ScholarIQanswers from OpenAlex & ORCID
Nigel Williams
ResearcherPublications, citations & collaboration network
Nigel Williams is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Nigel Williams have?
ScholarIQindexed works
Nigel Williams has 629 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Nigel Williams have?
ScholarIQcitation count
Nigel Williams has 42,262 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Nigel Williams?
ScholarIQh-index
Nigel Williams has an h-index of 87 in OpenAlex.
What is the i10-index of Nigel Williams?
ScholarIQi10-index
Nigel Williams has an i10-index of 244 in OpenAlex.
What is the ORCID of Nigel Williams?
ScholarIQorcid
The ORCID for Nigel Williams is on the source record.
What is the OpenAlex record for Nigel Williams?
ScholarIQopenalex
The OpenAlex for Nigel Williams is on the source record.
What are the most-cited papers on Nigel Williams?
ScholarIQmost cited works
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson, J. Raphael Gibbs, Jennifer C. Schymick, Hannu Laaksovirta, John C. van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M. Remes, Alice Kaganovich, Sonja W. Scholz, Jamie Duckworth, Jinhui Ding, Daniel W. Harmer, Dena G. Hernandez, Janel O. Johnson, Kin Y. Mok, Mina Ryten, Daniah Trabzuni, Rita Guerreiro, Richard W. Orrell, James Neal, Alex Murray, Justin Pearson, Iris E. Jansen, David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chiò, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Elisa Majounie, Alan E. Renton, Kin Y. Mok, Elise G.P. Dopper, Adrian J. Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simón‐Sánchez, John C. van Swieten, Yevgeniya Abramzon, Janel O. Johnson, Michael Sendtner, Roger Pamphlett, Richard W. Orrell, Simon Mead, Katie Sidle, Henry Houlden, Jonathan D. Rohrer, Karen Morrison, Hardev Pall, Kevin Talbot, Olaf Ansorge, Dena G. Hernandez, Sampath Arepalli, Mario Sabatelli, Gabriele Mora, Massimo Corbo, Fabio Giannini, Andrea Calvo, Elisabet Englund, Giuseppe Borghero, Gianluca Floris, Anne M. Remes, Hannu Laaksovirta, Leo McCluskey, John Q. Trojanowski, Vivianna M. Van Deerlin, Gerard D. Schellenberg, Michael A. Nalls, Vivian E. Drory, Chin‐Song Lu, Tu‐Hsueh Yeh, Hiroyuki Ishiura, Yuji Takahashi, Shoji Tsuji, Isabelle Le Ber, Alexis Brice, Carsten Drepper, Nigel Williams, Janine Kirby, Pamela J. Shaw, John Hardy, Pentti J. Tienari, Peter Heutink, Huw R. Morris, Stuart Pickering‐Brown, Bryan J. Traynor
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
Nigel Williams, Irina Zaharieva, Andrew Martin, K. Langley, Kiran K. Mantripragada, Ragnheiður Fossdal, Hreinn Stefánsson, Kari Stefansson, Páll Magnússon, Ólafur Ó. Guðmundsson, Ómar Gústafsson, Peter Holmans, Michael J. Owen, Michael O‘Donovan, Anita Thapar
Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder
Benjamin M. Neale, Sarah E. Medland, Stephan Ripke, Philip Asherson, Barbara Franke, Klaus‐Peter Lesch, Stephen V. Faraone, Thuy Trang Nguyen, H. Schäfer, Peter Holmans, Mark J. Daly, Hans‐Christoph Steinhausen, Christine M. Freitag, Andreas Reif, Tobias Renner, Marcel Romanos, Jasmin Romanos, Susanne Walitza, Andreas Warnke, Jobst Meyer, Haukur Pálmason, Jan K. Buitelaar, Alejandro Arias Vásquez, Nanda Lambregts-Rommelse, Michael Gill, Richard Anney, Kate Langely, Michael O‘Donovan, Nigel Williams, Michael J. Owen, Anita Thapar, Lindsey Kent, Joseph A. Sergeant, Herbert Roeyers, Eric Mick, Joseph Biederman, Alysa E. Doyle, Susan L. Smalley, Sandra K. Loo, Håkon Håkonarson, Josephine Elia, Alexandre A. Todorov, Ana Miranda, Fernando Mulas, Richard P. Ebstein, Aribert Rothenberger, Tobias Banaschewski, Robert D. Oades, Edmund Sonuga‐Barke, James J. McGough, Laura Nisenbaum, Frank A. Middleton, Xiaolan Hu, Stan F. Nelson
Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
Nigel Williams, Barbara Franke, Eric Mick, Richard Anney, Christine M. Freitag, Michael Gill, Anita Thapar, Michael O‘Donovan, Michael J. Owen, Peter Holmans, Lindsey Kent, Frank A. Middleton, Yanli Zhang‐James, Lu Liu, Jobst Meyer, Thuy Trang Nguyen, Jasmin Romanos, Marcel Romanos, Christiane Seitz, Tobias Renner, Susanne Walitza, Andreas Warnke, Haukur Pálmason, Jan K. Buitelaar, Nanda Rommelse, Alejandro Arias Vásquez, Ziarih Hawi, K. Langley, Joseph A. Sergeant, Hans‐Christoph Steinhausen, Herbert Roeyers, Joseph Biederman, Irina Zaharieva, Håkon Håkonarson, Josephine Elia, Anath C. Lionel, Jennifer Crosbie, Christian R. Marshall, Russell Schachar, Stephen W. Scherer, Alexandre A. Todorov, Susan L. Smalley, Sandra K. Loo, Stanley F. Nelson, Corina Shtir, Philip Asherson, Andreas Reif, Klaus‐Peter Lesch, Stephen V. Faraone