Adam Ameur

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 32

Top Venues

Nature communications

Genes

Communications biology

European journal of human genetics : EJHG

This page only lists publications with an associated author ORCID identifier.

Publications

Saskia Sydow, Paul Piccinelli, Shamik Mitra, Panagiotis Tsagkozis, Asle Charles Hesla, Camila B R De Mattos, Jan Köster, Linda Magnusson, Jenny Nilsson, Adam Ameur, Rene Wardenaar, Floris Foijer, Diana Carolina Johanna Spierings, Fredrik Mertens
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma. Communications biology 7 (1) (2024)
Wouter De Coster, Ida Höijer, Inge Bruggeman, Svenn D'Hert, Malin Melin, Adam Ameur, Rosa Rademakers
Visualization and analysis of medically relevant tandem repeats in nanopore sequencing of control cohorts with pathSTR. Genome research (2024)
Saskia Sydow, Paul Piccinelli, Shamik Mitra, Panagiotis Tsagkozis, Asle Charles Hesla, Camila B R De Mattos, Jan Köster, Linda Magnusson, Jenny Nilsson, Adam Ameur, Rene Wardenaar, Floris Foijer, Diana Carolina Johanna Spierings, Fredrik Mertens
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma. Communications biology 7 (1) (2024)
Saskia Sydow, Paul Piccinelli, Shamik Mitra, Panagiotis Tsagkozis, Asle Charles Hesla, Camila B R De Mattos, Jan Köster, Linda Magnusson, Jenny Nilsson, Adam Ameur, Rene Wardenaar, Floris Foijer, Diana Carolina Johanna Spierings, Fredrik Mertens
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma. Communications biology 7 (1) (2024)
Saskia Sydow, Paul Piccinelli, Shamik Mitra, Panagiotis Tsagkozis, Asle Charles Hesla, Camila B R De Mattos, Jan Köster, Linda Magnusson, Jenny Nilsson, Adam Ameur, Rene Wardenaar, Floris Foijer, Diana Carolina Johanna Spierings, Fredrik Mertens
MDM2 amplification in rod-shaped chromosomes provides clues to early stages of circularized gene amplification in liposarcoma. Communications biology 7 (1) (2024)
Mariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, Anders Lundmark, Amanda Raine, Yanara Marincevic-Zuniga, Henrik Gezelius, Anna Bremer, Lars Feuk, Adam Ameur, Jessica Nordlund
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing. Life science alliance 7 (8) (2024)
Mariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, Anders Lundmark, Amanda Raine, Yanara Marincevic-Zuniga, Henrik Gezelius, Anna Bremer, Lars Feuk, Adam Ameur, Jessica Nordlund
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing. Life science alliance 7 (8) (2024)
Kristine Bilgrav Saether, Jesper Eisfeldt, Jesse Bengtsson, Ming Yin Lun, Christopher M Grochowski, Medhat Mahmoud, Hsiao-Tuan Chao, Jill A Rosenfeld, Pengfei Liu, Jakob Schuy, Adam Ameur, null null, James Paul Hwang, Fritz J Sedlazeck, Weimin Bi, Ronit Marom, Ann Nordgren, Claudia M B Carvalho, Anna Lindstrand
Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversions. medRxiv : the preprint server for health sciences (2024)
Mariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, Anders Lundmark, Amanda Raine, Yanara Marincevic-Zuniga, Henrik Gezelius, Anna Bremer, Lars Feuk, Adam Ameur, Jessica Nordlund
A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing. Life science alliance 7 (8) (2024)
Kimberly Sturk-Andreaggi, Martin Bodner, Joseph D Ring, Adam Ameur, Ulf Gyllensten, Walther Parson, Charla Marshall, Marie Allen
Complete Mitochondrial DNA Genome Variation in the Swedish Population. Genes 14 (11) (2023)
