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Hammer, Monia
38
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Online (38)
Mediatypes
Articles (Online) (15)
OpenAccess-fulltext (23)
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1
TRLS-13. MULTI-OMICS AND FUNCTIONAL PRECISION MEDICINE FOR ..:
Crawford, John R
;
Lo, Yan Yuen
;
Pagadala, Meghana S
...
Neuro-Oncology. 26 (2024) Supplement_4 - p. 0-0 , 2024
Link:
https://doi.org/10.1093/..
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2
P610: Identification of trinucleotide repeat expansions in ..:
Guidugli, Lucia
;
Hammer, Monia
;
Cao, Bryant
...
Genetics in Medicine Open. 2 (2024) - p. 101516 , 2024
Link:
https://doi.org/10.1016/..
?
3
Novel association of Dandy–Walker malformation with CAPN15 ..:
Beaman, M. Makenzie
;
Guidugli, Lucia
;
Hammer, Monia
...
American Journal of Medical Genetics Part A. 191 (2023) 11 - p. 2757-2767 , 2023
Link:
https://doi.org/10.1002/..
?
4
Insights into the perinatal phenotype of Kabuki syndrome in..:
Wigby, Kristen
;
Hammer, Monia
;
Tokita, Mari
...
American Journal of Medical Genetics Part A. 191 (2023) 4 - p. 930-940 , 2023
Link:
https://doi.org/10.1002/..
?
5
eP081: Dandy Walker malformation in three unrelated familie..:
Beaman, M. Makenzie
;
Guidugli, Lucia
;
Hammer, Monia
...
Genetics in Medicine. 24 (2022) 3 - p. S53-S54 , 2022
Link:
https://doi.org/10.1016/..
?
6
SORL1 mutation in a Greek family with Parkinson's disease a..:
Xiromerisiou, Georgia
;
Bourinaris, Thomas
;
Houlden, Henry
...
Annals of Clinical and Translational Neurology. 8 (2021) 10 - p. 1961-1969 , 2021
Link:
https://doi.org/10.1002/..
?
7
Exploring dementia and neuronal ceroid lipofuscinosis genes..:
Sassi, Celeste
;
Capozzo, Rosa
;
Hammer, Monia
...
Scientific Reports. 11 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
8
Shared Genetics of Multiple System Atrophy and Inflammatory..:
Shadrin, Alexey A.
;
Mucha, Sören
;
Ellinghaus, David
...
Movement Disorders. 36 (2020) 2 - p. 449-459 , 2020
Link:
https://doi.org/10.1002/..
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9
Blepharospasm: A genetic screening study in 132 patients:
Hammer, Monia
;
Abravanel, Alexandra
;
Peckham, Elizabeth
...
Parkinsonism & Related Disorders. 64 (2019) - p. 315-318 , 2019
Link:
https://doi.org/10.1016/..
?
10
Mendelian adult-onset leukodystrophy genes in Alzheimer's d..:
Sassi, Celeste
;
Nalls, Michael A.
;
Ridge, Perry G.
...
Neurobiology of Aging. 66 (2018) - p. 179.e17-179.e29 , 2018
Link:
https://doi.org/10.1016/..
?
11
Defects in the CAPN1 Gene Result in Alterations in Cerebell..:
Wang, Yubin
;
Hersheson, Joshua
;
Lopez, Dulce
...
Cell Reports. 16 (2016) 1 - p. 79-91 , 2016
Link:
https://doi.org/10.1016/..
?
12
The landscape of reported VUS in multi-gene panel and genom..:
Rehm, Heidi L.
;
Alaimo, Joseph T.
;
Aradhya, Swaroop
...
Genetics in Medicine. 25 (2023) 12 - p. 100947 , 2023
Link:
https://doi.org/10.1016/..
?
13
Clinical and genetic analyses of familial and sporadic fron..:
Capozzo, Rosa
;
Sassi, Celeste
;
Hammer, Monia B.
...
Alzheimer's & Dementia. 13 (2017) 8 - p. 858-869 , 2017
Link:
https://doi.org/10.1016/..
?
14
Clinical features and molecular genetics of two Tunisian fa..:
Hammer, Monia Benhamed
;
El Euch-Fayache, Ghada
;
Nehdi, Houda
...
Journal of Clinical Neuroscience. 21 (2014) 2 - p. 311-315 , 2014
Link:
https://doi.org/10.1016/..
?
15
Exploring dementia and neuronal ceroid lipofuscinosis genes..:
Sassi, Celeste
;
Capozzo, Rosa
;
Hammer, Monia
...
https://refubium.fu-berlin.de/handle/fub188/38142. , 2021
Link:
https://refubium.fu-berl..
1-15