M. Verbitsky

发表

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Murim Choi, R. Lifton, M. Salvadori, 2014, Nature Genetics.

Mutations in DSTYK and dominant urinary tract malformations.

R. Ravazzolo, A. Latos-Bieleńska, V. D’Agati, 2013, The New England journal of medicine.

Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study

W. Chung, K. Marder, P. Appelbaum, 2019, Genetics in Medicine.

Gene expression signatures in chronic and aggressive periodontitis: a pilot study.

Paul Pavlidis, Miguel Verbitsky, Panos N Papapanou, 2004, European journal of oral sciences.

Olfaction in Parkin heterozygotes and compound heterozygotes

K. Marder, M. Rezak, L. Cote, 2010, Neurology.

Gene expression differences in mice divergently selected for methamphetamine sensitivity

T. Gilliam, A. Palmer, M. Verbitsky, 2005, Mammalian Genome.

Mixed nicotinic–muscarinic properties of the α9 nicotinic cholinergic receptor

M. Verbitsky, A. Elgoyhen, C. Rothlin, 2000, Neuropharmacology.

Mutations in the Parkinson's disease genes, Leucine Rich Repeat Kinase 2 (LRRK2) and Glucocerebrosidase (GBA), are not associated with essential tremor.

N. Park, Joseph H. Lee, E. Louis, 2010, Parkinsonism & related disorders.

The α9/α10-Containing Nicotinic ACh Receptor Is Directly Modulated by Opioid Peptides, Endomorphin-1, and Dynorphin B, Proposed Efferent Cotransmitters in the Inner Ear

J. Boulter, E. Glowatzki, M. Verbitsky, 2002, Molecular and Cellular Neuroscience.

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Craig S. Wong, H. Hakonarson, C. Willer, 2021, Journal of the American Society of Nephrology : JASN.

Altered hippocampal transcript profile accompanies an age-related spatial memory deficit in mice.

Paul Pavlidis, Miguel Verbitsky, Eric R Kandel, 2004, Learning & memory.

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.

Richard S. Lee, Amita Sharma, E. Mancini, 2015, American journal of human genetics.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Mixed nicotinic-muscarinic properties of the alpha9 nicotinic cholinergic receptor.

M. Verbitsky, A. Elgoyhen, C. Rothlin, 2000, Neuropharmacology.

Sonic Hedgehog Maintains Cellular and Neurochemical Homeostasis in the Adult Nigrostriatal Circuit

Luis E. Gonzalez-Reyes, J. Blesa, M. Verbitsky, 2012, Neuron.

High calcium permeability and calcium block of the α9 nicotinic acetylcholine receptor

S. Heinemann, M. Verbitsky, D. Vetter, 2000, Hearing Research.

Block of the α9 nicotinic receptor by ototoxic aminoglycosides

S. Heinemann, M. Verbitsky, D. Vetter, 2000, Neuropharmacology.

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Craig S. Wong, H. Hakonarson, A. Latos-Bieleńska, 2018, Nature Genetics.

Copy-number disorders are a common cause of congenital kidney malformations.

Stephan J Sanders, V. Jobanputra, W. Chung, 2012, American journal of human genetics.

Genomic imbalances in pediatric patients with chronic kidney disease.

A. Köttgen, A. Gharavi, K. Kiryluk, 2015, The Journal of clinical investigation.

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population

Karen Marder, Stanley Fahn, Andrew Browne, 2011, BMC Medical Genetics.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Craig S. Wong, E. Zackai, H. Hakonarson, 2017, The New England journal of medicine.

Genomic Disorders and Neurocognitive Impairment in Pediatric CKD.

Craig S. Wong, S. Hooper, A. Gharavi, 2017, Journal of the American Society of Nephrology : JASN.

ParseCNV2: a versatile and integrated tool for copy number variation association studies.

S. Sanna-Cherchi, M. Verbitsky, T. Lim, 2023, European journal of human genetics : EJHG.

Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.

K. Marder, M. Rezak, L. Cote, 2010, Archives of neurology.

Cognitive performance of GBA mutation carriers with early-onset PD

K. Marder, M. Rezak, L. Cote, 2012, Neurology.

The α9 Nicotinic Acetylcholine Receptor Shares Pharmacological Properties with Type A γ-Aminobutyric Acid, Glycine, and Type 3 Serotonin Receptors

M. Verbitsky, A. Elgoyhen, C. Rothlin, 1999 .

Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy

A. Christiano, S. Sanna-Cherchi, M. Verbitsky, 2020, Experimental dermatology.

Whole-Exome Sequencing in Adults With Chronic Kidney Disease

V. Jobanputra, V. D’Agati, C. Antignac, 2018, Annals of Internal Medicine.

Inducible Enhancement of Memory Storage and Synaptic Plasticity in Transgenic Mice Expressing an Inhibitor of ATF4 (CREB-2) and C/EBP Proteins

E. Kandel, T. Gilliam, D. Bartsch, 2003, Neuron.

Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.

