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Steenackers, Ellen
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1

A Mosaic Variant in CTNNB1/β-catenin as a Novel Cause for O..:

Huybrechts, Yentl ; Appelman-Dijkstra, Natasha M ; Steenackers, Ellen...
The Journal of Clinical Endocrinology & Metabolism.  109 (2024)  7 - p. 1891-1898 , 2024
Link: https://doi.org/10.1210/..
 
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2

Genetic Screening of ZNF687 and PFN1 in a Paget's Disease o..:

Huybrechts, Yentl ; De Ridder, Raphaël ; Steenackers, Ellen...
Calcified Tissue International.  113 (2023)  5 - p. 552-557 , 2023
Link: https://doi.org/10.1007/..
 
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3

A recessive form of craniodiaphyseal dysplasia caused by a ..:

Hendrickx, Gretl ; Boudin, Eveline ; Steenackers, Ellen...
Bone.  167 (2023)  - p. 116633 , 2023
Link: https://doi.org/10.1016/..
 
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4

An Additional Lrp4 High Bone Mass Mutation Mitigates the So..:

Hendrickx, Gretl ; Boudin, Eveline ; Mateiu, Ligia...
Calcified Tissue International.  114 (2023)  2 - p. 171-181 , 2023
Link: https://doi.org/10.1007/..
 
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5

Camurati-Engelmann Disease Complicated by Hypopituitarism: ..:

Das, Liza ; Dhiman, Vandana ; Dutta, Pinaki...
AACE Clinical Case Reports.  8 (2022)  2 - p. 58-64 , 2022
Link: https://doi.org/10.1016/..
 
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6

Identification of Compound Heterozygous Variants in LRP4 De..:

Huybrechts, Yentl ; Boudin, Eveline ; Hendrickx, Gretl...
Genes.  13 (2021)  1 - p. 80 , 2021
Link: https://doi.org/10.3390/..
 
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7

Compound heterozygosity of mutations located in the first a..:

Huybrechts, Yentl ; Steenackers, Ellen ; Hamdy, Neveen...
Bone Reports.  13 (2020)  - p. 100604 , 2020
Link: https://doi.org/10.1016/..
 
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8

Spondylo-epi-metaphyseal dysplasia due to a homozygous miss..:

Das, Liza ; Dhiman, Vandana ; Van Hul, Wim...
Bone Reports.  12 (2020)  - p. 100245 , 2020
Link: https://doi.org/10.1016/..
 
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9

Conditional mouse models support the role of SLC39A14 (ZIP1..:

Hendrickx, Gretl ; Borra, Vere M. ; Steenackers, Ellen...
PLOS Genetics.  14 (2018)  4 - p. e1007321 , 2018
Link: https://doi.org/10.1371/..
 
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10

Genetic Screening of WNT4 and WNT5B in Two Populations with..:

Hendrickx, Gretl ; Boudin, Eveline ; Steenackers, Ellen...
Calcified Tissue International.  100 (2017)  3 - p. 244-249 , 2017
Link: https://doi.org/10.1007/..
 
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11

The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the ..:

Boudin, Eveline ; Yorgan, Timur ; Fijalkowski, Igor...
Journal of Bone and Mineral Research.  32 (2017)  8 - p. 1739-1749 , 2017
Link: https://doi.org/10.1002/..
 
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12

A Novel Domain-Specific Mutation in a Sclerosteosis Patient..:

Fijalkowski, Igor ; Geets, Ellen ; Steenackers, Ellen...
Journal of Bone and Mineral Research.  31 (2016)  4 - p. 874-881 , 2016
Link: https://doi.org/10.1002/..
 
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13

Mutations in sFRP1 or sFRP4 are not a common cause of crani..:

Boudin, Eveline ; Piters, Elke ; Fijalkowski, Igor...
Bone.  52 (2013)  1 - p. 292-295 , 2013
Link: https://doi.org/10.1016/..
 
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14

Novel SOST gene mutation in a sclerosteosis patient and her..:

Bhadada, Sanjay Kumar ; Rastogi, Ashu ; Steenackers, Ellen...
Bone.  52 (2013)  2 - p. 707-710 , 2013
Link: https://doi.org/10.1016/..
 
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15

A common LRP4 haplotype is associated with bone mineral den..:

Boudin, Eveline ; Steenackers, Ellen ; Freitas, Fenna de...
Bone.  53 (2013)  2 - p. 414-420 , 2013
Link: https://doi.org/10.1016/..
 
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