Elisa Molinari
Newcastle University
H-index: 13
Europe-United Kingdom
Top articles of Elisa Molinari
Spheroids, organoids and kidneys-on-chips: how complex human cellular models have assisted in the study of kidney disease and renal ciliopathies
2023/3
Elisa Molinari
H-Index: 7
Biallelic variants in CEP164 cause a motile ciliopathy‐like syndrome
Clinical Genetics
2023/3
Ben Green
H-Index: 13
James Thompson
H-Index: 61
Elisa Molinari
H-Index: 7
Gabrielle Wheway
H-Index: 16
Jane S Lucas
H-Index: 36
Update of genetic variants in CEP120 and CC2D2A—With an emphasis on genotype‐phenotype correlations, tissue specific transcripts and exploring mutation …
Molecular Genetics & Genomic Medicine
2021/12
Elisa Molinari
H-Index: 7
A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families
Human mutation
2021/10
Elisa Molinari
H-Index: 7
Shirlee Shril
H-Index: 21
Genetic compensation for cilia defects in cep290 mutants by upregulation of cilia-associated small GTPases
Journal of Cell Science
2021/7/15
Elisa Molinari
H-Index: 7
MO039IDENTIFICATION OF A RECURRENT SYNONYMOUS GENETIC VARIANT IN NPHP3 LEADING TO NEPHRONOPHTHISIS AND CONGENITAL HEPATIC …
Nephrology Dialysis Transplantation
2021/5/1
Elisa Molinari
H-Index: 7
Ian Wilson
H-Index: 22
Cell preservation methods and its application to studying rare disease
2021/4/1
Elisa Molinari
H-Index: 7
Gene and epigenetic editing in the treatment of primary ciliopathies
2021/1/1
Elisa Molinari
H-Index: 7
Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman
BMC nephrology
2020/12
Elisa Molinari
H-Index: 7
SO094HUMAN URINE-DERIVED RENAL EPITHELIAL CELLS PROVIDE INSIGHTS INTO THE PATHOGENICITY OF PKHD1 VARIANTS
Nephrology Dialysis Transplantation
2020/6/1
Elisa Molinari
H-Index: 7
Shalabh Srivastava
H-Index: 5
Disease modeling to understand the pathomechanisms of human genetic kidney disorders
2020/6/1
Elisa Molinari
H-Index: 7
Embryonic and foetal expression patterns of the ciliopathy gene CEP164
PLoS One
2020/1/28
Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome
Proceedings of the National Academy of Sciences
2020/1/14
Shirlee Shril
H-Index: 21
Elisa Molinari
H-Index: 7
Expression patterns of ciliopathy genes ARL3 and CEP120 reveal roles in multisystem development
BMC Developmental Biology
2020/12
Elisa Molinari
H-Index: 7
Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 alleles
BMC nephrology
2020/12
Elisa Molinari
H-Index: 7
Shalabh Srivastava
H-Index: 5
