# Michael J. Bamshad

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/michael-j-bamshad/

## Facts

| Field | Value |
| --- | --- |
| Citations | 46,653 |
| Field | Genomics and Rare Diseases |
| h-index | 98 |
| i10-index | 331 |
| Last Known Institution | Seattle Children's Hospital |
| OpenAlex ID | https://openalex.org/A5064174809 |
| ORCID iD | https://orcid.org/0000-0002-9647-0861 |
| Works | 537 |

## Researcher papers

- [The Influence of <i>CCL3L1</i> Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility](https://scholariq.org/papers/the-influence-of-i-ccl3l1-i-gene-containing-segmental-duplications-on-hiv-1-aids/)
- [International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases](https://scholariq.org/papers/international-cooperation-to-enable-the-diagnosis-of-all-rare-genetic-diseases/)
- [Somatic Mutations in Cerebral Cortical Malformations](https://scholariq.org/papers/somatic-mutations-in-cerebral-cortical-malformations/)
- [Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages](https://scholariq.org/papers/deep-common-ancestry-of-indian-and-western-eurasian-mitochondrial-dna-lineages/)
- [Mutations in <i>RSPH1</i> Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype](https://scholariq.org/papers/mutations-in-i-rsph1-i-cause-primary-ciliary-dyskinesia-with-a-unique-clinical/)
- [Insights into genetics, human biology and disease gleaned from family based genomic studies](https://scholariq.org/papers/insights-into-genetics-human-biology-and-disease-gleaned-from-family-based/)
- [Spectrum of <i>MLL2</i> (<i>ALR</i>) mutations in 110 cases of Kabuki syndrome](https://scholariq.org/papers/spectrum-of-i-mll2-i-i-alr-i-mutations-in-110-cases-of-kabuki-syndrome/)
- [Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes](https://scholariq.org/papers/functional-dysregulation-of-cdc42-causes-diverse-developmental-phenotypes/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Researcher university

- [Seattle Children's Hospital](https://scholariq.org/institutions/seattle-children-s-hospital/)

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