# Daniel G. Glaze

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/daniel-g-glaze/

## Facts

| Field | Value |
| --- | --- |
| Citations | 13,289 |
| Field | Genetics and Neurodevelopmental Disorders |
| h-index | 62 |
| i10-index | 142 |
| Last Known Institution | Baylor College of Medicine |
| OpenAlex ID | https://openalex.org/A5011312063 |
| ORCID iD | 0000-0001-6846-6446 |
| Works | 224 |

## Researcher papers

- [Rett syndrome: Revised diagnostic criteria and nomenclature](https://scholariq.org/papers/rett-syndrome-revised-diagnostic-criteria-and-nomenclature/)
- [Specific mutations in <i>Methyl-CpG-Binding Protein 2</i> confer different severity in Rett syndrome](https://scholariq.org/papers/specific-mutations-in-i-methyl-cpg-binding-protein-2-i-confer-different-severity/)
- [Characterization of Potocki-Lupski Syndrome (dup(17)(p11.2p11.2)) and Delineation of a Dosage-Sensitive Critical Interval That Can Convey an Autism Phenotype](https://scholariq.org/papers/characterization-of-potocki-lupski-syndrome-dup-17-p11-2p11-2-and-delineation-of/)
- [Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes](https://scholariq.org/papers/influence-of-mutation-type-and-x-chromosome-inactivation-on-rett-syndrome/)
- [Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)](https://scholariq.org/papers/multi-disciplinary-clinical-study-of-smith-magenis-syndrome-deletion-17p11-2/)
- [<i>Methyl-CpG-binding protein 2</i> (<i>MECP2</i>) mutation type is associated with disease severity in Rett syndrome](https://scholariq.org/papers/i-methyl-cpg-binding-protein-2-i-i-mecp2-i-mutation-type-is-associated-with/)
- [Autism and other neuropsychiatric symptoms are prevalent in individuals with <i>MeCP2</i> duplication syndrome](https://scholariq.org/papers/autism-and-other-neuropsychiatric-symptoms-are-prevalent-in-individuals-with-i/)
- [Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A](https://scholariq.org/papers/gene-dosage-is-a-mechanism-for-charcot-marie-tooth-disease-type-1a/)
- [Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males](https://scholariq.org/papers/increased-mecp2-gene-copy-number-as-the-result-of-genomic-duplication-in/)
- [Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities](https://scholariq.org/papers/loss-of-mecp2-in-aminergic-neurons-causes-cell-autonomous-defects-in/)
- [Assessing the Burden on Caregivers of MECP2 Duplication Syndrome](https://scholariq.org/papers/assessing-the-burden-on-caregivers-of-mecp2-duplication-syndrome/)

## Researcher topics

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Family and Disability Support Research](https://scholariq.org/topics/family-and-disability-support-research/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Child Nutrition and Feeding Issues](https://scholariq.org/topics/child-nutrition-and-feeding-issues/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)

## Researcher university

- [Baylor College of Medicine](https://scholariq.org/institutions/baylor-college-of-medicine/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.