Nicholas Katsanis

FORTH Institute of Molecular Biology and Biotechnology

Also affiliated with Institute of Molecular Biology and Biotechnology, Io Therapeutics (United States), Foundation for Research and Technology Hellas

Biochemistry, Genetics and Molecular Biology

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 1%percentile

4.7Author 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.

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Papers

Driven by 24 papers — median percentile 95. Top paper: “A cross-disorder dosage sensitivity map of the human genome”.

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

Nature Genetics(2020)10.1038/s41588-020-0707-1

N/A

2.0DataRank · unranked

35 citations

Onuralp Söylemez, Aysegül Ozanturk, Niki Mourtzi, Sebastian Akle, Irwin Jungreis +16 more

A cross-disorder dosage sensitivity map of the human genome

medRxiv(2021)10.1101/2021.01.26.21250098

N/A

2.0DataRank · unranked

54 citations

Joseph Glessner, Eleonora Porcu, Lisa‐Marie Niestroj, Jacob C. Ulirsch, Georgios Kellaris +28 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

Nature(2012)10.1038/nature11091

N/A

0.911DataRank · unranked

434 citations

Jason Willer, Michael E. Talkowski, Edwin C. Oh, Yu Taniguchi, Sébastien Jacquemont +10 more

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration

Human Molecular Genetics(2011)10.1093/hmg/ddr270

N/A

0.832DataRank · unranked

256 citations

Jesen Fagerness, Stephan Ripke, Gudmar Thorleifsson, Perciliz L. Tan, Eric H. Souied +50 more

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/362707

N/A

0.403DataRank · unranked

4 citations

Onuralp Söylemez, Aysegül Ozanturk, Sebastian Akle, Irwin Jungreis, Jean Muller +16 more

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome

Human Mutation(2020)10.1002/humu.24127

N/A

0DataRank · unranked

21 citations

Lokuliyange D. S. Senaratne, Elisabeth Ott, Asbjørn Holmgren, Dulika Sumathipala, Selma Mujezinović Larsen +25 more

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome

Clinical Genetics(2020)10.1111/cge.13878

N/A

0DataRank · unranked

26 citations

Samuel Nicaise, Manuela Antin, Anne‐Sophie Leuvrey, Elsa Nourisson, Carmen C. Leitch +22 more

Candidate variants in TUB are associated with familial tremor

PLoS Genetics(2020)10.1371/journal.pgen.1009010

N/A

0DataRank · unranked

4 citations

Fereshteh Jahanbani, Charles W. Abbott, Hayan Lee, Amin Zia, Shannon Rego +13 more

Gene expression elucidates functional impact of polygenic risk for schizophrenia

UNC Libraries(2020)10.17615/k6wj-s665

N/A

0DataRank · unranked

0 citations

Edwin C. Oh, Eli A. Stahl, David A. Bennett, Nicholas Katsanis, Tymor Hamamsy +53 more

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52

N/A

0DataRank · unranked

0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

Acoustofluidic rotational tweezing enables high-speed contactless morphological phenotyping of zebrafish larvae

Nature Communications(2021)10.1038/s41467-021-21373-3

N/A

0DataRank · unranked

102 citations

Yuyang Gu, Julien Philippe, Peiran Zhang, Hunter Bachman, Jinxin Zhang +7 more

Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.017

N/A

0DataRank · unranked

32 citations

Marie Vincent, Alice Mollé, Oluwadamilare A. Adebambo, Cynthia Fourgeux, Tahir Naeem Khan +41 more

Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations

Kidney International(2021)10.1016/j.kint.2021.09.034

N/A

0DataRank · unranked

27 citations

Dina Ahram, Yangfan P. Liu, Rik Westland, Rosemary V. Sampogna, Nicholas Katsanis +3 more

Dissecting the complexity of CNV pathogenicity: insights from Drosophila and zebrafish models

Current Opinion in Genetics & Development(2021)10.1016/j.gde.2021.02.013

N/A

0DataRank · unranked

4 citations

Georgios Kellaris, Santhosh Girirajan, Nicholas Katsanis, Tanzeen Yusuff

An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variants

JCI Insight(2024)10.1172/jci.insight.172475

N/A

0DataRank · unranked

4 citations

Carol Saunders, Marie-Françoise O’Donohue, David W. Reid, Kelsey McFadden, Nathalie Montel-Lehry +21 more

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

UNC Libraries(2024)10.17615/cwjg-e873

N/A

0DataRank · unranked

0 citations

Garrett M.E, Soldano K.L, Jeremiah Savage, Lawrence S Barak, Ashley-Koch A.E +14 more

CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module

Nature Communications(2020)10.1038/s41467-020-19113-0

N/A

0DataRank · unranked

99 citations

Katsutoshi Mizuno, Tabea Nöthe-Menchen, Yayoi Ikawa, Karsten Boldt, Asaf Ta‐Shma +46 more

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

Nature Communications(2020)10.1038/s41467-020-19637-5

N/A

0DataRank · unranked

34 citations

Melanie E. Garrett, Maria Kousi, Ramona M. Rodriguiz, Sungjin Moon, Yushi Bai +14 more

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Scientific Reports(2020)10.1038/s41598-020-58510-9

N/A

0DataRank · unranked

63 citations

Susette Lauwen, Christina Kiel, Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey +95 more

Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.005

N/A

0DataRank · unranked

55 citations

Xénia Latypova, Lokuliyanage Dona Samudita Senaratne, Ludovic Martin, Daniel C. Koboldt, Georgios Kellaris +72 more

TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

Human Molecular Genetics(2020)10.1093/hmg/ddaa120

N/A

0DataRank · unranked

22 citations

Ravikumar Balasubramanian, Zachary A Kupchinsky, David L. Keefe, Lacey Plummer, Kamal Khan +19 more

Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies

Human Molecular Genetics(2020)10.1093/hmg/ddaa073

N/A

0DataRank · unranked

19 citations

John N. Griffin, Thomas Arbogast, Tanner O. Monroe, Flavia Palombo, Marcella Martinelli +5 more

Nicholas Katsanis

Indexed papers

Top data-sharing exemplar

Papers