Hans T. Björnsson

Also affiliated with Johns Hopkins University, University of Iceland, National University Hospital of Iceland

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 30 papers. Top paper: “Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation”.

Leveraging the Mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation

eLife(2021)10.7554/elife.65884

N/A

0.795DataRank · unranked

31 citations

Leandros Boukas, Li Zhang, Genay Pilarowski, Jenny Jiang, Allison Kalinousky +3 more

Universal prediction of cell-cycle position using transfer learning

Genome biology(2022)10.1186/s13059-021-02581-y

N/A

0.735DataRank · unranked

133 citations

Genevieve L. Stein-O’Brien, Jonathan J. Augustin, Jared Slosberg, Giovanni A. Carosso, Briana L. Winer +5 more

A mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibition

JCI Insight(2023)10.1172/jci.insight.173392

N/A

0.640DataRank · unranked

20 citations

Wanying Lin, Ryan C. Riddle, Priyanka Kushwaha, Leandros Boukas, Hans T. Björnsson +3 more

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.002

N/A

0.568DataRank · unranked

43 citations

Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong +95 more

An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.014

N/A

0.546DataRank · unranked

37 citations

Vanda McNiven, Cheryl Cytrynbaum, Maryam Jangjoo, Margaret P Adam, Hans T. Björnsson +57 more

Individuals with Wiedemann-Steiner syndrome show nonverbal reasoning and visuospatial defects with relative verbal skill sparing

Journal of the International Neuropsychological Society(2022)10.1017/s1355617722000467

N/A

0.442DataRank · unranked

18 citations

Jacqueline Harris, Jill A. Fahrner, Hans T. Björnsson, Rowena Ng

Universal prediction of cell cycle position using transfer learning

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.06.438463

N/A

0.406DataRank · unranked

14 citations

Genevieve L. Stein-O’Brien, Jonathan J. Augustin, Jared Slosberg, Giovanni A. Carosso, Briana L. Winer +5 more

Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2

PLoS Genetics(2022)10.1371/journal.pgen.1010278

N/A

0.396DataRank · unranked

13 citations

Kimberley Jade Anderson, Leandros Boukas, Hans T. Björnsson, Tinna Reynisdottir

Inhibition of KDM1A activity restores adult neurogenesis and improves hippocampal memory in a mouse model of Kabuki syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.11.986976

N/A

0.280DataRank · unranked

4 citations

Genay Pilarowski, Emilio Merlo Pich, Atsushi Nakatani, John Dunlop, Rina Baba +8 more

KMT2D Deficiency Causes Sensorineural Hearing Loss in Mice and Humans

Genes(2023)10.3390/genes15010048

N/A

0.218DataRank · unranked

2 citations

Teresa Romeo Luperchio, Katrina M. Schrode, Jacqueline Harris, Li Zhang, Valerie B. DeLeon +4 more

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

medRxiv(2025)10.1101/2025.05.06.25326635

N/A

0.165DataRank · unranked

2 citations

Eirny Tholl Thorolfsdottir, Ilana M. Nodelman, Sara Tholl Halldorsdottir, Stefania Benónísdóttir, Malak Alghamdi +64 more

Neuron-specific chromatin disruption at CpG islands and aging-related regions in Kabuki syndrome mice

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.01.551456

N/A

0.165DataRank · unranked

2 citations

Teresa Romeo Luperchio, Afrooz Razi, Kasper D. Hansen, Hans T. Björnsson, Leandros Boukas

In-utero rescue of neurological dysfunction in a mouse model of Wiedemann-Steiner syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.07.19.604339

N/A

0.104DataRank · unranked

1 citations

Kimberley Jade Anderson, Andrew Brinn, Katheryn P. Franklin, Juan Ouyang, Ásbjörg Ósk Snorradóttir +5 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner Syndrome

Molecular Genetics and Metabolism(2021)10.1016/s1096-7192(21)00373-5

N/A

0.104DataRank · unranked

1 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more

Promoter CpG density predicts downstream gene loss-of-function intolerance

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.15.936351

N/A

0DataRank · unranked

0 citations

Hans T. Björnsson, Kasper D. Hansen, Leandros Boukas

Leveraging the Mendelian Disorders of the Epigenetic Machinery to Systematically Map Functional Epigenetic Variation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.08.373456

