ScholarIQanswers from OpenAlex & ORCID
Thomas D. Bird
ResearcherPublications, citations & collaboration network
Thomas D. Bird is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Thomas D. Bird have?
ScholarIQindexed works
Thomas D. Bird has 454 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Thomas D. Bird have?
ScholarIQcitation count
Thomas D. Bird has 48,492 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Thomas D. Bird?
ScholarIQh-index
Thomas D. Bird has an h-index of 89 in OpenAlex.
What is the i10-index of Thomas D. Bird?
ScholarIQi10-index
Thomas D. Bird has an i10-index of 216 in OpenAlex.
What is the OpenAlex record for Thomas D. Bird?
ScholarIQopenalex
The OpenAlex for Thomas D. Bird is on the source record.
What are the most-cited papers on Thomas D. Bird?
ScholarIQmost cited works
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
D.R. Rosen, Teepu Siddique, David T. Patterson, Denise A. Figlewicz, Peter C. Sapp, Afif Hentati, Deirdre Donaldson, Jun Goto, J. O'Regan, Han‐Xiang Deng, Zohra Rahmani, Aldis Krizus, Diane McKenna‐Yasek, Annarueber Cayabyab, Sandra M. Gaston, Ralph Berger, Rudolph E. Tanzi, John Halperin, Brian Herzfeldt, R. van den Bergh, W.‐Y. Hung, Thomas D. Bird, Gang Deng, Donald W. Mulder, Celestine Smyth, Nigel G. Laing, Edwin Soriano, Margaret A. Pericak‐Vance, Jonathan Haines, Guy A. Rouleau, James S. Gusella, H. Robert Horvitz, Robert Brown
Secreted amyloid β–protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease
Donalyn Scheuner, Christopher B. Eckman, M. Jensen, X.H. Song, Martin Citron, Nobuhiro Suzuki, Thomas D. Bird, John Hardy, M. Hutton, Walter A. Kukull, Eric B. Larson, Ephrat Levy‐Lahad, Matti Viitanen, Elaine R. Peskind, Parvoneh Poorkaj, Gerald D. Schellenberg, Rudolph E. Tanzi, Wilma Wasco, Lars Lannfelt, Dennis J. Selkoe, Samuel Younkin
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
Ephrat Levy‐Lahad, Wilma Wasco, Parvoneh Poorkaj, Donna Romano, Junko Oshima, Warren H. Pettingell, Chang-En Yu, P. D. Jondro, Stephen D. Schmidt, Kai Wang, Annette C. Crowley, Ying‐Hui Fu, Suzanne Y. Guénette, David J. Galas, Ellen Nemens, Ellen M. Wijsman, Thomas D. Bird, Gerard D. Schellenberg, Rudolph E. Tanzi
Mutations in SEPT9 cause hereditary neuralgic amyotrophy
Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis, Anja Schirmacher, Nathalie Verpoorten, Jan Meuleman, Giles D. Watts, Els De Vriendt, Peter Young, Florian Stögbauer, Hartmut Halfter, Joy Irobi, D. Goossens, Jurgen Del‐Favero, Benjamin G Betz, Hyun Hor, G. Kurlemann, Thomas D. Bird, Eila Airaksinen, Tarja Mononen, Adolfo Pou Serradell, J M Prats, Christine Van Broeckhoven, Peter De Jonghe, Vincent Timmerman, E B Ringelstein, Phillip F. Chance