# Joseph Glessner

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/joseph-glessner/

## Facts

| Field | Value |
| --- | --- |
| Citations | 30,617 |
| Field | Genomic variations and chromosomal abnormalities |
| h-index | 76 |
| i10-index | 178 |
| Last Known Institution | Children's Hospital of Philadelphia |
| OpenAlex ID | https://openalex.org/A5066789855 |
| ORCID iD | https://orcid.org/0000-0001-5131-2811 |
| Works | 297 |

## Researcher papers

Showing 12 of 14.

- [Functional impact of global rare copy number variation in autism spectrum disorders](https://scholariq.org/papers/functional-impact-of-global-rare-copy-number-variation-in-autism-spectrum/)
- [PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data](https://scholariq.org/papers/penncnv-an-integrated-hidden-markov-model-designed-for-high-resolution-copy/)
- [Autism genome-wide copy number variation reveals ubiquitin and neuronal genes](https://scholariq.org/papers/autism-genome-wide-copy-number-variation-reveals-ubiquitin-and-neuronal-genes/)
- [Common genetic variants on 5p14.1 associate with autism spectrum disorders](https://scholariq.org/papers/common-genetic-variants-on-5p14-1-associate-with-autism-spectrum-disorders/)
- [Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains](https://scholariq.org/papers/genome-wide-analyses-of-adhd-identify-27-risk-loci-refine-the-genetic/)
- [A genome-wide scan for common alleles affecting risk for autism](https://scholariq.org/papers/a-genome-wide-scan-for-common-alleles-affecting-risk-for-autism/)
- [Common variants at five new loci associated with early-onset inflammatory bowel disease](https://scholariq.org/papers/common-variants-at-five-new-loci-associated-with-early-onset-inflammatory-bowel/)
- [Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder](https://scholariq.org/papers/genome-wide-copy-number-variation-study-associates-metabotropic-glutamate/)
- [Individual common variants exert weak effects on the risk for autism spectrum disorders](https://scholariq.org/papers/individual-common-variants-exert-weak-effects-on-the-risk-for-autism-spectrum/)
- [A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci](https://scholariq.org/papers/a-genome-wide-meta-analysis-of-six-type-1-diabetes-cohorts-identifies-multiple/)
- [The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies](https://scholariq.org/papers/the-genomic-landscape-of-balanced-cytogenetic-abnormalities-associated-with/)
- [Integrative genomics identifies LMO1 as a neuroblastoma oncogene](https://scholariq.org/papers/integrative-genomics-identifies-lmo1-as-a-neuroblastoma-oncogene/)

## Researcher topics

- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)

## Researcher university

- [Children's Hospital of Philadelphia](https://scholariq.org/institutions/children-s-hospital-of-philadelphia/)

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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.