Kristine Bilgrav Saether, Daniel Nilsson, Håkan Thonberg, Emma Tham, Adam Ameur, Jesper Eisfeldt, Anna Lindstrand
Transposable element insertions in 1000 Swedish individuals. PloS one 18 (7) (2023)
Joanna Hård, Jeff E Mold, Jesper Eisfeldt, Christian Tellgren-Roth, Susana Häggqvist, Ignas Bunikis, Orlando Contreras-Lopez, Chen-Shan Chin, Jessica Nordlund, Carl-Johan Rubin, Lars Feuk, Jakob Michaëlsson, Adam Ameur
Long-read whole-genome analysis of human single cells. Nature communications 14 (1) (2023)
Josefin Johansson, Sarah Lidéus, Carina Frykholm, Cecilia Gunnarsson, Filip Mihalič, Sanna Gudmundsson, Sara Ekvall, Anna-Maja Molin, Mai Pham, Mauno Vihinen, Kristina Lagerstedt-Robinson, Ann Nordgren, Per Jemth, Adam Ameur, Göran Annerén, Maria Wilbe, Marie-Louise Bondeson
Gustavson syndrome is caused by an in-frame deletion in RBMX associated with potentially disturbed SH3 domain interactions. European journal of human genetics : EJHG (2023)
Ida Höijer, Anastasia Emmanouilidou, Rebecka Östlund, Robin van Schendel, Selma Bozorgpana, Marcel Tijsterman, Lars Feuk, Ulf Gyllensten, Marcel den Hoed, Adam Ameur
CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations. Nature communications 13 (1) (2022)
Kimberly Sturk-Andreaggi, Joseph D Ring, Adam Ameur, Ulf Gyllensten, Martin Bodner, Walther Parson, Charla Marshall, Marie Allen
The Value of Whole-Genome Sequencing for Mitochondrial DNA Population Studies: Strategies and Criteria for Extracting High-Quality Mitogenome Haplotypes. International journal of molecular sciences 23 (4) (2022)
Josefin Johansson, Carina Frykholm, Katharina Ericson, Kalliopi Kazamia, Amanda Lindberg, Nancy Mulaiese, Geir Falck, Per-Erik Gustafsson, Sarah Lidéus, Sanna Gudmundsson, Adam Ameur, Marie-Louise Bondeson, Maria Wilbe
Loss of Nexilin function leads to a recessive lethal fetal cardiomyopathy characterized by cardiomegaly and endocardial fibroelastosis. American journal of medical genetics. Part A 188 (6) (2022)
Matthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti-Rodriguez, Robert Karlsson, Julien Bryois, Björn Nystedt, Adam Ameur, Anna K Kähler, NaEshia Ancalade, Martilias S Farrell, James J Crowley, Yun Li, Patrik K E Magnusson, Ulf Gyllensten, Christina M Hultman, Patrick F Sullivan, Jin P Szatkiewicz
Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature communications 13 (1) (2022)
Holger Weishaupt, Matko Čančer, Gabriela Rosén, Karl O Holmberg, Susana Häggqvist, Ignas Bunikis, Yiwen Jiang, Smitha Sreedharan, Ulf Gyllensten, Oren J Becher, Lene Uhrbom, Adam Ameur, Fredrik J Swartling
Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomas. Neuro-oncology (2022)
Zhe Wang, Andrew Emmerich, Nicolas J Pillon, Timothy M Moore, Daiane Hemerich, Marilyn C Cornelis, Eugenia Mazzaferro, Siacia Broos, Tarunveer S Ahluwalia, Traci M Bartz, Amy R Bentley, Lawrence F Bielak, Mike Chong, Audrey Y Chu, Diane Berry, Rajkumar Dorajoo, Nicole D Dueker, Elisa Kasbohm, Bjarke Feenstra, Mary F Feitosa, Christian Gieger, Mariaelisa Graff, Leanne M Hall, Toomas Haller, Fernando P Hartwig, David A Hillis, Ville Huikari, Nancy Heard-Costa, Christina Holzapfel, Anne U Jackson, Åsa Johansson, Anja Moltke Jørgensen, Marika A Kaakinen, Robert Karlsson, Kathleen F Kerr, Boram Kim, Chantal M Koolhaas, Zoltan Kutalik, Vasiliki Lagou, Penelope A Lind, Mattias Lorentzon, Leo-Pekka Lyytikäinen, Massimo Mangino, Christoph Metzendorf, Kristine R Monroe, Alexander Pacolet, Louis Pérusse, Rene Pool, Rebecca C