# Marcella Rietschel

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/marcella-rietschel/

## Facts

| Field | Value |
| --- | --- |
| Citations | 90,580 |
| Field | Genetic Associations and Epidemiology |
| h-index | 133 |
| i10-index | 759 |
| Last Known Institution | Heidelberg University |
| OpenAlex ID | https://openalex.org/A5091088506 |
| ORCID iD | https://orcid.org/0000-0002-5236-6149 |
| Works | 1,550 |

## Researcher papers

- [Large recurrent microdeletions associated with schizophrenia](https://scholariq.org/papers/large-recurrent-microdeletions-associated-with-schizophrenia/)
- [Correlated gene expression supports synchronous activity in brain networks](https://scholariq.org/papers/correlated-gene-expression-supports-synchronous-activity-in-brain-networks/)
- [Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis](https://scholariq.org/papers/genome-wide-association-analyses-identify-new-risk-variants-and-the-genetic/)
- [A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis](https://scholariq.org/papers/a-genome-wide-association-study-confirms-pnpla3-and-identifies-tm6sf2-and-mboat7/)
- [Disruption of the neurexin 1 gene is associated with schizophrenia](https://scholariq.org/papers/disruption-of-the-neurexin-1-gene-is-associated-with-schizophrenia/)
- [Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo](https://scholariq.org/papers/genome-wide-association-for-major-depressive-disorder-a-possible-role-for-the/)
- [Copy number variations of chromosome 16p13.1 region associated with schizophrenia](https://scholariq.org/papers/copy-number-variations-of-chromosome-16p13-1-region-associated-with/)
- [Common variants on 8p12 and 1q24.2 confer risk of schizophrenia](https://scholariq.org/papers/common-variants-on-8p12-and-1q24-2-confer-risk-of-schizophrenia/)
- [Common variants at VRK2 and TCF4 conferring risk of schizophrenia](https://scholariq.org/papers/common-variants-at-vrk2-and-tcf4-conferring-risk-of-schizophrenia/)
- [Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples](https://scholariq.org/papers/genetic-association-of-the-human-corticotropin-releasing-hormone-receptor-1/)
- [Expanding the range of ZNF804A variants conferring risk of psychosis](https://scholariq.org/papers/expanding-the-range-of-znf804a-variants-conferring-risk-of-psychosis/)

## Researcher topics

- [Genetic Associations and Epidemiology](https://scholariq.org/topics/genetic-associations-and-epidemiology/)
- [Bipolar Disorder and Treatment](https://scholariq.org/topics/bipolar-disorder-and-treatment/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Neurotransmitter Receptor Influence on Behavior](https://scholariq.org/topics/neurotransmitter-receptor-influence-on-behavior/)
- [Schizophrenia research and treatment](https://scholariq.org/topics/schizophrenia-research-and-treatment/)

## Researcher university

- [Heidelberg University](https://scholariq.org/institutions/heidelberg-university/)

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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.