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de Nanclares, Guiomar Perez
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1

Multi-locus imprinting disturbance (MLID): interim joint st..:

Mackay, Deborah J. G. ; Gazdagh, Gabriella ; Monk, David...
Clinical Epigenetics.  16 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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2

Imprinting disorders:

Eggermann, Thomas ; Monk, David ; de Nanclares, Guiomar Perez...
Nature Reviews Disease Primers.  9 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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3

Recombinant growth hormone improves growth and adult height..:

Ertl, Diana-Alexandra ; de Nanclares, Guiomar Perez ; Jüppner, Harald...
European Journal of Endocrinology.  189 (2023)  1 - p. 123-131 , 2023
Link: https://doi.org/10.1093/..
 
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4

Novel genetic variants of KHDC3L and other members of the s..:

Pignata, Laura ; Cecere, Francesco ; Verma, Ankit...
Clinical Epigenetics.  14 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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5

First step towards a consensus strategy for multi-locus dia..:

Mackay, Deborah ; Bliek, Jet ; Kagami, Masayo...
Clinical Epigenetics.  14 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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6

Trans-acting genetic variants causing multilocus imprinting..:

Eggermann, Thomas ; Yapici, Elzem ; Bliek, Jet...
Clinical Epigenetics.  14 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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7

The role of ZFP57 and additional KRAB-zinc finger proteins ..:

Monteagudo-Sánchez, Ana ; Hernandez Mora, Jose Ramon ; Simon, Carlos...
Nucleic Acids Research.  48 (2020)  20 - p. 11394-11407 , 2020
Link: https://doi.org/10.1093/..
 
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8

Differences in expression rather than methylation at placen..:

Monteagudo-Sánchez, Ana ; Sánchez-Delgado, Marta ; Mora, Jose Ramon Hernandez...
Clinical Epigenetics.  11 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
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9

The most recurrent monogenic disorders that overlap with th..:

Vidal, S. ; Brandi, N. ; Pacheco, P....
European Journal of Paediatric Neurology.  23 (2019)  4 - p. 609-620 , 2019
Link: https://doi.org/10.1016/..
 
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10

Wind of change in pseudohypoparathyroidism and related diso..:

Lecumberri, Beatriz ; Martos-Moreno, Gabriel Ángel ; de Nanclares, Guiomar Perez
Endocrinología, Diabetes y Nutrición (English ed.).  65 (2018)  8 - p. 425-427 , 2018
Link: https://doi.org/10.1016/..
 
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11

Mutations causing acrodysostosis-2 facilitate activation of..:

Briet, Claire ; Pereda, Arrate ; Le Stunff, Catherine...
Human Molecular Genetics.  26 (2017)  20 - p. 3883-3894 , 2017
Link: https://doi.org/10.1093/..
 
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12

Erratum to: Imprinting disorders: a group of congenital dis..:

Eggermann, Thomas ; de Nanclares, Guiomar Perez ; Maher, Eamonn R....
Clinical Epigenetics.  8 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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13

Report of two novel mutations in PTHLH associated with brac..:

Thomas‐Teinturier, Cecile ; Pereda, Arrate ; Garin, Intza...
American Journal of Medical Genetics Part A.  170 (2015)  3 - p. 734-742 , 2015
Link: https://doi.org/10.1002/..
 
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14

Novel Microdeletions Affecting the GNAS Locus in Pseudohypo..:

Garin, Intza ; Elli, Francesca M. ; Linglart, Agnes...
The Journal of Clinical Endocrinology & Metabolism.  100 (2015)  4 - p. E681-E687 , 2015
Link: https://doi.org/10.1210/..
 
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15

Detection of Hypomethylation Syndrome among Patients with E..:

Perez-Nanclares, Gustavo ; Romanelli, Valeria ; Mayo, Sonia...
The Journal of Clinical Endocrinology & Metabolism.  97 (2012)  6 - p. E1060-E1067 , 2012
Link: https://doi.org/10.1210/..
 
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