Shalini S. Nayak - Concepedia

Author

Shalini S. Nayak

Also Known As

Nayak, Shalini S., S Nayak, S S Nayak, SS Nayak, Shalini Nayak, Shalini S Nayak, Shalini S. Nayak, Shalini Sanjeeva Nayak, Subhashree Nayak, Yoxall CW

Publications

769

Citations

H-Index

Concepts

All Affiliations

Kasturba Medical College, Manipal Manipal Academy of Higher Education Inserm University Medical Center Hamburg-Eppendorf Sultan Qaboos University

About

Shalini S. Nayak is an author at Kasturba Medical College, Manipal specializing in medicine, pathology, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	381
2	Molecular Genetics	3	3	88
3	Cell Biology	2	2	209
4	Engineering	1	1	32
5	Biology	1	1	32

Shalini S. Nayak

Publications

597

Citations

H-Index

Page 1

	Year	Citations
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 Emmanuelle Szenker‐Ravi, Umut Altunoğlu, Marc Leushacke, Nature Signal TransductionMolecular PhysiologyDevelopmental BiologyBone Morphogenic ProteinSignaling Pathway	2018	190
Cornelia de Lange syndrome in diverse populations Leah Dowsett, Antonio R. Porras, Paul Kruszka, American Journal of Medical Genetics Part A Autoimmune DiseaseOphthalmologySclerodermaUpper Limb AnomaliesLange Syndrome	2019	53
The value of Bilicheck as a screening tool for neonatal jaundice in term and near‐term babies S Samanta, Mingpu Tan, Christopher M Kissack, Acta Paediatrica	2004	51
Clinical utility of fetal autopsy and its impact on genetic counseling Shalini S. Nayak, Anju Shukla, Leslie Lewis, Prenatal Diagnosis	2015	36
Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal Arthrogryposis Jessica X. Chong, Jared C. Talbot, Emily M. Teets, The American Journal of Human Genetics Novel Segmental AmyoplasiaDistal ArthrogryposisGeneticsPathologyMorphogenesis	2020	32
High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses Anna Hammarsjö, Maria Pettersson, David Chitayat, Journal of Human Genetics Skeletal CiliopathiesEngineeringParallel SequencingGeneticsPathology	2021	32
A retrospective cohort analysis of arthroscopic Bankart repair with or without remplissage in patients with off-track Hill-Sachs lesion evaluated for functional outcomes, recurrent instability, and range of motion Vivek Pandey, Lohith Gangadharaiah, Sandesh Madi, Journal of Shoulder and Elbow Surgery Recurrent InstabilitySurgical StabilizationRehabilitationSurgeryArthroscopic Technique	2019	31
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II) C.E. Flück, Johnny Deladoëy, Shalini S. Nayak, European Journal of Endocrinology	2001	30
Meckel syndrome: Clinical and mutation profile in six fetuses Periyasamy Radhakrishnan, Shalini S. Nayak, Anju Shukla, Clinical Genetics Exome SequencingGeneticsPathologyMolecular GeneticsDisease Gene Identification	2019	24
Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation Alban Ziegler, Rémi Duclaux‐Loras, Céline Revenu, The American Journal of Human Genetics	2021	23

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