N/A

0DataRank · unranked

1 citations

Leandros Boukas, Zhang Li, Genay Pilarowski, Jenny Jiang, Allison Kalinousky +3 more

Neurobehavioral phenotype of Kabuki syndrome: Anxiety is a common feature

Frontiers in Genetics(2022)10.3389/fgene.2022.1007046

N/A

0DataRank · unranked

16 citations

Tyler Rapp, Hadia Hijazi, Jennifer Johnson, Hans T. Björnsson, Jacqueline Harris +1 more

Natural selection acts on epigenetic marks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.04.187880

N/A

0DataRank · unranked

10 citations

Afrooz Razi, Hans T. Björnsson, Kasper D. Hansen, Leandros Boukas

Sleep disturbances correlate with behavioral problems among individuals with Wiedemann-Steiner syndrome

Frontiers in Genetics(2022)10.3389/fgene.2022.950082

N/A

0DataRank · unranked

7 citations

Hans T. Björnsson, Jill A. Fahrner, Jacqueline Harris, Rowena Ng

Untargeted metabolomics as an unbiased approach to the diagnosis of inborn errors of metabolism of the non-oxidative branch of the pentose phosphate pathway

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.07.013

N/A

0DataRank · unranked

24 citations

Taraka Donti, Jing Xiao, Charul Gijavanekar, Adam D. Kennedy, Leroy Hubert +11 more

The social phenotype associated with Wiedemann‐Steiner syndrome: Autistic traits juxtaposed with high social drive and prosociality

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63351

N/A

0DataRank · unranked

6 citations

Allison Kalinousky, Jill A. Fahrner, Hans T. Björnsson, Jacqueline Harris, Rowena Ng

Inhibition of KDM1A activity restores adult neurogenesis and improves hippocampal memory in a mouse model of Kabuki syndrome

Molecular Therapy — Methods & Clinical Development(2021)10.1016/j.omtm.2021.02.011

N/A

0DataRank · unranked

47 citations

Genay Pilarowski, Emilio Merlo Pich, Atsushi Nakatani, John Dunlop, Rina Baba +8 more

Promoter CpG Density Predicts Downstream Gene Loss-of-Function Intolerance

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.07.014

N/A

0DataRank · unranked

17 citations

Hans T. Björnsson, Kasper D. Hansen, Leandros Boukas

SMYD5 is a regulator of the mild hypothermia response

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.11.540170

N/A

0DataRank · unranked

0 citations

ki-jin jang, Sara Tholl Halldorsdottir, Meghna Vinod, Arnhildur Tomasdottir, Katrín Möller +13 more

SMYD5 is a regulator of the mild hypothermia response

Cell Reports(2024)10.1016/j.celrep.2024.114554

N/A

0DataRank · unranked

6 citations

ki-jin jang, Sara Tholl Halldorsdottir, Meghna Vinod, Arnhildur Tomasdottir, Katrín Möller +13 more

Growth deficiency in a mouse model of Kabuki syndrome 2 bears mechanistic similarities to Kabuki syndrome 1

PLoS Genetics(2024)10.1371/journal.pgen.1011310

N/A

0DataRank · unranked

4 citations

Wanying Lin, Ryan C. Riddle, Sheetal Chopra, Jiyoung Kim, Leandros Boukas +4 more

Neuron-specific chromatin disruption at CpG islands and aging-related regions in Kabuki syndrome mice

Genome Research(2024)10.1101/gr.278416.123

N/A

0DataRank · unranked

3 citations

Teresa Romeo Luperchio, Afrooz Razi, Kasper D. Hansen, Hans T. Björnsson, Leandros Boukas

In utero rescue of neurological dysfunction in a mouse model of Wiedemann-Steiner syndrome

JCI Insight(2025)10.1172/jci.insight.187039

N/A

0DataRank · unranked

2 citations

Kimberley Jade Anderson, Katrín Möller, Stefán Pétursson, Andrew Brinn, Katheryn P. Franklin +7 more

Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance

Journal of Clinical Immunology(2020)10.1007/s10875-020-00817-3

N/A

0DataRank · unranked

40 citations

Qing Zhou, Natalia Sampaio Moura, Amanda K. Ombrello, Drew G. Michael, Natalie Deuitch +15 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62124

N/A

0DataRank · unranked

72 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more