ScholarIQanswers from OpenAlex & ORCID
Kimberly Gilmour
ResearcherPublications, citations & collaboration network
Kimberly Gilmour is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Kimberly Gilmour have?
ScholarIQindexed works
Kimberly Gilmour has 280 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Kimberly Gilmour have?
ScholarIQcitation count
Kimberly Gilmour has 20,831 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Kimberly Gilmour?
ScholarIQh-index
Kimberly Gilmour has an h-index of 65 in OpenAlex.
What is the i10-index of Kimberly Gilmour?
ScholarIQi10-index
Kimberly Gilmour has an i10-index of 160 in OpenAlex.
What is the ORCID of Kimberly Gilmour?
ScholarIQorcid
The ORCID for Kimberly Gilmour is on the source record.
What is the OpenAlex record for Kimberly Gilmour?
ScholarIQopenalex
The OpenAlex for Kimberly Gilmour is on the source record.
What are the most-cited papers on Kimberly Gilmour?
ScholarIQmost cited works
Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development
Florian Otto, Anders Thornell, Tessa Crompton, Angela Denzel, Kimberly Gilmour, Ian Rosewell, Gordon Stamp, Rosa Beddington, Stefan Mundlos, Bjørn R. Olsen, Paul B. Selby, Michael J. Owen
The Human Phenotype Ontology in 2024: phenotypes around the world
Michael Gargano, Nicolas Matentzoglu, Ben Coleman, Eunice B Addo-Lartey, Anna V. Anagnostopoulos, Joel Anderton, Paul Avillach, Anita Bagley, Eduard Bakštein, James P. Balhoff, Gareth Baynam, Susan M. Bello, Michael Berk, Holli Bertram, Somer Bishop, Hannah Blau, David F. Bodenstein, Pablo Botas, Kaan Boztuǧ, J Cady, Tiffany J. Callahan, Rhiannon Cameron, Seth Carbon, F Castellanos, J. Harry Caufield, Lauren Chan, Christopher G. Chute, Jaime Cruz-Rojo, Noémi Dahan‐Oliel, Jon R. Davids, Maud de Dieuleveult, Vinícius de Souza, Bert B.A. de Vries, Esther de Vries, J. Raymond DePaulo, Beáta Dérfalvi, Ferdinand Dhombres, Claudia Diaz‐Byrd, Alexander J.M. Dingemans, Bruno Donadille, Michael Duyzend, Reem Elfeky, Shahim Essaid, Carolina Fabrizzi, Giovanna Fico, Helen V. Firth, Yun Freudenberg‐Hua, Janice M. Fullerton, Davera Gabriel, Kimberly Gilmour, Jessica L. Giordano, Fernando S. Goes, Rachel Gore Moses, Ian Green, Matthias Griese, Tudor Groza, Weihong Gu, Julia Guthrie, Benjamin M. Gyori, Ada Hamosh, Marc Hanauer, Kateřina Hanušová, Yongqun He, Harshad Hegde, Ingo Helbig, Kateřina Holasová, Charles Tapley Hoyt, Shangzhi Huang, Eric Hurwitz, Julius O.B. Jacobsen, Xiaofeng Jiang, Lisa Joseph, Kamyar Keramatian, Bryan King, Katrin Knoflach, David A. Koolen, Megan L Kraus, Carlo Kroll, Maaike Kusters, Markus S. Ladewig, David Lagorce, Meng‐Chuan Lai, Pablo Lapunzina, Bryan Laraway, David Lewis‐Smith, Xiarong Li, Caterina Lucano, Marzieh Majd, Mary L. Marazita, Víctor Martínez‐Glez, Toby H McHenry, Melvin G. McInnis, Julie A. McMurry, Michaela Mihulová, Caitlin E. Millett, Philip B. Mitchell, Veronika Moslerová, Kenji Narutomi, Shahrzad Nematollahi, Julián Nevado
