Skip to main content
Enter the terms you wish to search for.
Select Search Option
This Site
All WCM Sites
Directory
Menu
Weill Cornell Medicine
Care
Discover
Teach
Feil Family Brain & Mind Research Institute
Explore this Website
Home
About BMRI
Toggle About BMRI menu options
Our Mission
Research Programs
Training
Facilities
Campus
Ways to Give
Administration
Faculty
Toggle Faculty menu options
Faculty, Primary Appointments
Faculty, Secondary Appointments
Affiliate Faculty
Research
Toggle Research menu options
Appel Institute
Center for Neurogenetics
Clinical & Translational Neuroscience Unit
Toggle Clinical & Translational Neuroscience Unit menu options
CTNU Director
CTNU Research Opportunities
Affiliate Institutions
New Grants
Publications
News
Toggle News menu options
Faculty Spotlight and Awards
New Grants
Events
Education
Toggle Education menu options
Neuroscience Graduate Program
Neuroscience Retreat
Leon Levy Fellowship
Research Residency
Brain Awareness
Medical School AOC
First Year Students
Core Facilities
Toggle Core Facilities menu options
Neuroanatomy EM Core
Neurogenetic Repository
BMRI Cores
Diversity and Inclusion
Toggle Diversity and Inclusion menu options
BMRI Diversity and Inclusion
Emerging Leaders in Neuroscience
BMRI Summer Scholars Program
Weill Cornell Medicine
Care
Discover
Teach
Home
About BMRI
Faculty
Research
News
Events
Education
Core Facilities
Diversity and Inclusion
Home
Publications
Publications
Appel Institute
Center for Neurogenetics
Clinical & Translational Neuroscience Unit
Affiliate Institutions
New Grants
Publications
Publications
Found 28 results
Author
Title
Type
[
Year
]
Filters:
Author
is
Ross, M Elizabeth
[Clear All Filters]
2014
Mirzaa G
,
Parry DA
,
Fry AE
,
Giamanco KA
,
Schwartzentruber J
,
Vanstone M
,
Logan CV
,
Roberts N
,
Johnson CA
,
Singh S
et al.
. 2014.
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
.
Nat Genet. 46(5):510-515.
2017
M Ross E
,
Mason CE
,
Finnell RH
. 2017.
Genomic approaches to the assessment of human spina bifida risk.
.
Birth Defects Res. 109(2):120-128.
Sudarov A
,
Zhang X-J
,
Braunstein L
,
LoCastro E
,
Singh S
,
Taniguchi Y
,
Raj A
,
Shi S-H
,
Moore H
,
M Ross E
. 2017.
Mature Hippocampal Neurons Require LIS1 for Synaptic Integrity: Implications for Cognition.
.
Biol Psychiatry.
Akimova D
,
Wlodarczyk BJ
,
Lin Y
,
M Ross E
,
Finnell RH
,
Chen Q
,
Gross SS
. 2017.
Metabolite profiling of whole murine embryos reveals metabolic perturbations associated with maternal valproate-induced neural tube closure defects.
.
Birth Defects Res. 109(2):106-119.
Elsaid MFawzi
,
Chalhoub N
,
Ben-Omran T
,
Kumar P
,
Kamel H
,
Ibrahim K
,
Mohamoud Y
,
Al-Dous E
,
Al-Azwani I
,
Malek JA
et al.
. 2017.
Mutation in noncoding RNA RNU12 causes early onset cerebellar ataxia.
.
Ann Neurol. 81(1):68-78.
Bendriem RM
,
M Ross E
. 2017.
Wiring the Human Brain: A User's Handbook.
.
Neuron. 95(3):482-485.
2018
Gupta I
,
Collier PG
,
Haase B
,
Mahfouz A
,
Joglekar A
,
Floyd T
,
Koopmans F
,
Barres B
,
Smit AB
,
Sloan SA
et al.
. 2018.
Single-cell isoform RNA sequencing characterizes isoforms in thousands of cerebellar cells.
.
Nat Biotechnol.
2019
Vabres P
,
Sorlin A
,
Kholmanskikh SS
,
Demeer B
,
St-Onge J
,
Duffourd Y
,
Kuentz P
,
Courcet J-B
,
Carmignac V
,
Garret P
et al.
. 2019.
Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.
.
Nat Genet.
Vabres P
,
Sorlin A
,
Kholmanskikh SS
,
Demeer B
,
St-Onge J
,
Duffourd Y
,
Kuentz P
,
Courcet J-B
,
Carmignac V
,
Garret P
et al.
. 2019.
Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.
.
Nat Genet.
Wolujewicz P
,
M Ross E
. 2019.
