Shane McKee

7.5k citations

44 papers · 1.1k indexed · h-index 17

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Pathology and Forensic Medicine top 10%
- Genetic factors in colorectal cancer

Papers in ⓘ

Microbiology 1
Genetics 21
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Eamonn R. Maher (2 shared papers)Frances M. Richards (1 shared paper)Janusz Jankowski (1 shared paper)D. Gareth Evans (1 shared paper)Trevor Cole (1 shared paper)M. Helen Rajpar (1 shared paper)C. McKeown (1 shared paper)D. S. A. Sanders (1 shared paper)
Journals: Clinical Genetics (6 papers)The American Journal of Human Genetics (3 papers)Orphanet Journal of Rare Diseases (2 papers)Genes (2 papers)European Journal of Human Genetics (1 paper)
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Shane McKee

43 papers receiving 1.1k citations

Peers

Countries citing papers authored by Shane McKee

Since Specialization

Citations

This map shows the geographic impact of Shane McKee's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Shane McKee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shane McKee more than expected).

Fields of papers citing papers by Shane McKee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Shane McKee. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Shane McKee. The network helps show where Shane McKee may publish in the future.

Co-authors

The 25 scholars most cited alongside Shane McKee, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Shane McKee Line = papers co-authored together Shane McKee links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Germline E-cadherin Gene (CDH1) Mutations Predispose to Familial Gastric Cancer and Colorectal Cancer Human Molecular Genetics ·Frances M. Richards, Shane McKee, M. Helen Rajpar, Trevor Cole, D. Gareth Evans, Janusz Jankowski, C. McKeown, D. S. A. Sanders, Eamonn R. Maher	1999	251
2	Mapping of Deletion and Translocation Breakpoints in 1q44 Implicates the Serine/Threonine Kinase AKT3 in Postnatal Microcephaly and Agenesis of the Corpus Callosum The American Journal of Human Genetics ·Elena Boland, Jill Clayton‐Smith, Victoria G. Woo, Shane McKee, Forbes Manson, Līvija Medne, Elaine H. Zackai, Eric A. Swanson, David Fitzpatrick, Kathleen J. Millen, Elliott H. Sherr, William B. Dobyns, Graeme C. Black	2007	117
3	Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2) Clinical Genetics ·Siddharth Banka, Damien Lederer, Valérie Benoît, Emma Jenkins, Emma Howard, Sancha Bunstone, Bronwyn Kerr, Shane McKee, I. Christopher Lloyd, D. Shears, Helen Stewart, Susan M. White, Ravi Savarirayan, Grazia M.S. Mancini, Diane Beysen, Ronald D. Cohn, Bernard Grisart, Isabelle Maystadt, Dian Donnai	2014	91
4	Clinical and genetic analysis of patients with pancreatic neuroendocrine tumors associated with von Hippel-Lindau disease Surgery ·Steven K. Libutti, Peter L. Choyke, H. Richard Alexander, G.M. Glenn, David L. Bartlett, Berton Zbar, Irina A. Lubensky, Shane McKee, Eamonn R. Maher, W. Marston Linehan, McClellan M. Walther	2000	87
5	De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability American Journal of Medical Genetics Part A ·Michael Parker, Alan Fryer, Deborah Shears, Katherine Lachlan, Shane McKee, Alex Magee, Shehla Mohammed, Pradeep Vasudevan, Soo‐Mi Park, Valérie Benoît, Damien Lederer, Isabelle Maystadt, DDD Study, David Fitzpatrick	2015	79
6	Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis Genes and Immunity ·E Aganna, Philip N. Hawkins, Seza Özen, Tom Pettersson, A Bybee, Shane McKee, Helen J. Lachmann, Leena Karenko, Annamari Ranki, Ayşı̇n Bakkaloğlu, Nesrin Beşbaş, Rezan Topaloğlu, Hal M. Hoffman, G. A. Hitman, Patricia Woo, Michael McDermott	2004	47
7	7q11.23 Microduplication: a recognizable phenotype Clinical Genetics ·Abhijit Dixit, Shane McKee, Sahar Mansour, SG Mehta, George A. Tanteles, Violetta Anastasiadou, PC Patsalis, Katherine Martin, Simon McCullough, Mohnish Suri, Ajoy Sarkar	2012	37
8	Software Practitioner Perspectives on Merge Conflicts and Resolutions Shane McKee, Nicholas Nelson, Anita Sarma, Danny Dig	2017	36
9	MLL2 mosaic mutations and intragenic deletion–duplications in patients with Kabuki syndrome Clinical Genetics ·Siddharth Banka, Emma Howard, Sancha Bunstone, KE Chandler, Briedgeen Kerr, Katherine Lachlan, Shane McKee, SG Mehta, A. C. Tavares, John Tolmie, Donnai Dian	2012	35
