# Center for Human Genetics

**Type:** Institutions  
**Canonical URL:** https://scholariq.org/institutions/center-for-human-genetics/

## Facts

| Field | Value |
| --- | --- |
| Avg h-index | 70.4 |
| Citations | 2,944,287 |
| City | Bar Harbor |
| Country | US |
| Description | Center for Human Genetics is a research organisation in Bar Harbor, US. OpenAlex records 9,242 works and 2,944,287 citations for it. 1,269 researchers list it as their most recent affiliation. |
| Homepage | http://www.centerforhumangenetics.org/ |
| OpenAlex ID | https://openalex.org/I4210105714 |
| Region | Maine |
| Researchers | 1,269 |
| ROR ID | https://ror.org/01gcrbc43 |
| Type | nonprofit |
| Works | 9,242 |

## University papers

- [Association between Microdeletion and Microduplication at 16p11.2 and Autism](https://scholariq.org/papers/association-between-microdeletion-and-microduplication-at-16p11-2-and-autism/)
- [Soft tissue and visceral sarcomas: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up☆](https://scholariq.org/papers/soft-tissue-and-visceral-sarcomas-esmo-euracan-genturis-clinical-practice/)
- [Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation](https://scholariq.org/papers/revised-diagnostic-criteria-for-neurofibromatosis-type-1-and-legius-syndrome-an/)
- [Nosology and classification of genetic skeletal disorders: 2019 revision](https://scholariq.org/papers/nosology-and-classification-of-genetic-skeletal-disorders-2019-revision/)
- [Gastrointestinal stromal tumours: ESMO–EURACAN–GENTURIS Clinical Practice Guidelines for diagnosis, treatment and follow-up](https://scholariq.org/papers/gastrointestinal-stromal-tumours-esmo-euracan-genturis-clinical-practice/)
- [Nosology and classification of genetic skeletal disorders: 2015 revision](https://scholariq.org/papers/nosology-and-classification-of-genetic-skeletal-disorders-2015-revision/)
- [A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)](https://scholariq.org/papers/a-homozygous-mutation-in-the-endothelin-3-gene-associated-with-a-combined/)
- [Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus](https://scholariq.org/papers/exonic-deletions-in-auts2-cause-a-syndromic-form-of-intellectual-disability-and/)
- [International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia](https://scholariq.org/papers/international-consensus-statement-on-the-diagnosis-multidisciplinary-management/)

## University top topics

Showing 8 of 25.

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)
- [Chromosomal and Genetic Variations](https://scholariq.org/topics/chromosomal-and-genetic-variations/)
- [Genomics and Chromatin Dynamics](https://scholariq.org/topics/genomics-and-chromatin-dynamics/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)

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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.