Timothy Cox
University of Missouri-Kansas City
H-index: 51
North America-United States
Top articles of Timothy Cox
Dysregulation in Spatiotemporal Expression of HMX1 Coordinated by Multifaceted Enhancers Drives an Auricular Disorder
bioRxiv
2024/4/2
Regulatory Functional Landscape of the HMX1 Gene for Normal Ear Development
2024/4/2
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development
Nature Communications
2024/1/2
Altering maternal calcium and phosphorus dietary intake induces persistent sex‐specific changes in the dentition of the offspring
Orthodontics & Craniofacial Research
2023/12/7
Recapitulation of POLR3-related hypomyelinating leukodystrophy phenotypes in mice using a PDGFRΑ-dependent POLR3B exon-loss genetic model
Journal of the Neurological Sciences
2023/12/1
Towards a clinical timeline of Alzheimer’s disease; a multivariate cognitive perspective
Alzheimer's & Dementia
2023/12
Timothy Cox
H-Index: 29
Hypomyelination, hypodontia and craniofacial abnormalities in a Polr3b mouse model of leukodystrophy
Brain
2023/12
How Can We Use Mathematical Modeling of Amyloid-β in Alzheimer’s Disease Research and Clinical Practices?
2023/11/24
Transcriptomic analysis reveals the role of SIX1 in mouse cranial neural crest patterning and bone development
Developmental Dynamics
2023/10
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature (vol 191A, 1227, 2023)
American Journal of Medical Genetics Part A
2023/5
The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4
Mammalian Genome
2023/9
Altering osteoclast numbers using CTSK models in utero affects mice offspring craniofacial morphology
Orthodontics & Craniofacial Research
2023/8
Triplication of the interferon receptor locus contributes to hallmarks of Down syndrome in a mouse model
Nature genetics
2023/6
Pdgfrα-dependent Polr3b Exon Loss Recapitulates POLR3-related Hypomyelinating Leukodystrophy Phenotypes in vivo (S2. 004)
2023/4/25
FOXI3 pathogenic variants cause one form of craniofacial microsomia
Nature Communications
2023/4/11
Muhammad Ansar
H-Index: 0
Periklis Makrythanasis
H-Index: 20
Bingqing Wang
H-Index: 3
Xiaopeng Xu
H-Index: 1
Qiang Li
H-Index: 25
Xavier Blanc
H-Index: 18
Hao Zhu
H-Index: 30
Qi Chen
H-Index: 9
Sunita Singh
H-Index: 12
Hongyuan Zhang
H-Index: 11
Xiaogang Wang
H-Index: 12
Peiwei Chen
H-Index: 1
Alessandro De Luca
H-Index: 38
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth
International Journal of Molecular Sciences
2023/2/21
Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans
Biology
2023/1/30
A Founder Intronic Variant in P3H1 Likely Results in Aberrant Splicing and Protein Truncation in Patients of Karen Descent with Osteogenesis Imperfecta Type VIII
Genes
2023/1/26
SERPINB3, Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis
Genes
2023/1/19
TRIM18 is a critical regulator of viral myocarditis and organ inflammation
Journal of biomedical science
2022/7/31
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