10	A scoping review and proposed workflow for multi-omic rare disease research Orphanet Journal of Rare Diseases ·Katie Kerr, Helen McAneney, Laura J. Smyth, Caitlin Bailie, Shane McKee, Amy Jayne McKnight	2020	32
11	A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies The American Journal of Human Genetics ·Kevin C. Nixon, Justine Rousseau, Max H. Stone, Mohammed Sarikahya, Sophie Ehresmann, Seiji Mizuno, Naomichi Matsumoto, Noriko Miyake, Diana Baralle, Shane McKee, Kosuke Izumi, Alyssa Ritter, Solveig Heide, Delphine Héron, Christel Depienne, Hannah Titheradge, Jamie M. Kramer, Philippe M. Campeau	2019	27
12	The life-cycle of merge conflicts: processes, barriers, and strategies Empirical Software Engineering ·Nicholas Nelson, Caius Brindescu, Shane McKee, Anita Sarma, Danny Dig	2019	27
13	The clinical presentation caused by truncating CHD8 variants Clinical Genetics ·Sofia Douzgou, Hui Liang, Kay Metcalfe, Suresh Somarathi, Marc Tischkowitz, Mohamed Wafik, Usha Kini, Shane McKee, Laura Yates, Marta Bertoli, Sally Ann Lynch, Susan Holder, (unknown), (unknown)	2019	26
14	De novo direct duplication 2 (p12 p21) with paternally inherited pericentric inversion 2p11.2 2q12.2 Clinical Genetics ·Alex Magee, Mervyn Humphreys, Shane McKee, Moira D. Stewart, N. C. Nevin	1998	24
15	Differential cytokine secretion results from p65 and c-Rel NF-κB subunit signaling in peripheral blood mononuclear cells of TNF receptor-associated periodic syndrome patients Cellular Immunology ·Belinda Nedjai, G. A. Hitman, Leigh D Church, Kirsten Minden, Margo L. Whiteford, Shane McKee, Susanna Stjernberg, Tom Pettersson, Annamari Ranki, Philip N. Hawkins, Peter D. Arkwright, Michael McDermott, Mark D. Turner	2011	20
16	Deletions in 14q24.1q24.3 are associated with congenital heart defects, brachydactyly, and mild intellectual disability American Journal of Medical Genetics Part A ·Barbara Oehl‐Jaschkowitz, Olivier Vanakker, Anne De Paepe, Björn Menten, Thomas G. Martin, Georg F. Weber, Alexander Christmann, Romain Krier, Simone Scheid, Susan McNerlan, Shane McKee, Andreas Tzschach	2013	17
17	A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome Clinical Genetics ·Richard O. Day, B Beckett, Dian Donnai, Alan Fryer, M. Heidenblad, Peter Howard, Bronwyn Kerr, Sahar Mansour, Una Maye, Shane McKee, Shehla Mohammed, Elizabeth Sweeney, May Tassabehji, BBA De Vries, Jill Clayton‐Smith	2008	17
18	Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency Orphanet Journal of Rare Diseases ·Joe C.H. Sim, Susan M. White, Elizabeth Fitzpatrick, Gabrielle R. Wilson, Greta Gillies, Kate Pope, Hayley S. Mountford, Pernille Mathiesen Tørring, Shane McKee, Anneke T. Vulto‐van Silfhout, Shalini N. Jhangiani, Donna M. Muzny, Richard J. Leventer, Martin B. Delatycki, David J. Amor, Paul J. Lockhart	2014	15
19	Shwachman-Diamond syndrome: a complex case demonstrating the potential for misdiagnosis as asphyxiating thoracic dystrophy (Jeune syndrome) BMC Pediatrics ·Steven J. Keogh, Shane McKee, Sarah Smithson, D. Grier, Colin G. Steward	2012	14
20	Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study Journal of Medical Genetics ·Ahmed Alhendi, Derek Lim, Shane McKee, Meriel McEntagart, Katriona Tatton-Brown, I. Karen Temple, Justin H. Davies, Deborah Mackay	2021	13

About Shane McKee

Shane McKee is a scholar working on Microbiology, Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health and Immunology, having authored 44 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (6 papers), Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromatin Remodeling and Cancer (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genetics, Bioinformatics, and Biomedical Research (3 papers) and Distributed and Parallel Computing Systems (3 papers). The work is most often cited by research in Genetics (467 citations), Pathology and Forensic Medicine (171 citations), Molecular Biology (561 citations), Cancer Research (112 citations) and Developmental Neuroscience (30 citations). Shane McKee has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Eamonn R. Maher, Frances M. Richards, Janusz Jankowski, D. Gareth Evans, Trevor Cole, M. Helen Rajpar, C. McKeown, D. S. A. Sanders, David Fitzpatrick and Anita Sarma. Their work appears in journals such as Clinical Genetics, The American Journal of Human Genetics, Orphanet Journal of Rare Diseases, Genes and European Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact