Joris A Veltman (J A Veltman)

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 25

Top Venues

Nature communications

Human mutation

Nature reviews. Urology

Genetics in medicine : official journal of the American College of Medical Genetics

Newcastle University

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

Affiliation History

Newcastle University Nov 01 2019

United Kingdom

Dean :: Biosciences Institute

Radboudumc Sep 01 2000 - Jan 31 2020

Netherlands

Head Research Division, prof.dr. :: Human Genetics

Newcastle University Feb 01 2017 - Oct 31 2019

United Kingdom

Director Institute :: Institute of Genetic Medicine

Publications

Joris A Veltman, Frank Tüttelmann
Why geneticists should care about male infertility. Nature reviews. Genetics (2024)
Christopher J De Jonge, Christopher L R Barratt, Robert John Aitken, Richard A Anderson, Peter Baker, David Yiu Leung Chan, Mark P Connolly, Michael L Eisenberg, Nicolas Garrido, Niels Jørgensen, Sarah Kimmins, Csilla Krausz, Robert I McLachlan, Craig Niederberger, Brendan J Houston, Allan A Pacey, Laerke Priskorn, Satu Rautakallio-Hokkanen, Gamal Serour, Joris A Veltman, Donna L Vogel, Mónica Hebe Vazquez-Levin
Current global status of male reproductive health. Human reproduction open 2024 (2) (2024)
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Luisa Meier, Ansgar Zoch, David MacKenzie MacLeod, Johanna Steingröver, Özlem Okutman, Daniela Fietz, Adrian M E Pilatz, Antoni Riera-Escamilla, Miguel J Xavier, Christian Ruckert, Sara Di Persio, Nina Neuhaus, Ali Sami Gurbuz, Ahmet Şalvarci, Nicolas Le May, Kevin McEleny, Corinna Friedrich, Godfried W van der Heijden, Margot J Wyrwoll, Sabine Kliesch, Joris A Veltman, Csilla Krausz, Stéphane Viville, Donald F Conrad, Dònal O' Carroll, Frank Tüttelmann
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. Nature communications 15 (1) (2024)
Christopher J De Jonge, Christopher L R Barratt, Robert John Aitken, Richard A Anderson, Peter Baker, David Yiu Leung Chan, Mark P Connolly, Michael L Eisenberg, Nicolas Garrido, Niels Jørgensen, Sarah Kimmins, Csilla Krausz, Robert I McLachlan, Craig Niederberger, Brendan J Houston, Allan A Pacey, Laerke Priskorn, Satu Rautakallio-Hokkanen, Gamal Serour, Joris A Veltman, Donna L Vogel, Mónica Hebe Vazquez-Levin
Current global status of male reproductive health. Human reproduction open 2024 (2) (2024)
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Luisa Meier, Ansgar Zoch, David MacKenzie MacLeod, Johanna Steingröver, Özlem Okutman, Daniela Fietz, Adrian M E Pilatz, Antoni Riera-Escamilla, Miguel J Xavier, Christian Ruckert, Sara Di Persio, Nina Neuhaus, Ali Sami Gurbuz, Ahmet Şalvarci, Nicolas Le May, Kevin McEleny, Corinna Friedrich, Godfried W van der Heijden, Margot J Wyrwoll, Sabine Kliesch, Joris A Veltman, Csilla Krausz, Stéphane Viville, Donald F Conrad, Dònal O' Carroll, Frank Tüttelmann
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. Nature communications 15 (1) (2024)
Birgit Stallmeyer, Clara Bühlmann, Rytis Stakaitis, Ann-Kristin Dicke, Farah Ghieh, Luisa Meier, Ansgar Zoch, David MacKenzie MacLeod, Johanna Steingröver, Özlem Okutman, Daniela Fietz, Adrian M E Pilatz, Antoni Riera-Escamilla, Miguel J Xavier, Christian Ruckert, Sara Di Persio, Nina Neuhaus, Ali Sami Gurbuz, Ahmet Şalvarci, Nicolas Le May, Kevin McEleny, Corinna Friedrich, Godfried W van der Heijden, Margot J Wyrwoll, Sabine Kliesch, Joris A Veltman, Csilla Krausz, Stéphane Viville, Donald F Conrad, Dònal O' Carroll, Frank Tüttelmann
