Publications by authors named "Igor Splawski"

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Complete loss of SLC30A8 in humans improves glucose metabolism and beta cell function.
Lindsey B Lamarche, Christopher Koch, Shareef Khalid, Maleeha Zaman Khan, Richard Zessis, Igor Splawski

Diabetologia· December 2025

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An ANGPTL4 inhibitory antibody safely improves lipid profiles in non-human primates.
Beryl B Cummings, Page R Bouchard, Mark N Milton, Peter F Moesta, Vyas Ramanan, Igor Splawski

EBioMedicine· July 2025

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Safety and efficacy of a novel ANGPTL4 inhibitory antibody for lipid lowering: results from phase 1 and phase 1b/2a clinical studies.
Beryl B Cummings, Mark P Joing, Page R Bouchard, Mark N Milton, Peter F Moesta, Igor Splawski

Lancet· May 2025

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Identification and characterization of human GDF15 knockouts.
Allan M Gurtan, Shareef Khalid, Christopher Koch, Maleeha Zaman Khan, Lindsey B Lamarche, Igor Splawski

Nat Metab· October 2024

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Tesidolumab (LFG316) for treatment of C5-variant patients with paroxysmal nocturnal hemoglobinuria.
Jun-Ichi Nishimura, Kiyoshi Ando, Masayoshi Masuko, Hideyoshi Noji, Yoshikazu Ito, Igor Splawski

Haematologica· June 2022

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TRPM1 forms ion channels associated with melanin content in melanocytes.
Elena Oancea, Joris Vriens, Sebastian Brauchi, Janice Jun, Igor Splawski

Sci Signal· May 2009

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Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndrome.
Niels Decher, Vijay Renigunta, Marylou Zuzarte, Malle Soom, Stefan H Heinemann, Igor Splawski

Cardiovasc Res· September 2007

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CACNA1H mutations in autism spectrum disorders.
Igor Splawski, Dana S Yoo, Stephanie C Stotz, Allison Cherry, David E Clapham

J Biol Chem· August 2006

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Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.
Igor Splawski, Katherine W Timothy, Niels Decher, Pradeep Kumar, Frank B Sachse

Proc Natl Acad Sci U S A· June 2005

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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing.
Michael J Ackerman, Igor Splawski, Jonathan C Makielski, David J Tester, Melissa L Will

Heart Rhythm· November 2004

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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar

Cell· October 2004

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An intronic mutation causes long QT syndrome.
Li Zhang, G Michael Vincent, Marco Baralle, Francisco E Baralle, Blake D Anson, Igor Splawski

J Am Coll Cardiol· September 2004

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A cardiac arrhythmia syndrome caused by loss of ankyrin-B function.
Peter J Mohler, Igor Splawski, Carlo Napolitano, Georgia Bottelli, Leah Sharpe

Proc Natl Acad Sci U S A· June 2004

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Compound mutations: a common cause of severe long-QT syndrome.
Peter Westenskow, Igor Splawski, Katherine W Timothy, Mark T Keating, Michael C Sanguinetti

Circulation· April 2004

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Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia.
Igor Splawski, Katherine W Timothy, Michihiro Tateyama, Colleen E Clancy, Alka Malhotra

Science· August 2002

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