ScholarIQanswers from OpenAlex
American Journal of Medical Genetics Part A
JournalCitation impact & published research
American Journal of Medical Genetics Part A is a journal indexed in ScholarIQ from OpenAlex.
How many works does American Journal of Medical Genetics Part A have?
ScholarIQindexed works
American Journal of Medical Genetics Part A has 13,243 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does American Journal of Medical Genetics Part A have?
ScholarIQcitation count
American Journal of Medical Genetics Part A has 311,334 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of American Journal of Medical Genetics Part A?
ScholarIQh-index
American Journal of Medical Genetics Part A has an h-index of 162 in OpenAlex.
What is the article processing charge of American Journal of Medical Genetics Part A?
ScholarIQarticle processing charge
American Journal of Medical Genetics Part A lists an article processing charge of 4,200 USD in OpenAlex.
What is the OpenAlex record for American Journal of Medical Genetics Part A?
ScholarIQopenalex
The OpenAlex for American Journal of Medical Genetics Part A is on the source record.
What are the most-cited papers on American Journal of Medical Genetics Part A?
ScholarIQmost cited works
Nosology and classification of genetic skeletal disorders: 2019 revision
Geert Mortier, Daniel H. Cohn, Valérie Cormier‐Daire, Christine M Hall, Deborah Krakow, Stefan Mundlos, Gen Nishimura, Stephen P. Robertson, Luca Sangiorgi, Ravi Savarirayan, David Sillence, Andrea Superti‐Furga, Sheila Unger, Matthew L. Warman
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>
Yanick J. Crow, Diana Chase, Johanna L. Schmidt, Marcin Szynkiewicz, Gabriella Forte, Hannah Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam, Sam Ackroyd, Alec Aeby, Guillermo Agosta, Catherine S. W. Albin, Stavit A. Shalev, Montse Arellano, Giada Ariaudo, Vijay Aswani, Riyana Babul‐Hirji, Eileen Baildam, Nadia Bahi‐Buisson, Kathryn Bailey, Christine Barnérias, Magalie Barth, Roberta Battini, Michael W. Beresford, Geneviève Bernard, Marika Bianchi, Thierry Billette de Villemeur, Edward Blair, Miriam Bloom, Alberto Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro‐Gago, Anna Cavallini, Cristina Cereda, Kate Chandler, David Chitayat, Abigail E. Collins, Concepción Sierra Córcoles, Nuno Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D’Arrigo, Christian G E L De Goede, Corinne De Laet, Liesbeth M. H. De Waele, Inés María Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Naz Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, P. Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming Lim, Jean‐Pierre Lin, Tarja Linnankivi, Mark T. Mackay, Daphna Marom, Charles Marques Lourenço, Shane McKee, Isabella Moroni, Jenny E.V. Morton, Marie‐Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemí Núñez‐Enamorado, P.J. Oades, Ivana Olivieri, John R. Østergaard, Belén Pérez‐Dueñas, Julie Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez
Nosology and classification of genetic skeletal disorders: 2015 revision
Luisa Bonafé, Valérie Cormier‐Daire, Christine M Hall, Ralph Lachman, Geert Mortier, Stefan Mundlos, Gen Nishimura, Luca Sangiorgi, Ravi Savarirayan, David Sillence, Jürgen W. Spranger, Andrea Superti‐Furga, Matthew L. Warman, Sheila Unger
<i>SOX2</i> anophthalmia syndrome
Nicola Ragge, Birgit Lorenz, Adele Schneider, Kate Bushby, Luisa De Sanctis, Ugo de Sanctis, Alison Salt, J. R. O. Collin, Anthony J. Vivian, S. L. Free, Pamela J. Thompson, Kathleen A. Williamson, Sanjay M. Sisodiya, Veronica van Heyningen, David Fitzpatrick
Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients
Chayim Schell-Apacik, Kristina Wagner, Moritz Bihler, Birgit Ertl‐Wagner, Uwe Heinrich, Eva Klopocki, Vera M. Kalscheuer, Maximilian Muenke, Hubertus von Voß