Richard Crook - Publications, H-index & Citations

Richard Crook

Department of Neuroscience

52H指数

129论文数

1.2W被引数

收录论文 42

发表时间

Expanding the spectrum of annexin A11 proteinopathy in frontotemporal lobar degeneration and motor neuron disease 扩展前颞叶萎缩和运动神经元病中annexin A11蛋白病的谱系

Acta Neuropathologica

IF9.3

2025-11-12

OAAI

Nikhil B. Ghayal; Richard J. Crook; Angita Jain; Gunveen Sachdeva; Peizhou Jiang; Shanu F. Roemer; Hiroaki Sekiya; Michael A. DeTure; Matthew C. Baker; Wouter De Coster; Björn Oskarsson; Keith A. Josephs; Rosa Rademakers; Marka M. van Blitterswijk; Dennis W. Dickson

ABO-incompatible heart transplants in children aged 2-9 years: a new paradigm in transplant?ABO不合的心脏移植在2-9岁儿童中的应用：这是移植领域的新范式吗？

heart and lung transplantation

IF0

2025-08-20

PREAI

Paolo Hollis; Richard Issitt; Sebastiano A.G. Lava; Craig Laurence; Jacob Simmonds; Matthew Fenton; Nagarajan Muthialu; Alex Robertson; Richard Crook; Lori West; Michael Burch

Abundant transcriptomic alterations in the human cerebellum of patients with a C9orf72 repeat expansion

ACTA NEUROPATHOLOGICA

IF9.3

2024-04-19

OAAI

Udine, Evan; DeJesus-Hernandez, Mariely; Tian, Shulan; das Neves, Sofia Pereira; Crook, Richard; Finch, NiCole A.; Baker, Matthew C.; Pottier, Cyril; Graff-Radford, Neill R.; Boeve, Bradley F.; Petersen, Ronald C.; Knopman, David S.; Josephs, Keith A.; Oskarsson, Bjorn; Da Mesquita, Sandro; Petrucelli, Leonard; Gendron, Tania F.; Dickson, Dennis W.; Rademakers, Rosa; van Blitterswijk, Marka

Intraoperative anti-A/B immunoadsorption is associated with significantly reduced blood product utilization with similar outcomes in pediatric ABO-incompatible heart transplantation

JOURNAL OF HEART AND LUNG TRANSPLANTATION

IF6

2021-11-01

OAAI

Issitt, Richard; Booth, John; Crook, Richard; Robertson, Alex; Molyneux, Victoria; Richardson, Rebecca; Cross, Nigel; Shaw, Michael; Tsang, Victor; Muthurangu, Vivek; Sebire, Neil J.; Burch, Michael; Fenton, Matthew

A novel method for ABO-incompatible heart transplantation

JOURNAL OF HEART AND LUNG TRANSPLANTATION

IF6

2018-04-01

OAAI

Robertson, Alex; Issitt, Richard; Crook, Richard; Gustafsson, Kenth; Eddaoudi, Ayad; Tsang, Victor; Burch, Michael

Pathogenicity of exonic indels in fused in sarcoma in amyotrophic lateral sclerosis 肌萎缩侧索硬化症中融合肉瘤中外显子indel的致病性

NEUROBIOLOGY OF AGING

IF3.5

2012-02-01

OAAI

Rutherford, Nicola J.; Finch, Nicole A.; DeJesus-Hernandez, Mariely; Crook, Richard J. P.; Lomen-Hoerth, Catherine; Wszolek, Zbigniew K.; Uitti, Ryan J.; Graff-Radford, Neill R.; Rademakers, Rosa

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers

NEUROLOGY

IF8.5

2011-02-01

213

OAAI

Finch, N.; Carrasquillo, M. M.; Baker, M.; Rutherford, N. J.; Coppola, G.; DeJesus-Hernandez, M.; Crook, R.; Hunter, T.; Ghidoni, R.; Benussi, L.; Crook, J.; Finger, E.; Hantanpaa, K. J.; Karydas, A. M.; Sengdy, P.; Gonzalez, J.; Seeley, W. W.; Johnson, N.; Beach, T. G.; Mesulam, M.; Forloni, G.; Kertesz, A.; Knopman, D. S.; Uitti, R.; White, C. L., III; Caselli, R.; Lippa, C.; Bigio, E. H.; Wszolek, Z. K.; Binetti, G.; Mackenzie, I. R.; Miller, B. L.; Boeve, B. F.; Younkin, S. G.; Dickson, D. W.; Petersen, R. C.; Graff-Radford, N. R.; Geschwind, D. H.; Rademakers, R.