Whole-genome sequencing of a sporadic primary immunodeficiency cohort
James Thaventhiran, Hana Lango Allen, Oliver S. Burren, William Rae, Daniel Greene, Emily Staples, Zinan Zhang, James H. R. Farmery, Ilenia Simeoni, Elizabeth Rivers, Jesmeen Maimaris, Christopher J. Penkett, Jonathan Stephens, Sri V. V. Deevi, Alba Sanchis‐Juan, Nicholas Gleadall, Moira Thomas, Ravishankar Sargur, Pavels Gordins, Helen E. Baxendale, Matthew A. Brown, Paul Tuijnenburg, Austen Worth, Steven Hanson, Rachel Linger, Matthew Buckland, Paula Rayner-Matthews, Kimberly Gilmour, Crina Samarghitean, Suranjith L. Seneviratne, David M. Sansom, Andy G. Lynch, Karyn Mégy, Eva Ellinghaus, David Ellinghaus, Silje F. Jørgensen, Tom H. Karlsen, Kathleen Stirrups, Antony J. Cutler, Dinakantha Kumararatne, Anita Chandra, David Edgar, Archana Herwadkar, Nichola Cooper, Sofia Grigoriadou, Aarnoud Huissoon, Sarah Goddard, Stephen Jolles, Catharina Schuetz, Felix Boschann, Stephen Abbs, Zoe Adhya, Julian Adlard, Maryam Afzal, Irshad Ahmed, Munaza Ahmed, Saeed Ahmed, Timothy J. Aitman, Hana Alachkar, Jayanthi Alamelu, Raza Alikhan, Carl E. Allen, Louise Allen, David Allsup, Arif Alvi, Gautam Ambegaonkar, Ariharan Anantharachagan, Philip Ancliff, Julie A. Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Rita Arya, Sofie Ashford, William J. Astle, Anthony Attwood, Steve Austin, Yeşim Aydınok, Waqar Ayub, Christian Babbs, Chiara Bacchelli, Trevor Baglin, Tamam Bakchoul, Tadbir K. Bariana, Jonathan Barratt, Julian Barwell, John Baski, Rachel W. Bates, Joana Batista, Helen E. Baxendale, Gareth Baynam, David Bennett, Claire Bethune, Neha Bhatnagar, Shahnaz Bibi, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Marta Bleda
The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis
Sebastian Bode, Sandra Ammann, Waleed Al–Herz, Mihaela Bătăneanţ, Christopher C. Dvorak, Stephan Gehring, Andrew R. Gennery, Kimberly Gilmour, Luis Ignacio González‐Granado, U. Gross‐Wieltsch, Marianne Ifversen, Jenny Lingman Framme, Susanne Matthes‐Martin, Rolf M. Mesters, Isabelle Meyts, Joris M. van Montfrans, Jana Pachlopnik Schmid, Sung‐Yun Pai, Pere Soler‐Palacín, U. Schuermann, Volker Schuster, Markus G. Seidel, Carsten Speckmann, Polina Stepensky, Karl‐Walter Sykora, Bianca Tesi, Thomas Vraetz, C Waruiru, Yenan T. Bryceson, Despina Moshous, Kai Lehmberg, Michael B. Jordan, Stephan Ehl, for the Inborn Errors Working Party of the EBMT
Phenotypic and Genotypic Characterisation of Inflammatory Bowel Disease Presenting Before the Age of 2 years
Jochen Kammermeier, Robert Dziubak, Matilde Pescarin, Suzanne Drury, Heather Godwin, Kate Reeve, S. Chadokufa, B. Huggett, S Sider, Chela James, Nikki Acton, Elena Cernat, Marco Gasparetto, Gabi Noble-Jamieson, Fevronia Kiparissi, Mamoun Elawad, Phil Beales, Neil J. Sebire, Kimberly Gilmour, Holm H. Uhlig, Chiara Bacchelli, Neil Shah