Overview
Laboratory of Neurogenetics and Development
Laboratory of Neurogenetics and Development\tThe research in my laboratory centers on discovery of gene mutations associated with brain malformations and investigation of how these genes direct the construction of brain. Three major projects encompass: 1) neural tube formation, 2) cell cycle regulation and its role in cellular patterning of brain, and 3) regulation of neuronal migration to establish brain architecture. These three areas of study, all NIH funded, are approached from both basic science and clinical genetic perspectives.\t
Neural tube closure -- This project examines mechanisms leading to neural tube defects (NTDs) and their prevention by folic acid and other agents. We previously modeled human NTD prevention by folic acid supplementation in the Crooked tail (Cd) mutant mouse line and showed Cd to be a remarkably good paradigm for investigation of the vitamin's effects on brain development. We identified the Cd gene mutation as defect in the Lrp6 co-receptor that is required for Wnt signaling, a key pathway in early development and tumor formation. The roles of Wnt pathway components in cellular and molecular events leading to NTDs and cortical dysplasia are studied. This work is being extended to a multi-center clinical effort to examine complex genetic traits associated with NTDs, using folate pathway and other candidate genes to screen clinical populations.\t
Neurogenesis -- Primary genesis and differentiation of neurons are examined in the context of cell cycle regulation and its relationship to brain structure. We have shown that the G1 active protein, cyclin D2, is expressed in developing mammalian brain in highly specific and restricted brain regions. Our studies of animals lacking cyclin D2 expression demonstrated that this isoform is necessary for the emergence and survival of cerebellar stellate interneurons, half of the granule cell population, and specific cerebral interneurons. Ongoing work addresses how molecular components of the cell cycle are controlled to generate specific neurons and whether this activating subunit of cyclin dependent kinases has a direct role in the differentiation of selected neuronal precursors. Recent investigations are using mouse and human embryonic stem cells to study the role of cyclins in the specification of neural progenitors.\t
Highlights
- 1Genetics in medicine : official journal of the American College of Medical Genetics · 2021
- 2Proceedings of the National Academy of Sciences of the United States of America · 2021
- 3Genetics in medicine open · 2024
Publications
Funding
Active
3 grants- Co-IR01NS138625-01A1Determining the role of Glucose transporter 1 in neural development and diseaseNational Institute of Neurological Disorders and Stroke · 2025–2030
- PIR01HD111089-04Understanding Genetic Complexity in Spina BifidaEunice Kennedy Shriver National Institute of Child Health and Human Development · 2023–2028
- Sub-PIU54NS117170-05 Project 1Epilepsy Multiplatform Variant Prediction (EpiMVP)National Institute of Neurological Disorders and Stroke · 2020–2026 · via University of Michigan
Completed grants (23)
- Co-IOT2OD037643-01Area of Interest 1: Community, Participant and Provider Engagement, Enrollment and Retention, Tasks 1, 2 and 3 - New York CoalitionOffice of the Director, NIH · 2024–2025 · via Icahn School of Medicine at Mount Sinai
- Co-IR01MH121922-014/4: Leveraging EHR-linked biobanks for deep phenotyping, polygenic risk score modeling, and outcomes analysis in psychiatric disordersNational Institute of Mental Health · 2019–2025
- Co-IOT2OD026556-01New York City Consortium for Precision Medicine (All of Us Research Program at WCM)Office of the Director, NIH · 2018–2024 · via Columbia University· 2 renewals
- PIR01NS105477-05Progenitor Regulation Underlying Cortical Interneuron SpecificationNational Institute of Neurological Disorders and Stroke · 2018–2024· 2 renewals
- Sub-PIR01NS102904-05Quantitative Imaging of Mouse Brain Development (CG)National Institute of Neurological Disorders and Stroke · 2019–2024 · via New York University School of Medicine (Grossman)
- KPBBRF 211269-01NARSAD Young Investigator GrantBrain & Behavior Research Foundation · 2021–2024
- KPF30HD100089-01A1The Role of Layer I Interneurons in the Activity-Dependent Assembly of the Somatosensory CortexEunice Kennedy Shriver National Institute of Child Health and Human Development · 2020–2023