K. Marder, M. Rezak, L. Cote, 2010, Archives of neurology.

Developmental expression profile of quaking, a candidate gene for schizophrenia, and its target genes in human prefrontal cortex and hippocampus shows regional specificity

Miguel Verbitsky, Lily Shiue, Manuel Ares, 2008, Journal of neuroscience research.

Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews

K. Marder, L. Cote, S. Fahn, 2013, Molecular genetics & genomic medicine.

Polyamine pathway contributes to the pathogenesis of Parkinson disease

G. Petsko, D. Ringe, K. Marder, 2010, Proceedings of the National Academy of Sciences.

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney

V. D’Agati, A. Gharavi, S. Sanna-Cherchi, 2015, Kidney international.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

hallucinations shows that peripheral ear symp- toms are always present. 22

M. Verbitsky, E. Prommer, P. Guth, 2005 .

Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors

M. Verbitsky, A. Elgoyhen, M. Lioudyno, 2000, Hearing Research.

Genomic Disorders in CKD across the Lifespan

Craig S. Wong, Joseph T. Glessner, J. Glessner, 2022 .

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease.

K. Marder, M. Rezak, L. Cote, 2009, Archives of neurology.

Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study

K. Marder, M. Rezak, L. Cote, 2010, Journal of the International Neuropsychological Society.

Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

K. Marder, M. Rezak, L. Cote, 2010, Journal of clinical and experimental neuropsychology.

Association of glucocerebrosidase mutations with dementia with lewy bodies.

K. Marder, R. Mayeux, L. Cote, 2009, Archives of neurology.

The alpha9 nicotinic acetylcholine receptor shares pharmacological properties with type A gamma-aminobutyric acid, glycine, and type 3 serotonin receptors.

M. Verbitsky, A. Elgoyhen, C. Rothlin, 1999, Molecular pharmacology.

Key roles of hydrophobic rings of TM2 in gating of the α9α10 nicotinic cholinergic receptor

C. Bouzat, M. Verbitsky, N. Weisstaub, 2005 .

Erratum : Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

D. Goldstein, S. Mane, G. Ardissino, 2017 .

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

A. Latos-Bieleńska, J. McKiernan, Shrikant Mane, 2023, Journal of the American Society of Nephrology : JASN.

Developmental expression profile of quaking, a candidate gene for schizophrenia, and its target genes in human prefrontal cortex and hippocampus shows regional specificity

M. Ares, V. Haroutunian, M. Verbitsky, 2008, Journal of neuroscience research.

Genomic imbalances in pediatric patients with chronic kidney disease.

Craig S. Wong, A. Köttgen, A. Gharavi, 2015, The Journal of clinical investigation.

Genomic Disorders in CKD across the Lifespan

Craig S. Wong, J. Glessner, H. Hakonarson, 2022, Journal of the American Society of Nephrology : JASN.

Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson disease.

K. Marder, M. Rezak, L. Cote, 2009, Archives of neurology.

Motor Phenotype of Lrrk2 G2019s Carriers in Early Onset Parkinson Disease Statistical Analyses Were Conducted Nih Public Access Author Manuscript

M. Verbitsky, R. Alcalay, H. Mejia‐Santana, 2022 .

Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.

K. Marder, M. Rezak, L. Cote, 2010, Archives of neurology.

Key roles of hydrophobic rings of TM2 in gating of the alpha9alpha10 nicotinic cholinergic receptor.

C. Bouzat, M. Verbitsky, N. Weisstaub, 2005, British journal of pharmacology.

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

N. Limdi, I. Kullo, Wei-Qi Wei, 2023, Nature Communications.

UNM Digital Repository UNM Digital Repository

H. Hakonarson, I. Ionita-Laza, A. Latos-Bieleńska, 2022 .

Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study

W. Chung, K. Marder, P. Appelbaum, 2019, Genetics in Medicine.

Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease

K. Marder, M. Rezak, L. Cote, 2010, Journal of clinical and experimental neuropsychology.