Davor Lessel

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 5%percentile

0.350Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Combining genome-wide studies of breast, prostate, ovarian and endometrial cancers maps cross-cancer susceptibility loci and identifies new genetic associations

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.16.146803

Top 50%

0.350DataRank

Top 50%8 citations

Sara Lindström, Rayjean J. Hung, Kate Lawrenson, Marjanka K. Schmidt, Tracy A. O’Mara +95 more

Papers

Driven by 20 papers — median percentile 50. Top paper: “Identification of 22 susceptibility loci associated with testicular germ cell tumors”.

Identification of 22 susceptibility loci associated with testicular germ cell tumors

Nature Communications(2021)10.1038/s41467-021-24334-y

N/A

1.5DataRank · unranked

73 citations

Louise C. Pyle, Kevin T. Nead, Rona Wilf, Mingyao Li, Nandita Mitra +52 more

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00870-6

N/A

0.717DataRank · unranked

118 citations

Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo +95 more

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207

N/A

0.691DataRank · unranked

99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0.665DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 more

Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis

Diabetologia(2023)10.1007/s00125-023-05925-4

N/A

0.553DataRank · unranked

39 citations

Emmanouil Bouras, Andrei‐Emil Constantinescu, Kimberley Burrows, Caroline J. Bull, Emma E. Vincent +92 more

The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor

Cancers(2020)10.3390/cancers12113254

N/A

0.483DataRank · unranked

24 citations

Paula Paulo, Sofia Maia, Manuela Pinheiro, Ana Peixoto, Marta Cardoso +57 more

Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101097

N/A

0.460DataRank · unranked

10 citations

Young Nyun Park, Guy M. Lenk, Mariasavina Severino, Marcello Scala, Jonas Denecke +17 more

Association Study between Polymorphisms in DNA Methylation–Related Genes and Testicular Germ Cell Tumor Risk

Cancer Epidemiology Biomarkers & Prevention(2022)10.1158/1055-9965.epi-22-0123

N/A

0.373DataRank · unranked

11 citations

Maja Popović, Elena Isaevska, Fulvio Lazzarato, Valentina Fiano, Daniela Zugna +42 more

Combining genome-wide studies of breast, prostate, ovarian and endometrial cancers maps cross-cancer susceptibility loci and identifies new genetic associations

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.16.146803

Top 50%

0.350DataRank

Top 50%8 citations

Sara Lindström, Rayjean J. Hung, Kate Lawrenson, Marjanka K. Schmidt, Tracy A. O’Mara +95 more

Observational and genetic associations between cardiorespiratory fitness and cancer: a UK Biobank and international consortia study

British Journal of Cancer(2023)10.1038/s41416-023-02489-3

N/A

0.330DataRank · unranked

8 citations

Tomas I. Gonzales, Tessa Strain, Pedro F. Saint‐Maurice, D. Timothy Bishop, Stephen J. Chanock +89 more

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.012

N/A

0.292DataRank · unranked

6 citations

Anja Barešić, Iván K. Chinn, Jonathan May, Anu Goenka, Kate Chandler +91 more

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 more

Single substitution in H3.3G34 alters DNMT3A recruitment to cause progressive neurodegeneration

Cell(2023)10.1016/j.cell.2023.02.023

N/A

0DataRank · unranked

68 citations

Carol Chen, Augusto Faria Andrade, Nisha Kabir, Pariya Azarafshar, Shahir M. Morcos +40 more

Germline variation at 8q24 and prostate cancer risk in men of European ancestry

UNC Libraries(2023)10.17615/ejg2-ya10

N/A

0DataRank · unranked

0 citations

Victoria L. Stevens, Kan Wang, Nawaid Usmani, Radka Kaneva, C.A. Haiman +73 more

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

Nature Communications(2020)10.1038/s41467-020-18146-9

N/A

0DataRank · unranked

64 citations

Karim Harhouri, Morgane Le Mao, Geneviève Baujat, Sheela Nampoothiri, Hülya Kayserili +25 more

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00900-3

N/A

0DataRank · unranked

31 citations

Nghi Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff +60 more

DNA-binding affinity and specificity determine the phenotypic diversity in BCL11B-related disorders

UNC Libraries(2025)10.17615/dy6f-xt03

N/A

0DataRank · unranked

0 citations

Benjamin Cogné, Rachel Rabin, E Kessler, Céline Chappé, Melanie Brügger +92 more

Biallelic CACNA2D1 loss-of-function variants cause early-onset developmental epileptic encephalopathy

Brain(2022)10.1093/brain/awac081

N/A

0DataRank · unranked

41 citations

Leonie von Elsner, Tess Holling, Lauren Mattas, Jess Pickard, Davor Lessel +10 more

Genotype–phenotype correlations and novel molecular insights into the DHX30 -associated neurodevelopmental disorders

medRxiv(2020)10.1101/2020.09.24.20196097

N/A

0DataRank · unranked

0 citations

Nghi Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff +60 more

Werner syndrome in a Lebanese family

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62654

N/A

0DataRank · unranked

4 citations

Mona Nasrallah, Bianca Sievers, Junko Oshima, Davor Lessel, Batoul Jaafar

Davor Lessel

Indexed papers

Top data-sharing exemplar

Papers