# James C. Mullikin

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/james-c-mullikin/

## Facts

| Field | Value |
| --- | --- |
| Citations | 102,634 |
| Field | Genomics and Phylogenetic Studies |
| h-index | 99 |
| i10-index | 206 |
| Last Known Institution | National Institutes of Health |
| OpenAlex ID | https://openalex.org/A5072393754 |
| ORCID iD | https://orcid.org/0000-0003-0825-3750 |
| Works | 298 |

## Researcher papers

- [The International HapMap Project](https://scholariq.org/papers/the-international-hapmap-project/)
- [A Draft Sequence of the Neandertal Genome](https://scholariq.org/papers/a-draft-sequence-of-the-neandertal-genome/)
- [Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2](https://scholariq.org/papers/early-onset-stroke-and-vasculopathy-associated-with-mutations-in-ada2/)
- [Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease](https://scholariq.org/papers/loss-of-function-mutations-in-tnfaip3-leading-to-a20-haploinsufficiency-cause-an/)
- [TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum](https://scholariq.org/papers/ttc21b-contributes-both-causal-and-modifying-alleles-across-the-ciliopathy/)
- [The DNA sequence and comparative analysis of human chromosome 20](https://scholariq.org/papers/the-dna-sequence-and-comparative-analysis-of-human-chromosome-20/)
- [Compound Heterozygosity for Loss-of-Function Lysyl-tRNA Synthetase Mutations in a Patient with Peripheral Neuropathy](https://scholariq.org/papers/compound-heterozygosity-for-loss-of-function-lysyl-trna-synthetase-mutations-in/)
- [Targeted resequencing implicates the familial Mediterranean fever gene <i>MEFV</i> and the toll-like receptor 4 gene <i>TLR4</i> in Behçet disease](https://scholariq.org/papers/targeted-resequencing-implicates-the-familial-mediterranean-fever-gene-i-mefv-i/)

## Researcher topics

- [Genomics and Phylogenetic Studies](https://scholariq.org/topics/genomics-and-phylogenetic-studies/)
- [Chromosomal and Genetic Variations](https://scholariq.org/topics/chromosomal-and-genetic-variations/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [RNA and protein synthesis mechanisms](https://scholariq.org/topics/rna-and-protein-synthesis-mechanisms/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

## Researcher university

- [National Institutes of Health](https://scholariq.org/institutions/national-institutes-of-health/)

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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.