- MPIF31NS122531-01Role of the U-12 dependent Minor Spliceosome in Early Embryo Development and Brain DiseaseNational Institute of Neurological Disorders and Stroke · 2021–2023Fellowship
- PITri-Sci 2019-022Molecular determinants of neural stem cell lineage progression and lifespan in mice and humansTri-Institutional Stem Cell Initiative (Weill Cornell) · 2020–2023
- PIP01HD067244-08S1Risk Genes and Environmental Interactions in Neural Tube DefectsEunice Kennedy Shriver National Institute of Child Health and Human Development · 2016–2022· 2 renewals
- Co-I567854Defective Lineage-dependent Precise Neocortical Circuit Assembly in ASD (PI: SHI)Simons Foundation Autism Research Initiative · 2019–2021
- KPF32NS108596-01The Role of Novel NMDA Receptor Variants in Human Brain Development and EpilepsyNational Institute of Neurological Disorders and Stroke · 2018–2019Fellowship
- PINREF 181836-01The Role of Novel NMDA Receptor Variants in Human Brain Development and EpilepsyNeurosurgery Research & Education Foundation · 2018–2019Fellowship
- PITSCI 2016-002Stem/Progenitor Origin of Neocortical Interneuron DiversityTri-Institutional Stem Cell Initiative (Weill Cornell) · 2016–2018
- Co-IUG3OD023183-01Columbia/Cornell/Harlem Hospital Precision Medicine Initiative HPOOffice of the Director, NIH · 2016–2018 · via Columbia University
- PIR01NS076465-05 EWEpigenome Interactions in Complex Neurogenetic DisordersNational Institute of Neurological Disorders and Stroke · 2011–2017
- PIR01NS058979-02Genetic Predisposition & Prevention of Neural Tube Defects (NTDs)NINDS · 2009–2011 · via NIH RePORTER
- MPIP30AR046121-06A1Project1: Role of the Wnt Co-receptor Lrp6 in regulation of Bone Density, GrowthNIAMS · 2006–2009 · via NIH RePORTER
- PIR01NS034998-09Crooked Tail: Gene Expression in a Neural Tube DefectNINDS · 1997–2007 · via NIH RePORTER
- PIR01NS035515-09ISOLATION & FUNCTION OF THE XLIS NEURONAL MIGRATION GENENINDS · 1996–2005 · via NIH RePORTER
Clinical research
Completed & closed trials (1)
- PIWCM-COVID19 BiobankWeill Medical College of Cornell University · CLOSED TO ACCRUAL (as of 2022)
News mentions
- $1.1 Million Grant Funds Research on Rare Neurodevelopmental DisorderJuly 23, 2025
The grant supports the launch of a natural history study for a rare neurodevelopmental disorder that causes developmental delays and seizures.
- Awards & Honors: DecemberDecember 30, 2024
Awards, honors and achievements for the month of December.
- New Atlas of mRNA Variants Captures Inner Workings of the BrainApril 9, 2024
Investigators at Weill Cornell Medicine have assembled the most comprehensive atlas to date of messenger RNA (mRNA) variants in the mouse and human brain, which will be important in understanding brain development, neuron specialization and other brain functions.
- Newly Discovered Bone Stem Cell Causes Premature Skull FusionSeptember 20, 2023
Craniosynostosis, the premature fusion of the top of the skull in infants, is caused by an abnormal excess of a previously unknown type of bone-forming stem cell, according to a preclinical study led by researchers at Weill Cornell Medicine.
- Awards and Honors Across Weill Cornell Medicine: November 30, 2021November 30, 2021
Awards, honors, prizes and achievements for the month of November.
Show 2 more mentions
- Study Recruiting 1,000 Healthcare Workers to Investigate Underlying Factors Driving COVID-19 OutcomesOctober 6, 2020
A study by investigators at Weill Cornell Medicine and NewYork-Presbyterian aims to answer one of COVID-19’s biggest mysteries: why do some people become severely ill, while others have no symptoms?
- Scientists Discover Genetic Cause of a Mysterious “Mosaic” DisorderNovember 22, 2019
The gene mutation that underlies a puzzling disorder featuring skin, brain and other abnormalities has been discovered by a team of scientists from Weill Cornell Medicine and the Fédération Hospitalo-Universitaire TRANSLAD (FHU-TRANSLAD) in France.
Mentoring
MD · 1
- YNYunan NieMD mentee · Class of 2019
PhD · 5
- AJAnoushka JoglekarTri-I Program in Computational Biology & Medicine (PhD) · Class of 2022
- TFTaylor FloydNeuroscience (PhD) · Class of 2022
- RBRaphael BendriemNeuroscience (PhD) · Class of 2019
- BMBerk MankaliyeNeuroscience (PhD)
Postdoc · 3
- SNSathiji NageshwaranPostdoc mentee · 2024–2025
- ASAnna SchluschePostdoc mentee · 2021–2021