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

IF7.5

2010-06-20

176

OAAI

Boxer, Adam L.; Mackenzie, Ian R.; Boeve, Bradley F.; Baker, Matthew; Seeley, William W.; Crook, Richard; Feldman, Howard; Hsiung, Ging-Yuek R.; Rutherford, Nicola; Laluz, Victor; Whitwell, Jennifer; Foti, Dean; McDade, Eric; Molano, Jennifer; Karydas, Anna; Wojtas, Aleksandra; Goldman, Jill; Mirsky, Jacob; Sengdy, Pheth; DeArmond, Stephen; Miller, Bruce L.; Rademakers, Rosa

Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP

NEUROBIOLOGY OF AGING

IF3.5

2010-05-01

186

OAAI

Guerreiro, Rita Joao; Baquero, Miguel; Blesa, Rafael; Boada, Merce; Bras, Jose Miguel; Bullido, Maria J.; Calado, Ana; Crook, Richard; Ferreira, Carla; Frank, Ana; Gomez-Isla, Teresa; Hernandez, Isabel; Lleo, Alberto; Machado, Alvaro; Martinez-Lage, Pablo; Masdeu, Jose; Molina-Porcel, Laura; Molinuevo, Jose L.; Pastor, Pau; Perez-Tur, Jordi; Relvas, Rute; Oliveira, Catarina Resende; Ribeiro, Maria Helena; Rogaeva, Ekaterina; Sa, Alfredo; Samaranch, Lluis; Sanchez-Valle, Raquel; Santana, Isabel; Tarraga, Lluis; Valdivieso, Fernando; Singleton, Andrew; Hardy, John; Clarimon, Jordi

De Novo Truncating FUS Gene Mutation as a Cause of Sporadic Amyotrophic Lateral Sclerosis 从头截断FUS基因突变是散发性肌萎缩性侧索硬化症的原因

HUMAN MUTATION

IF3.7

2010-03-15

151

OAAI

DeJesus-Hernandez, Mariely; Kocerha, Jannet; Finch, NiCole; Crook, Richard; Baker, Matt; Desaro, Pamela; Johnston, Amelia; Rutherford, Nicola; Wojtas, Aleksandra; Kennelly, Kathleen; Wszolek, Zbigniew K.; Graff-Radford, Neill; Boylan, Kevin; Rademakers, Rosa

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members 血浆颗粒蛋白前体水平可预测额颞叶痴呆患者和无症状家庭成员的颗粒蛋白前体突变状态

BRAIN

IF11.7

2009-01-21

326

OAAI

Finch, NiCole; Baker, Matt; Crook, Richard; Swanson, Katie; Kuntz, Karen; Surtees, Rebecca; Bisceglio, Gina; Rovelet-Lecrux, Anne; Boeve, Bradley; Petersen, Ronald C.; Dickson, Dennis W.; Younkin, Steven G.; Deramecourt, Vincent; Crook, Julia; Graff-Radford, Neill R.; Rademakers, Rosa

Novel Mutations in TARDBP(TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

PLOS GENETICS

IF3.7

2008-09-19

436

OAAI

Rutherford, Nicola J.; Zhang, Yong-Jie; Baker, Matt; Gass, Jennifer M.; Finch, NiCole A.; Xu, Ya-Fei; Stewart, Heather; Kelley, Brendan J.; Kuntz, Karen; Crook, Richard J. P.; Sreedharan, Jemeen; Vance, Caroline; Sorenson, Eric; Lippa, Carol; Bigio, Eileen H.; Geschwind, Daniel H.; Knopman, David S.; Mitsumoto, Hiroshi; Petersen, Ronald C.; Cashman, Neil R.; Hutton, Mike; Shaw, Christopher E.; Boylan, Kevin B.; Boeve, Bradley; Graff-Radford, Neill R.; Wszolek, Zbigniew K.; Caselli, Richard J.; Dickson, Dennis W.; Mackenzie, Ian R.; Petrucelli, Leonard; Rademakers, Rosa

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

HUMAN MOLECULAR GENETICS

IF3.2

2008-08-21

268

OAAI

Rademakers, Rosa; Eriksen, Jason L.; Baker, Matt; Robinson, Todd; Ahmed, Zeshan; Lincoln, Sarah J.; Finch, Nicole; Rutherford, Nicola J.; Crook, Richard J.; Josephs, Keith A.; Boeve, Bradley F.; Knopman, David S.; Petersen, Ronald C.; Parisi, Joseph E.; Caselli, Richard J.; Wszolek, Zbigniew K.; Uitti, Ryan J.; Feldman, Howard; Hutton, Michael L.; Mackenzie, Ian R.; Graff-Radford, Neill R.; Dickson, Dennis W.

