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Hanns Lochmüller

ResearcherPublications, citations & collaboration network

Hanns Lochmüller is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Hanns Lochmüller have?

ScholarIQindexed works

Hanns Lochmüller has 1,557 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Hanns Lochmüller have?

ScholarIQcitation count

Hanns Lochmüller has 39,384 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Hanns Lochmüller?

ScholarIQh-index

Hanns Lochmüller has an h-index of 101 in OpenAlex.

What is the i10-index of Hanns Lochmüller?

ScholarIQi10-index

Hanns Lochmüller has an i10-index of 549 in OpenAlex.

What is the ORCID of Hanns Lochmüller?

ScholarIQorcid

The ORCID for Hanns Lochmüller is on the source record.

What is the OpenAlex record for Hanns Lochmüller?

ScholarIQopenalex

The OpenAlex for Hanns Lochmüller is on the source record.

What are the most-cited papers on Hanns Lochmüller?

ScholarIQmost cited works
The Human Phenotype Ontology in 2017
Sebastian Köhler, Nicole Vasilevsky, Mark Engelstad, Erin D. Foster, Julie A. McMurry, Ségolène Aymé, Gareth Baynam, Susan M. Bello, Cornelius F. Boerkoel, Kym M. Boycott, Michael Brudno, Orion J. Buske, Patrick F. Chinnery, Valentina Cipriani, Laureen E. Connell, Hugh Dawkins, Laura E. DeMare, A. Devereau, Bert B.A. de Vries, Helen V. Firth, Kathleen Freson, Daniel Greene, Ada Hamosh, Ingo Helbig, Courtney Hum, Johanna Jähn, Roger James, Roland Krause, Stanley J. F. Laulederkind, Hanns Lochmüller, Gholson J. Lyon, Soichi Ogishima, Annie Olry, Willem H. Ouwehand, Nikolas Pontikos, Ana Rath, Franz Schaefer, Richard H. Scott, Michael M. Segal, Panagiotis I. Sergouniotis, Richard Sever, Cynthia L. Smith, Volker Straub, Rachel Thompson, C. Turner, Ernest Turro, Marijcke W. M. Veltman, Tom Vulliamy, Jing Yu, Julie von Ziegenweidt, Andreas Zankl, Stephan Züchner, Tomasz Żemojtel, Julius O.B. Jacobsen, Tudor Groza, Damian Smedley, Chris Mungall, Melissa Haendel, Peter N. Robinson
Nucleic Acids Research. 2016816 CitationsOPEN ACCESS
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
Catherine L. Bladen, David Salgado, Soledad Monges, María Eugenia Foncuberta, Kyriaki Kekou, Konstantina Kosma, Hugh Dawkins, Leanne Lamont, Anna J. Roy, Teodora Chamova, Velina Guergueltcheva, H.S. Chan, Lawrence Korngut, Craig Campbell, Yi Dai, Jen Wang, Nina Barišić, Petr Brabec, Jaana Lähdetie, Maggie C. Walter, Olivia Schreiber‐Katz, Veronika Karcagi, Marta Garami, Venkatarman Viswanathan, Farhad Bayat, Filippo Buccella, En Kimura, Zaïda Koeks, J.C. van den Bergen, Miriam Rodrigues, Richard Roxburgh, Anna Łusakowska, Anna Kostera‐Pruszczyk, Janusz Zimowski, Rosário Santos, Elena Neagu, Svetlana Artemieva, Vedrana Milić Rašić, Dina Vojinović, Manuel Posada de la Paz, Clemens Bloetzer, P.Y. Jeannet, Franziska Joncourt, Jordi Díaz‐Manera, Eduard Gallardo, Ayşen Karaduman, Haluk Topaloğlu, Rasha El Sherif, Angela Stringer, Andriy Shatillo, Ann Martin, Holly L. Peay, M. Bellgard, Janbernd Kirschner, Kevin M. Flanigan, Volker Straub, Kate Bushby, Jan J.G.M. Verschuuren, Annemieke Aartsma‐Rus, Christophe Béroud, Hanns Lochmüller
Human Mutation. 2015753 CitationsOPEN ACCESS
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, Julius O.B. Jacobsen, Daniel Daniš, Jean-Philippe F. Gourdine, Michael Gargano, Nomi L. Harris, Nicolas Matentzoglu, Julie A. McMurry, David Osumi-Sutherland, Valentina Cipriani, James P. Balhoff, Tom Conlin, Hannah Blau, Gareth Baynam, R. Palmer, Dylan Gratian, Hugh Dawkins, Michael M. Segal, Anna Jansen, Ahmed Muaz, Willie Chang, Jenna Bergerson, Stanley J. F. Laulederkind, Zafer Yüksel, Sergi Beltrán, Alexandra F. Freeman, Panagiotis I. Sergouniotis, Daniel W. Durkin, Andrea L. Storm, Marc Hanauer, Michael Brudno, Susan M. Bello, Murat Sincan, Kayli Rageth, Matthew T. Wheeler, Renske Oegema, Halima Lourghi, Maria G. Della Rocca, Rachel Thompson, F Castellanos, James R. Priest, Charlotte Cunningham‐Rundles, Ayushi Hegde, Ruth C. Lovering, Catherine Hajek, Annie Olry, Luigi D. Notarangelo, Morgan Similuk, Xingmin Zhang, David Gómez‐Andrés, Hanns Lochmüller, Hélène Dollfus, Sergio D. Rosenzweig, Shruti Marwaha, Ana Rath, Kathleen E. Sullivan, Cynthia L. Smith, Joshua D. Milner, Dorothée Leroux, Cornelius F. Boerkoel, Amy D. Klion, Melody C. Carter, Tudor Groza, Damian Smedley, Melissa Haendel, Chris Mungall, Peter N. Robinson
Nucleic Acids Research. 2018739 CitationsOPEN ACCESS
Prevalence, incidence and carrier frequency of 5q–linked spinal muscular atrophy – a literature review
Ingrid E.C. Verhaart, Agata Robertson, Ian Wilson, Annemieke Aartsma‐Rus, Shona Cameron, Cynthia C. Jones, Suzanne F. Cook, Hanns Lochmüller
Orphanet Journal of Rare Diseases. 2017730 CitationsOPEN ACCESS
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases
Kym M. Boycott, Ana Rath, Jessica X. Chong, Taila Hartley, Fowzan S. Alkuraya, Gareth Baynam, Anthony J. Brookes, Michael Brudno, Ángel Carracedo, Johan T. den Dunnen, Stephanie O. M. Dyke, Xavier Estivill, Jack Goldblatt, Catherine Gonthier, Stephen C. Groft, Marta Gut, Ada Hamosh, Philip Hieter, Sophie Höhn, Matthew E. Hurles, Petra Kaufmann, Bartha Maria Knoppers, Jeffrey P. Krischer, Milan Maçek, Gert Matthijs, Annie Olry, Samantha Parker, Justin Paschall, Anthony Philippakis, Heidi L. Rehm, Peter N. Robinson, Pak C. Sham, Румен Стефанов, Domenica Taruscio, Divya Unni, Megan R. Vanstone, Feng Zhang, Han G. Brunner, Michael J. Bamshad, Hanns Lochmüller
The American Journal of Human Genetics. 2017465 CitationsOPEN ACCESS

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