User profiles for K. A. Aldinger
Kimberly A. AldingerSeattle Children's Research Institute Verified email at seattlechildrens.org Cited by 5764 |
A human cell atlas of fetal gene expression
INTRODUCTION A reference atlas of human cell types is a major goal for the field. Here, we
set out to generate single-cell atlases of both gene expression (this study) and chromatin …
set out to generate single-cell atlases of both gene expression (this study) and chromatin …
Consensus paper: pathological role of the cerebellum in autism
SH Fatemi, KA Aldinger, P Ashwood, ML Bauman… - The Cerebellum, 2012 - Springer
… Aldinger and Millen. Immune involvement and its impact on autism symptom progression are
… Genetic Evidence for Cerebellar Involvement in Autistic Disorder (KA Aldinger and KJ Millen…
… Genetic Evidence for Cerebellar Involvement in Autistic Disorder (KA Aldinger and KJ Millen…
A human cell atlas of fetal chromatin accessibility
INTRODUCTION In recent years, the single-cell genomics field has made incredible
progress toward disentangling the cellular heterogeneity of human tissues. However, the …
progress toward disentangling the cellular heterogeneity of human tissues. However, the …
Anaplastic carcinoma of the thyroid. A review of 84 cases of spindle and giant cell carcinoma of the thyroid
KA Aldinger, NA Samaan, M Ibanez, CS Hill Jr - Cancer, 1978 - Wiley Online Library
Eighty‐four cases of spindle and giant cell carcinoma of the thyroid were reviewed. This is a
swiftly growing, and rapidly fatal neoplasm that generally develops in the elderly. Treatment …
swiftly growing, and rapidly fatal neoplasm that generally develops in the elderly. Treatment …
Population genetic study of the brain-derived neurotrophic factor (BDNF) gene
TL Petryshen, PC Sabeti, KA Aldinger, B Fry… - Molecular …, 2010 - nature.com
Genetic variants in the brain-derived neurotrophic factor (BDNF) gene, predominantly the
functional Val66Met polymorphism, have been associated with risk of bipolar disorder and …
functional Val66Met polymorphism, have been associated with risk of bipolar disorder and …
Spatial and cell type transcriptional landscape of human cerebellar development
KA Aldinger, Z Thomson, IG Phelps, P Haldipur… - Nature …, 2021 - nature.com
The human neonatal cerebellum is one-fourth of its adult size yet contains the blueprint
required to integrate environmental cues with developing motor, cognitive and emotional skills …
required to integrate environmental cues with developing motor, cognitive and emotional skills …
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation
KA Aldinger, OJ Lehmann, L Hudgins, VV Chizhikov… - Nature …, 2009 - nature.com
Dandy-Walker malformation (DWM), the most common human cerebellar malformation, has
only one characterized associated locus 1 , 2 . Here we characterize a second DWM-linked …
only one characterized associated locus 1 , 2 . Here we characterize a second DWM-linked …
Failure of human rhombic lip differentiation underlies medulloblastoma formation
Medulloblastoma (MB) comprises a group of heterogeneous paediatric embryonal
neoplasms of the hindbrain with strong links to early development of the hindbrain 1, 2, 3, 4. …
neoplasms of the hindbrain with strong links to early development of the hindbrain 1, 2, 3, 4. …
Unified rhombic lip origins of group 3 and group 4 medulloblastoma
Medulloblastoma, a malignant childhood cerebellar tumour, segregates molecularly into
biologically distinct subgroups, suggesting that a personalized approach to therapy would be …
biologically distinct subgroups, suggesting that a personalized approach to therapy would be …
Support for involvement of neuregulin 1 in schizophrenia pathophysiology
TL Petryshen, FA Middleton, A Kirby, KA Aldinger… - Molecular …, 2005 - nature.com
Schizophrenia is a common, multigenic psychiatric disorder. Linkage studies, including a
recent meta-analysis of genome scans, have repeatedly implicated chromosome 8p12-p23. 1 …
recent meta-analysis of genome scans, have repeatedly implicated chromosome 8p12-p23. 1 …