Cardiopulmonary bypass for surgical correction of congenital heart disease in children with sickle cell disease: a case series

ANAESTHESIA

IF6.9

2008-05-09

OAAI

Harban, F. M. J.; Connor, P.; Crook, R.; Bingham, R.

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

NEW ENGLAND JOURNAL OF MEDICINE

IF78.5

2007-08-23

213

OAAI

Dunckley, Travis; Huentelman, Matthew J.; Craig, David W.; Pearson, John V.; Szelinger, Szabolcs; Joshipura, Keta; Halperin, Rebecca F.; Stamper, Chelsea; Jensen, Kendall R.; Letizia, David; Hesterlee, Sharon E.; Pestronk, Alan; Levine, Todd; Bertorini, Tulio; Graves, Michael C.; Mozaffar, Tahseen; Jackson, Carlayne E.; Bosch, Peter; McVey, April; Dick, Arthur; Barohn, Richard; Lomen-Hoerth, Catherine; Rosenfeld, Jeffrey; O'Connor, Daniel T.; Zhang, Kuixing; Crook, Richard; Ryberg, Henrik; Hutton, Michael; Katz, Jonathan; Simpson, Ericka P.; Mitsumoto, Hiroshi; Bowser, Robert; Miller, Robert G.; Appel, Stanley H.; Stephan, Dietrich A.

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2007-04-01

OAAI

Melquist, Stacey; Craig, David W.; Huentelman, Matthew J.; Crook, Richard; Pearson, John V.; Baker, Matt; Zismann, Victoria L.; Gass, Jennifer; Adamson, Jennifer; Szelinger, Szabolcs; Corneveaux, Jason; Cannon, Ashley; Coon, Keith D.; Lincoln, Sarah; Adler, Charles; Tuite, Paul; Calne, Donald B.; Bigio, Eileen H.; Uitti, Ryan J.; Wszolek, Zbigniew K.; Golbe, Lawrence I.; Caselli, Richard J.; Graff-Radford, Neill; Litvan, Irene; Farrer, Matthew J.; Dickson, Dennis W.; Hutton, Mike; Stephan, Dietrich A.

ApoE2 allele, Down's syndrome, and dementia

NEUROBIOLOGY OF ALZHEIMER'S DISEASE

IF0

2006-12-17

PREAI

Royston, MC; Mann, D; PickeringBrown, S; Owen, F; Perry, R; Ragbavan, R; KhinNu, C; Tyner, S; Day, K; Crook, R; Hardy, J; Roberts, GW

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

HUMAN MOLECULAR GENETICS

IF3.2

2006-09-01

513

OAAI

Gass, Jennifer; Cannon, Ashley; Mackenzie, Ian R.; Boeve, Bradley; Baker, Matt; Adamson, Jennifer; Crook, Richard; Melquist, Stacey; Kuntz, Karen; Petersen, Ron; Josephs, Keith; Pickering-Brown, Stuart M.; Graff-Radford, Neill; Uitti, Ryan; Dickson, Dennis; Wszolek, Zbigniew; Gonzalez, John; Beach, Thomas G.; Bigio, Eileen; Johnson, Nancy; Weintraub, Sandra; Mesulam, Marsel; White, Charles L., III; Woodruff, Bryan; Caselli, Richard; Hsiung, Ging-Yuek; Feldman, Howard; Knopman, Dave; Hutton, Mike; Rademakers, Rosa

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

HUMAN MOLECULAR GENETICS

IF3.2

2005-09-29

146

OAAI

Rademakers, R; Melquist, S; Cruts, M; Theuns, J; Del-Favero, J; Poorkaj, P; Baker, M; Sleegers, K; Crook, R; De Pooter, T; Kacem, SB; Adamson, J; Van den Bossche, D; Van den Broeck, M; Gass, J; Corsmit, E; De Rijk, P; Thomas, N; Engelborghs, S; Heckman, M; Litvan, I; Crook, J; De Deyn, PP; Dickson, D; Schellenberg, GD; Van Broeckhoven, C; Hutton, ML

Phosphodiesterase 4D and 5-lipoxygenase activating protein in ischemic stroke

ANNALS OF NEUROLOGY

IF7.7

2005-01-01

105

OAAI

Meschia, JF; Brott, TG; Brown, RD; Crook, R; Worrall, BB; Kissela, B; Brown, WM; Rich, SS; Case, LD; Evans, EW; Hague, S; Singleton, A; Hardy, J

研究方向