Richmond, Natalia V Rivera, Sebastien Robiou-du-Pont, Katharina E Schraut, Christina-Alexandra Schulz, Heather M Stringham, Toshiko Tanaka, Alexander Teumer, Constance Turman, Peter J van der Most, Mathias Vanmunster, Frank J A van Rooij, Jana V van Vliet-Ostaptchouk, Xiaoshuai Zhang, Jing-Hua Zhao, Wei Zhao, Zhanna Balkhiyarova, Marie N Balslev-Harder, Sebastian E Baumeister, John Beilby, John Blangero, Dorret I Boomsma, Soren Brage, Peter S Braund, Jennifer A Brody, Marcel Bruinenberg, Ulf Ekelund, Ching-Ti Liu, John W Cole, Francis S Collins, L Adrienne Cupples, Tõnu Esko, Stefan Enroth, Jessica D Faul, Lindsay Fernandez-Rhodes, Alison E Fohner, Oscar H Franco, Tessel E Galesloot, Scott D Gordon, Niels Grarup, Catharina A Hartman, Gerardo Heiss, Jennie Hui, Thomas Illig, Russell Jago, Alan James, Peter K Joshi, Taeyeong Jung, Mika Kähönen, Tuomas O Kilpeläinen, Woon-Puay Koh, Ivana Kolcic, Peter P Kraft, Johanna Kuusisto, Lenore J Launer, Aihua Li, Allan Linneberg, Jian'an Luan, Pedro Marques Vidal, Sarah E Medland, Yuri Milaneschi, Arden Moscati, Bill Musk, Christopher P Nelson, Ilja M Nolte, Nancy L Pedersen, Annette Peters, Patricia A Peyser, Christine Power, Olli T Raitakari, Mägi Reedik, Alex P Reiner, Paul M Ridker, Igor Rudan, Kathy Ryan, Mark A Sarzynski, Laura J Scott, Robert A Scott, Stephen Sidney, Kristin Siggeirsdottir, Albert V Smith, Jennifer A Smith, Emily Sonestedt, Marin Strøm, E Shyong Tai, Koon K Teo, Barbara Thorand, Anke Tönjes, Angelo Tremblay, Andre G Uitterlinden, Jagadish Vangipurapu, Natasja van Schoor, Uwe Völker, Gonneke Willemsen, Kayleen Williams, Quenna Wong, Huichun Xu, Kristin L Young, Jian Min Yuan, M Carola Zillikens, Alan B Zonderman, Adam Ameur, Stefania Bandinelli, Joshua C Bis, Michael Boehnke, Claude Bouchard, Daniel I Chasman, George Davey Smith, Eco J C N de Geus, Louise Deldicque, Marcus Dörr, Michele K Evans, Luigi Ferruci, Myriam Fornage, Caroline Fox, Theodore Garland, Vilmundur Gudnason, Ulf Gyllensten, Torben Hansen, Caroline Hayward, Bernardo Lessa Horta, Elina Hyppӧnen, Marjo-Riitta Jarvelin, W Craig Johnson, Sharon L R Kardia, Lambertus A L M Kiemeney, Markku Laakso, Claudia Langenberg, Terho Lehtimäki, Loic Le Marchand, null null, Patrik K E Magnusson, Nicholas G Martin, Mads Melbye, Andres Metspalu, David Meyre, Kari E North, Claes Ohlsson, Albertine J Oldehinkel, Marju Orho-Melander, Guillaume Paré, Taesung Park, Oluf Pedersen, Brenda W J H Penninx, Tune H Pers, Ozren Polasek, Inga Prokopenko, Charles N Rotimi, Nilesh J Samani, Xueling S Sim, Harold Snieder, Thorkild I A Sørensen, Timothy D Spector, Nicholas John Timpson, Rob M van Dam, Nathalie van der Velde, Cornelia M van Duijn, Peter Vollenweider, Henry Völzke, Trudy G Voortman, Gérard Waeber, Nicholas J Wareham, David R Weir, Heinz-Erich Wichmann, James F Wilson, Andrea L Hevener, Anna Krook, Juleen R Zierath, Martine A I Thomis, Ruth J F Loos, Marcel den Hoed
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature genetics 54 (9) (2022)
Anne-Mai Ilumäe, Helen Post, Rodrigo Flores, Monika Karmin, Hovhannes Sahakyan, Mayukh Mondal, Francesco Montinaro, Lauri Saag, Concetta Bormans, Luisa Fernanda Sanchez, Adam Ameur, Ulf Gyllensten, Mart Kals, Reedik Mägi, Luca Pagani, Doron M Behar, Siiri Rootsi, Richard Villems
Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes. European journal of human genetics : EJHG 29 (10) (2021)