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility. Nature communications 15 (1) (2024)
Margot Julia Wyrwoll, Godfried W van der Heijden, Csilla Krausz, Kenneth Ivan Aston, Sabine Kliesch, Robert McLachlan, Liliana Ramos, Donald F Conrad, Brendan J Houston, Joris A Veltman, Frank Tüttelmann
Improved phenotypic classification of male infertility to promote discovery of genetic causes. Nature reviews. Urology (2023)
Sarah Kimmins, Richard A Anderson, Christopher L R Barratt, Hermann M Behre, Sarah R Catford, Christopher J De Jonge, Géraldine Delbes, Michael L Eisenberg, Nicolás Garrido, Brendan J Houston, Niels Jørgensen, Csilla Krausz, Ariane Lismer, Robert I McLachlan, Suks Minhas, Tim Moss, Allan A Pacey, Laerke Priskorn, Stefan Schlatt, Jacquetta Trasler, Leonardo Trasande, Frank Tüttelmann, Mónica Hebe Vazquez-Levin, Joris A Veltman, Feng Zhang, Brendan J Houston
Frequency, morbidity and equity - the case for increased research on male fertility. Nature reviews. Urology (2023)
Manon S Oud, R M Smits, H E Smith, F Kumara Mastrorosa, G S Holt, B J Houston, P F de Vries, B K S Alobaidi, L E Batty, H Ismail, J Greenwood, Harsh J Sheth, A Mikulasova, G D N Astuti, Christian Gilissen, K McEleny, H Turner, Jonathan M Coxhead, S Cockell, Didi D M Braat, K Fleischer, K W M D'Hauwers, E Schaafsma, null null, Liina Nagirnaja, Donald F Conrad, C Friedrich, Sabine Kliesch, K I Aston, A Riera-Escamilla, C Krausz, C Gonzaga-Jauregui, M Santibanez-Koref, D J Elliott, Lisenka E L M Vissers, Frank Tüttelmann, Brendan J Houston, Liliana Ramos, Miguel J Xavier, Godfried W van der Heijden, Joris A Veltman
A de novo paradigm for male infertility. Nature communications 13 (1) (2022)
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Stakaitiene, Alexandra M Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka Vigh-Conrad, Manon S Oud, Miguel J Xavier, Samuel R Cheers, Emma R James, Jingtao Guo, Timothy G Jenkins, Antoni Riera-Escamilla, Alberto Barros, Filipa Carvalho, Susana Fernandes, João Gonçalves, Christina A Gurnett, Niels Jørgensen, Davor Jezek, Emily S Jungheim, Sabine Kliesch, Robert I McLachlan, Kenan R Omurtag, Adrian Pilatz, Jay I Sandlow, James Smith, Michael L Eisenberg, James M Hotaling, Keith A Jarvi, Margus Punab, Ewa Rajpert-De Meyts, Douglas T Carrell, Csilla Krausz, Maris Laan, Brendan J Houston, Peter N Schlegel, Frank Tüttelmann, Joris A Veltman, Kristian Almstrup, Kenneth I Aston, Donald F Conrad
Diverse monogenic subforms of human spermatogenic failure. Nature communications 13 (1) (2022)
R M Smits, Miguel J Xavier, Manon S Oud, G D N Astuti, A M Meijerink, P F de Vries, G S Holt, B K S Alobaidi, L E Batty, G Khazeeva, K Sablauskas, L E L M Vissers, C Gilissen, K Fleischer, D D M Braat, L Ramos, Joris A Veltman
De novo mutations in children born after medical assisted reproduction. Human reproduction (Oxford, England) 37 (6) (2022)
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Stakaitiene, Alexandra M Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka Vigh-Conrad, Manon S Oud, Miguel J Xavier, Samuel R Cheers, Emma R James, Jingtao Guo, Timothy G Jenkins, Antoni Riera-Escamilla, Alberto Barros, Filipa Carvalho, Susana Fernandes, João Gonçalves, Christina A Gurnett, Niels Jørgensen, Davor Jezek, Emily S Jungheim, Sabine Kliesch, Robert I McLachlan, Kenan R Omurtag, Adrian Pilatz, Jay I Sandlow, James Smith, Michael L Eisenberg, James M Hotaling, Keith A Jarvi, Margus Punab, Ewa Rajpert-De Meyts, Douglas T Carrell, Csilla Krausz, Maris Laan, Brendan J Houston, Peter N Schlegel, Frank Tüttelmann, Joris A Veltman, Kristian Almstrup, Kenneth I Aston, Donald F Conrad
