Henrike Heyne

Hasso Plattner Institute — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

36h-index12.2kcitations119works8.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genomics and Rare Diseases(42), Genetics and Neurodevelopmental Disorders(27), Genetic Associations and Epidemiology(26), Genomic variations and chromosomal abnormalities(14), Epilepsy research and treatment(8)

Publications96 total

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
Molecular Psychiatry·2026Open Access
Leveraging a Genetic Proxy to Investigate the Effects of Lifelong Cardiac Sodium Channel Blockade
Circulation·2025Open Access
<i>USP25</i> in genetic generalized epilepsy: a gene under scrutiny
Brain·2025· 1 cited
GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy
Molecular Psychiatry·2025Open Access
Limited overlap between genetic effects on disease susceptibility and disease survival
Nature Genetics·2025· 4 citedOpen Access
Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity
The American Journal of Human Genetics·2025· 2 citedOpen Access
Leveraging a genetic proxy to investigate the effects of lifelong cardiac sodium channel blockade
2025Open Access
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery
Nature Medicine·2025· 21 citedOpen Access
Inherited infertility: Mapping loci associated with impaired female reproduction
The American Journal of Human Genetics·2024· 4 citedOpen Access
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks
2024· 1 citedOpen Access
Rare developmental disorder caused by variants in a small RNA gene
Nature·2024
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events
Nature Communications·2024· 17 citedOpen Access
Inherited infertility - mapping loci associated with impaired female reproduction
2024· 2 citedOpen Access
Decoding protein language models: insights from embedding space analysis
2024· 2 citedOpen Access
Evaluation of polygenic scoring methods in five biobanks shows larger variation between biobanks than methods and finds benefits of ensemble learning
The American Journal of Human Genetics·2024· 35 citedOpen Access
A unified framework for estimating country-specific cumulative incidence for 18 diseases stratified by polygenic risk
Nature Communications·2024· 23 citedOpen Access
A clustering approach to improve our understanding of the genetic and phenotypic complexity of chronic kidney disease
Scientific Reports·2024· 3 citedOpen Access
Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity
2024· 1 citedOpen Access
Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNA
Nature Communications·2024· 11 citedOpen Access
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events
2023· 4 citedOpen Access
page 1 of 5Next →

Frequent Co-authors

Dennis Lal(18), Patrick May(15), Sarah Weckhuysen(15), Johannes R. Lemke(14), Mark J. Daly(13), Ingo Helbig(12), Andrea Ganna(10), Aarno Palotie(10), Rikke S. Møller(10), Nina Mars(9), Hannah Stamberger(9), Hiltrud Muhle(9), Eduardo Pérez‐Palma(9), Reedik Mägi(8), Daniel P. Howrigan(8), Pasquale Striano(8), Tarjinder Singh(7), Peter De Jonghe(7), Renzo Guerrini(7), Steffen Syrbe(7)