# Elaine H. Zackai

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/elaine-h-zackai/

## Facts

| Field | Value |
| --- | --- |
| Citations | 50,221 |
| Field | Congenital heart defects research |
| h-index | 113 |
| i10-index | 545 |
| Last Known Institution | Children's Hospital of Philadelphia |
| OpenAlex ID | https://openalex.org/A5008262289 |
| ORCID iD | https://orcid.org/0000-0002-8002-893X |
| Works | 1,077 |

## Researcher papers

- [Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome](https://scholariq.org/papers/psychiatric-disorders-from-childhood-to-adulthood-in-22q11-2-deletion-syndrome/)
- [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/)
- [<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects](https://scholariq.org/papers/i-grin2b-i-encephalopathy-novel-findings-on-phenotype-variant-clustering/)
- [Human Chromosome 7: DNA Sequence and Biology](https://scholariq.org/papers/human-chromosome-7-dna-sequence-and-biology/)
- [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/)
- [Genetic Drivers of Kidney Defects in the DiGeorge Syndrome](https://scholariq.org/papers/genetic-drivers-of-kidney-defects-in-the-digeorge-syndrome/)
- [Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion](https://scholariq.org/papers/genetic-contributors-to-risk-of-schizophrenia-in-the-presence-of-a-22q11-2/)

## Researcher topics

- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Congenital Heart Disease Studies](https://scholariq.org/topics/congenital-heart-disease-studies/)
- [Craniofacial Disorders and Treatments](https://scholariq.org/topics/craniofacial-disorders-and-treatments/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## 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.