The search for genetic determinants of human neural tube defects.
.
Curr Opin Pediatr. 31(6):739-746.
Wolujewicz P
,
M Ross E
. 2019.
The search for genetic determinants of human neural tube defects.
.
Curr Opin Pediatr.
Bendriem RM
,
Singh S
,
Aleem AAbdel
,
Antonetti DA
,
M Ross E
. 2019.
Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex.
.
Elife. 8
2020
Vabres P
,
Sorlin A
,
Kholmanskikh SS
,
Demeer B
,
St-Onge J
,
Duffourd Y
,
Kuentz P
,
Courcet J-B
,
Carmignac V
,
Garret P
et al.
. 2020.
Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.
.
Nat Genet.
2021
Wolujewicz P
,
Aguiar-Pulido V
,
AbdelAleem A
,
Nair V
,
Thareja G
,
Suhre K
,
Shaw GM
,
Finnell RH
,
Elemento O
,
M Ross E
. 2021.
Genome-wide investigation identifies a rare copy-number variant burden associated with human spina bifida.
.
Genet Med.
Aguiar-Pulido V
,
Wolujewicz P
,
Martinez-Fundichely A
,
Elhaik E
,
Thareja G
,
Aleem AAbdel
,
Chalhoub N
,
Cuykendall T
,
Al-Zamer J
,
Lei Y
et al.
. 2021.
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk.
.
Proc Natl Acad Sci U S A. 118(51)
2022
Kholmanskikh S
,
Singh S
,
M Ross E
. 2022.
Activation of RhoC by regulatory ubiquitination is mediated by LNX1 and suppressed by LIS1.
.
Sci Rep. 12(1):16493.
Vo ML
,
Levy T
,
Lakhani S
,
Wang C
,
M Ross E
. 2022.
Adult-onset Niemann-Pick disease type C masquerading as spinocerebellar ataxia.
.
Mol Genet Genomic Med. :e1906.
Allen M
,
Huang BS
,
Notaras MJ
,
Lodhi A
,
Barrio-Alonso E
,
Lituma PJ
,
Wolujewicz P
,
Witztum J
,
Longo F
,
Chen M
et al.
. 2022.
Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca2+ signaling.
.
Mol Psychiatry.
Han X
,
Cao X
,
Aguiar-Pulido V
,
Yang W
,
Karki M
,
Ramirez PAndrea Pim
,
Cabrera RM
,
Lin YLinda
,
Wlodarczyk BJ
,
Shaw GM
et al.
. 2022.
CIC missense variants contribute to susceptibility for spina bifida.
.
Hum Mutat.
A Banday R
,
Stanifer ML
,
Florez-Vargas O
,
Onabajo OO
,
Papenberg BW
,
Zahoor MA
,
Mirabello L
,
Ring TJ
,
Lee C-H
,
Albert PS
et al.
. 2022.
Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries.
.
Nat Genet.
Hardwick SA
,
Hu W
,
Joglekar A
,
Fan L
,
Collier PG
,
Foord C
,
Balacco J
,
Lanjewar S
,
Sampson MMcGuirk
,
Koopmans F
et al.
. 2022.
Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue.
.
Nat Biotechnol.
Allen M
,
Huang BS
,
Notaras MJ
,
Lodhi A
,
Barrio-Alonso E
,
Lituma PJ
,
Wolujewicz P
,
Witztum J
,
Longo F
,
Chen M
et al.
. 2022.
Spontaneous generation of ASD astrocytes.
.
Mol Psychiatry. 27(5):2369.
2023
Bok S
,
Yallowitz AR
,
Sun J
,
McCormick J
,
Cung M
,
Hu L
,
Lalani S
,
Li Z
,
Sosa BR
,
Baumgartner T
et al.
. 2023.
A multi-stem cell basis for craniosynostosis and calvarial mineralization.
.
Nature. 621(7980):804-812.
Joglekar A
,
Hu W
,
Zhang B
,
Narykov O
,
Diekhans M
,
Balacco J
,
Ndhlovu LC
,
Milner TA
,
Fedrigo O
,
Jarvis ED
et al.
. 2023.
Single-cell long-read mRNA isoform regulation is pervasive across mammalian brain regions, cell types, and development.
.
bioRxiv.
2024
Buth JE
,
Dyevich CE
,
Rubin A
,
Wang C
,
Gao L
,
Marks T
,
Harrison MRm
,
Kong JH
,
M Ross E
,
Novitch BG
et al.
. 2024.
Foxp1 suppresses cortical angiogenesis and attenuates HIF-1alpha signaling to promote neural progenitor cell maintenance.
.
EMBO Rep.
1
(current)
2
next ›
last »