Diverse monogenic subforms of human spermatogenic failure. Nature communications 13 (1) (2022)
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Stakaitiene, Alexandra M Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka Vigh-Conrad, Manon S Oud, Miguel J Xavier, Samuel R Cheers, Emma R James, Jingtao Guo, Timothy G Jenkins, Antoni Riera-Escamilla, Alberto Barros, Filipa Carvalho, Susana Fernandes, João Gonçalves, Christina A Gurnett, Niels Jørgensen, Davor Jezek, Emily S Jungheim, Sabine Kliesch, Robert I McLachlan, Kenan R Omurtag, Adrian Pilatz, Jay I Sandlow, James Smith, Michael L Eisenberg, James M Hotaling, Keith A Jarvi, Margus Punab, Ewa Rajpert-De Meyts, Douglas T Carrell, Csilla Krausz, Maris Laan, Brendan J Houston, Peter N Schlegel, Frank Tüttelmann, Joris A Veltman, Kristian Almstrup, Kenneth I Aston, Donald F Conrad
Diverse monogenic subforms of human spermatogenic failure. Nature communications 13 (1) (2022)
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Stakaitiene, Alexandra M Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka Vigh-Conrad, Manon S Oud, Miguel J Xavier, Samuel R Cheers, Emma R James, Jingtao Guo, Timothy G Jenkins, Antoni Riera-Escamilla, Alberto Barros, Filipa Carvalho, Susana Fernandes, João Gonçalves, Christina A Gurnett, Niels Jørgensen, Davor Jezek, Emily S Jungheim, Sabine Kliesch, Robert I McLachlan, Kenan R Omurtag, Adrian Pilatz, Jay I Sandlow, James Smith, Michael L Eisenberg, James M Hotaling, Keith A Jarvi, Margus Punab, Ewa Rajpert-De Meyts, Douglas T Carrell, Csilla Krausz, Maris Laan, Brendan J Houston, Peter N Schlegel, Frank Tüttelmann, Joris A Veltman, Kristian Almstrup, Kenneth I Aston, Donald F Conrad
Diverse monogenic subforms of human spermatogenic failure. Nature communications 13 (1) (2022)
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Stakaitiene, Alexandra M Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka Vigh-Conrad, Manon S Oud, Miguel J Xavier, Samuel R Cheers, Emma R James, Jingtao Guo, Timothy G Jenkins, Antoni Riera-Escamilla, Alberto Barros, Filipa Carvalho, Susana Fernandes, João Gonçalves, Christina A Gurnett, Niels Jørgensen, Davor Jezek, Emily S Jungheim, Sabine Kliesch, Robert I McLachlan, Kenan R Omurtag, Adrian Pilatz, Jay I Sandlow, James Smith, Michael L Eisenberg, James M Hotaling, Keith A Jarvi, Margus Punab, Ewa Rajpert-De Meyts, Douglas T Carrell, Csilla Krausz, Maris Laan, Brendan J Houston, Peter N Schlegel, Frank Tüttelmann, Joris A Veltman, Kristian Almstrup, Kenneth I Aston, Donald F Conrad
Diverse monogenic subforms of human spermatogenic failure. Nature communications 13 (1) (2022)
Liina Nagirnaja, Alexandra M Lopes, Wu-Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Stakaitiene, Alexandra M Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka Vigh-Conrad, Manon S Oud, Miguel J Xavier, Samuel R Cheers, Emma R James, Jingtao Guo, Timothy G Jenkins, Antoni Riera-Escamilla, Alberto Barros, Filipa Carvalho, Susana Fernandes, João Gonçalves, Christina A Gurnett, Niels Jørgensen, Davor Jezek, Emily S Jungheim, Sabine Kliesch, Robert I McLachlan, Kenan R Omurtag, Adrian Pilatz, Jay I Sandlow, James Smith, Michael L Eisenberg, James M Hotaling, Keith A Jarvi, Margus Punab, Ewa Rajpert-De Meyts, Douglas T Carrell, Csilla Krausz, Maris Laan, Brendan J Houston, Peter N Schlegel, Frank Tüttelmann, Joris A Veltman, Kristian Almstrup, Kenneth I Aston, Donald F Conrad
