Alice Costantini - Concepedia

Author

Alice Costantini

University of Helsinki ORCID

Also Known As

A Costantini, A. Costantini, Alice Costantini

Publications

645

Citations

H-Index

Concepts

All Affiliations

University of Helsinki Helsinki University Hospital Karolinska Institutet Karolinska University Hospital Folkhälsans Forskningscentrum

About

Alice Costantini is an author at University of Helsinki specializing in medicine, genetics, and osteoporosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	91
2	Pathology	4	4	77
3	Molecular Genetics	2	2	31
4	Orthopaedics	2	2	31
5	Rheumatology	1	1	17

Alice Costantini

Publications

417

Citations

H-Index

Page 1

	Year	Citations
PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants Anders Kämpe, Alice Costantini, Riikka E. Mäkitie, Osteoporosis International	2017	50
<i>PLS3</i> Deletions Lead to Severe Spinal Osteoporosis and Disturbed Bone Matrix Mineralization Anders Kämpe, Alice Costantini, Yael Levy‐Shraga, Journal of Bone and Mineral Research	2017	50
Spondyloocular Syndrome: Novel Mutations in <i>XYLT2</i> Gene and Expansion of the Phenotypic Spectrum Fulya Taylan, Alice Costantini, Nicole Coles, Journal of Bone and Mineral Research	2016	48
A novel <i>MYT1L</i> mutation in a patient with severe early‐onset obesity and intellectual disability Petra Loid, Riikka E. Mäkitie, Alice Costantini, American Journal of Medical Genetics Part A	2018	32
Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23 Riikka E. Mäkitie, Anders Kämpe, Alice Costantini, Journal of Bone and Mineral Research	2020	32
Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility Alice Costantini, Sini Skarp, Anders Kämpe, Frontiers in Endocrinology	2018	31
A novel frameshift deletion in PLS3 causing severe primary osteoporosis Alice Costantini, Panagiotis Krallis, Anders Kämpe, Journal of Human Genetics Bone DiseaseGeneticsNovel Frameshift DeletionPathologyMedicine	2018	26
Unique, Gender-Dependent Serum microRNA Profile in PLS3 Gene-Related Osteoporosis Riikka E. Mäkitie, Matthias Hackl, Moritz Weigl, Journal of Bone and Mineral Research	2020	22
Fetomaternal Adrenomedullin Levels in Diabetic Pregnancy Raffaele Iorio, Emanuela Marinoni, Gabrielle Urban, Hormone and Metabolic Research	2001	20
Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with “corner fractures” Alice Costantini, Helena Valta, Nissan Baratang, Bone GeneticsPathologySpondylometaphyseal DysplasiaMedicine“ Corner Fractures	2018	20

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