Henrike Heyne

Also affiliated with Institute for Molecular Medicine Finland, Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 16 papers. Top paper: “Rare coding variants in ten genes confer substantial risk for schizophrenia”.

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

Nature Communications(2020)10.1038/s41467-020-19966-5

N/A

4.9DataRank · unranked

176 citations

Elisabeth Widén, Sini Kerminen, Tuomo J Meretoja, Matti Pirinen, Pietro Della Briotta Parolo +94 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0.617DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery

Nature Medicine(2025)10.1038/s41591-025-03645-3

N/A

0.542DataRank · unranked

36 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

Nature Communications(2024)10.1038/s41467-024-50295-z

N/A

0.489DataRank · unranked

25 citations

Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie +4 more

Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.010

N/A

0.430DataRank · unranked

9 citations

Wenjun Jin, Christin Findeisen, Irene Valenzuela, Laura A. Devlin, Jill R. Murrell +35 more

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Nature Aging(2025)10.1038/s43587-025-00925-y

N/A

0.269DataRank · unranked

5 citations

Chenxi Qin, Moritz Krüger, Anna Kuukka, Aarno Palotie, Mark Daly +322 more

Limited overlap between genetic effects on disease susceptibility and disease survival

medRxiv(2023)10.1101/2023.10.10.23296544

N/A

0.269DataRank · unranked

5 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +19 more

Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events

medRxiv(2023)10.1101/2023.11.27.23297542

N/A

0.241DataRank · unranked

4 citations

Fanny‐Dhelia Pajuste, Julian Wanner, Jennifer I. Daniel Onwuchekwa, Reedik Mägi, Aarno Palotie +3 more

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

medRxiv(2024)10.1101/2024.09.11.24313458

N/A

0.104DataRank · unranked

1 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy

Molecular Psychiatry(2025)10.1038/s41380-025-03279-4

N/A

0DataRank · unranked

7 citations

Andrea Eoli, Ilona Krey, Bernt Popp, Vincent Strehlow, Dirk Alexander Wittekind +27 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406

N/A

0DataRank · unranked

1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more

Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.004

N/A

0DataRank · unranked

3 citations

Yin-Yuan Su, Siwei Chen, Akhil Velluva, Anna Kirstein, Antje Garten +9 more

Limited overlap between genetic effects on disease susceptibility and disease survival

Nature Genetics(2025)10.1038/s41588-025-02342-8

N/A

0DataRank · unranked

16 citations

Fanny‐Dhelia Pajuste, Kristina Zguro, Yipeng Cheng, Danielle E. Kurant, Andrea Eoli +20 more

A clustering approach to improve our understanding of the genetic and phenotypic complexity of chronic kidney disease

Scientific Reports(2024)10.1038/s41598-024-59747-4

N/A

0DataRank · unranked

5 citations

Susanne Ibing, Claudia Schurmann, Girish N. Nadkarni, Henrike Heyne, Erwin P. Böttinger +1 more