Diverse monogenic subforms of human spermatogenic failure. Nature communications 13 (1) (2022)
Giles S Holt, Lois E Batty, Bilal K S Alobaidi, Hannah E Smith, Manon S Oud, Liliana Ramos, Miguel J Xavier, Joris A Veltman
Phasing of de novo mutations using a scaled-up multiple amplicon long-read sequencing approach. Human mutation 43 (11) (2022)
Brendan J Houston, Manon S Oud, Daniel M Aguirre, D Jo Merriner, Anne E O'Connor, Özlem Okutman, Stéphane Viville, Richard Burke, Joris A Veltman, Brendan J Houston
Programmed Cell Death 2-Like (Pdcd2l) Is Required for Mouse Embryonic Development. G3 (Bethesda, Md.) 10 (12) (2020)
Miguel J Xavier, Albert Salas-Huetos, Manon S Oud, Kenneth Ivan Aston, Joris A Veltman
Disease gene discovery in male infertility: past, present and future. Human genetics 140 (1) (2020)
Simone Lipinski, Britt-Sabina Petersen, Matthias Barann, Agnes Piecyk, Florian Tran, Gabriele Mayr, Marlene Jentzsch, Konrad Aden, Stephanie T Stengel, Ulrich C Klostermeier, Vrunda Sheth, David Ellinghaus, Tobias Rausch, Jan O Korbel, Michael Nothnagel, Michael Krawczak, Christian Gilissen, Joris A Veltman, Michael J Forster, Peter Forster, Clarence C Lee, Annette Fritscher-Ravens, Stefan Schreiber, Andre Franke, Philip C Rosenstiel
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2. Cold Spring Harbor molecular case studies 5 (1) (2019)
Manon S Oud, Liliana Ramos, Moira K O'Bryan, Robert I McLachlan, Özlem Okutman, Stephane Viville, Petra F de Vries, Dominique F C M Smeets, Dorien Lugtenberg, Jayne Y Hehir-Kwa, Christian Gilissen, Maartje van de Vorst, Lisenka E L M Vissers, Alexander Hoischen, Aukje M Meijerink, Kathrin Fleischer, Joris A Veltman, Michiel J Noordam
Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Human mutation 38 (11) (2017)
Gaël Nicolas, Camille Charbonnier, Dominique Campion, Joris A Veltman
Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 177 (1) (2017)
Laurens Wiel, Hanka Venselaar, Joris A Veltman, Gert Vriend, Christian Gilissen
Aggregation of population-based genetic variation over protein domain homologues and its potential use in genetic diagnostics. Human mutation 38 (11) (2017)
Lisenka E L M Vissers, Kirsten J M van Nimwegen, Jolanda H Schieving, Erik-Jan Kamsteeg, Tjitske Kleefstra, Helger G Yntema, Rolph Pfundt, Gert Jan van der Wilt, Gert Jan van der Wilt, Han G Brunner, Simone van der Burg, Janneke Grutters, Joris A Veltman, Michèl A A P Willemsen
A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology. Genetics in medicine : official journal of the American College of Medical Genetics 19 (9) (2017)
Rolph Pfundt, Marisol Del Rosario, Lisenka E L M Vissers, Michael P Kwint, Irene M Janssen, Nicole de Leeuw, Helger G Yntema, Marcel R Nelen, Dorien Lugtenberg, Erik-Jan Kamsteeg, Nienke Wieskamp, Alexander P A Stegmann, Servi J C Stevens, Richard J T Rodenburg, Annet Simons, Arjen R Mensenkamp, Tuula Rinne, Christian Gilissen, Hans Scheffer, Joris A Veltman, Jayne Y Hehir-Kwa
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders. Genetics in medicine : official journal of the American College of Medical Genetics 19 (6) (2016)

Joris A Veltman.css-eqlu8i{font-size:small;padding-left:4px;} (J A Veltman)

Publication Activity (10 Years)

Top Topics

Top Venues

Joris A Veltman (J A Veltman)