Benedikt von der Heyde, Anastasia Emmanouilidou, Eugenia Mazzaferro, Silvia Vicenzi, Ida Höijer, Tiffany Klingström, Sitaf Jumaa, Olga Dethlefsen, Harold Snieder, Eco J C N de Geus, Adam Ameur, Erik Ingelsson, Amin Allalou, Hannah L Brooke, Marcel den Hoed
Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approach. Scientific reports 10 (1) (2020)
Esben B Madsen, Ida Höijer, Thomas Kvist, Adam Ameur, Marie J Mikkelsen
Xdrop: Targeted sequencing of long DNA molecules from low input samples using droplet sorting. Human mutation 41 (9) (2020)
Nazeefa Fatima, Anna Petri, Ulf Gyllensten, Lars Feuk, Adam Ameur
Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes. Genes 11 (12) (2020)
Matthew Halvorsen, Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti-Rodriguez, Robert Karlsson, Julien Bryois, Björn Nystedt, Adam Ameur, Anna K Kähler, NaEshia Ancalade, Martilias S Farrell, James J Crowley, Yun Li, Patrik K E Magnusson, Ulf Gyllensten, Christina M Hultman, Patrick F Sullivan, Jin P Szatkiewicz
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia. Nature communications 11 (1) (2020)
Luís Nunes, Kristine Ø Aasebø, Lucy Mathot, Viktor Ljungström, Per-Henrik Edqvist, Magnus Sundström, Anca Dragomir, Per Pfeiffer, Adam Ameur, Frederik Pontén, Artur Mezheyeuski, Halfdan Sorbye, Tobias Sjöblom, Bengt Glimelius
Molecular characterization of a large unselected cohort of metastatic colorectal cancers in relation to primary tumor location, rare metastatic sites and prognosis. Acta oncologica (Stockholm, Sweden) 59 (4) (2020)
Mark Pinese, Paul A Lacaze, Emma M Rath, Andrew Stone, Marie-Jo Brion, Adam Ameur, Sini Nagpal, Clare Puttick, Shane Husson, Dmitry Degrave, Tina Navin Cristina, Vivian F S Kahl, Aaron L Statham, Robyn L Woods, John J McNeill, Moeen Riaz, Margo Barr, Mark R Nelson, Christopher M Reid, Anne M Murray, Raj C Shah, Rory Wolfe, Joshua R Atkins, Chantel Fitzsimmons, Heath M Cairns, Melissa J Green, Vaughan J Carr, Mark J Cowley, Hilda A Pickett, Paul A James, Joseph E Powell, Warren Kaplan, Greg Gibson, Ulf Gyllensten, Murray J Cairns, Martin McNamara, Marcel E Dinger, David M Thomas
The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly. Nature communications 11 (1) (2020)
Matthew S Hestand, Adam Ameur
The Versatility of SMRT Sequencing. Genes 10 (1) (2019)
Adam Ameur
Goodbye reference, hello genome graphs. Nature biotechnology 37 (8) (2019)
Jessika Nordin, Adam Ameur, Kerstin Lindblad-Toh, Ulf Gyllensten, Jennifer R S Meadows
SweHLA: the high confidence HLA typing bio-resource drawn from 1000 Swedish genomes. European journal of human genetics : EJHG 28 (5) (2019)
Ida Höijer, Yu-Chih Tsai, Tyson A Clark, Paul Kotturi, Niklas Dahl, Eva-Lena Stattin, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur
Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing. Human mutation 39 (9) (2018)
Adam Ameur, Huiwen Che, Marcel Martin, Ignas Bunikis, Johan Dahlberg, Ida Höijer, Susana Häggqvist, Francesco Vezzi, Jessica Nordlund, Pall Olason, Lars Feuk, Ulf Gyllensten
De Novo Assembly of Two Swedish Genomes Reveals Missing Segments from the Human GRCh38 Reference and Improves Variant Calling of Population-Scale Sequencing Data. Genes 9 (10) (2018)
Ammar Zaghlool, Adam Ameur, Chenglin Wu, Jakub Orzechowski Westholm, Adnan Niazi, Manimozhi Manivannan, Kelli Bramlett, Mats Nilsson, Lars Feuk
Expression profiling and in situ screening of circular RNAs in human tissues. Scientific reports 8 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Adam Ameur