Orly Goldstein
发表
A. Boyko,
C. Bustamante,
J. Mezey,
2010,
Molecular vision.
V. Drory,
A. Orr-Urtreger,
M. Kedmi,
2022,
Neurology. Genetics.
G. Acland,
G. Aguirre,
A. Kukekova,
2010,
Genomics.
A. Boyko,
C. Bustamante,
J. Mezey,
2013,
Investigative ophthalmology & visual science.
Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia
G. Acland,
H. Huson,
A. Komáromy,
2013,
BMC Genetics.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2021,
Movement disorders : official journal of the Movement Disorder Society.
Yedael Y. Waldman,
A. Mirelman,
Nir Giladi,
2021,
Journal of genetics and genomics = Yi chuan xue bao.
B. Traynor,
V. Drory,
A. Orr-Urtreger,
2017,
Neurobiology of Aging.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2022,
Movement disorders : official journal of the Movement Disorder Society.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2019,
Molecular genetics and metabolism.
G. Acland,
G. Aguirre,
Á. Szél,
2011,
PloS one.
Inheritance, mode of inheritance, and candidate genes for primary hyperparathyroidism in Keeshonden.
K. Lindblad-Toh,
C. Wade,
R. Goldstein,
2007,
Journal of veterinary internal medicine.
N. Sabet,
S. McDonough,
R. Goldstein,
2009
.
Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3
G. Acland,
G. Aguirre,
A. Swaroop,
2009,
Mammalian Genome.
G. Acland,
G. Aguirre,
A. Swaroop,
2008
.
E. Kirkness,
E. Ostrander,
G. Acland,
2007,
Genome research.
Erez Y. Levanon,
Avi Shoshan,
Rotem Sorek,
2003,
Nature Biotechnology.
G. Aguirre,
T. Leeb,
M. Kondo,
2019,
Scientific Reports.
Orly Goldstein,
2014
.
G. Acland,
G. Aguirre,
Orly Goldstein,
2013,
Molecular vision.
G. Acland,
G. Aguirre,
Jennifer L. Johnson,
2010,
Mammalian Genome.
E. Kirkness,
E. Ostrander,
G. Acland,
2007
.
A. Mirelman,
Nir Giladi,
T. Gurevich,
2021,
Genes.
Nir Giladi,
Anat Mirelman,
Dvir Dahary,
2016,
Molecular genetics and metabolism.
B. Traynor,
V. Drory,
A. Renton,
2016,
Neurology.
V. Drory,
A. Orr-Urtreger,
M. Kedmi,
2019,
Journal of the Neurological Sciences.
G. Acland,
G. Aguirre,
S. Pearce-Kelling,
2006,
Genomics.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2020,
Movement disorders : official journal of the Movement Disorder Society.
A. Mirelman,
Nir Giladi,
G. Kavé,
2021,
Journal of Alzheimer's disease : JAD.
G. Acland,
G. Aguirre,
A. Philp,
2006,
Genomics.
A. Mirelman,
Nir Giladi,
T. Gurevich,
2023,
Molecular genetics and metabolism.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2021,
Journal of Parkinson's disease.
Yedael Y. Waldman,
A. Mirelman,
Nir Giladi,
2021,
Alzheimer's & dementia.
A. Mirelman,
Nir Giladi,
T. Shiner,
2021,
Molecular genetics and metabolism.
A. Mirelman,
Nir Giladi,
A. Orr-Urtreger,
2023,
Movement disorders clinical practice.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2020,
Scientific Reports.
A. Mirelman,
Nir Giladi,
T. Gurevich,
2023,
Parkinsonism & related disorders.
A. Mirelman,
I. Maidan,
Nir Giladi,
2022,
Clinical Neurophysiology.
A. Mirelman,
Nir Giladi,
G. Kavé,
2023,
BMC Neurology.
V. Drory,
A. Orr-Urtreger,
M. Kedmi,
2020,
Amyotrophic lateral sclerosis & frontotemporal degeneration.
Genomic deletion of CNGB3 is identical by descent in multiple canine breeds and causes achromatopsia
G. Acland,
H. Huson,
A. Komáromy,
2013,
BMC Genetics.
G. Acland,
G. Aguirre,
B. Zangerl,
2011,
Investigative ophthalmology & visual science.
A. Mirelman,
Nir Giladi,
J. Cedarbaum,
2021,
Journal of Neurology.
E. Kirkness,
E. Ostrander,
G. Acland,
2007,
Genome research.