMendelian DisorderGenetic DisorderMedicineGenetics	2016	19
Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population D.L. Polla, Elisa Rahikkala, Michaela K. Bode, European Journal of Human Genetics BiologyPhylogeneticsNatural SciencesGeneticsEvolutionary Biology	2019	17

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