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L

Lyndal Henden

Walter Reed National Military Medical Center
H指数:13
被引数:717

个人简介

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教育背景

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工作经历

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荣誉奖项

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Identity-by-descent to resolve reduced penetrance and advance gene discovery in neurodegenerative disease

基于亲缘关系的分析以解决神经退行性疾病中的遗传力降低问题并推动基因发现

Brain
IF11.7
2026-09-250
OAAI
Lyndal Henden; Sandrine Chan Moi Fat; Andrew Smith; Isabel Li; Thomas J Nicholas; Miran Mrkela; Daniel O’Shaughnessy; Zoe Zussa; Natalie Grima; Emily P McCann; Jennifer A Fifita; Simon D Topp; Alfredo Iacoangeli; Dominic B Rowe; Garth A Nicholson; Carol Dobson-Stone; John B Kwok; Olivier Piguet; Glenda M Halliday; Claire Troakes; Ammar Al-Chalabi; Christopher E Shaw; Richard H Roxburgh; Matthew C Kiernan; Roger Pamphlett; Benoit Liquet; Allan F McRae; Tian Lin; Nigel G Laing; Merrilee Needham; David Schultz; Susan Mathers; Steve Vucic; Robert Henderson; Pamela McCombe; Anjali Henders; Aaron R Quinlan; Emma L Scotter; Bradley N Smith; Ian P Blair; Kelly L Williams
Characterising the motif composition and allele length distribution of ZFHX3 GGC repeat expansions in amyotrophic lateral sclerosis

鉴定肌萎缩侧索硬化症中ZFHX3 GGC串联重复扩展的基序组成和等位基因长度分布

Journal of Human Genetics
IF2.5
2026-09-150
OAAI
Zoe N. Zussa; Andrew N. Smith; Joke J.F.A van Vugt; Daniel S. O’Shaughnessy; Natalie Grima; Sandrine Chan Moi Fat; Ian P. Blair; Dominic B. Rowe; Roger Pamphlett; Garth A. Nicholson; Matthew C. Kiernan; Wouter van Rheenen; Jan Veldink; Kelly L. Williams; Lyndal Henden
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration (vol 13, 6901, 2022)

SOD1-mediated ALS表型显示症状发作年龄与疾病持续时间之间的脱钩 (第13卷，6901，2022)

NATURE COMMUNICATIONS
IF15.7
2024-07-020
OAAI
Opie-Martin, Sarah; Iacoangeli, Alfredo; Topp, Simon D.; Abel, Olubunmi; Mayl, Keith; Mehta, Puja R.; Shatunov, Aleksey; Fogh, Isabella; Bowles, Harry; Limbachiya, Naomi; Spargo, Thomas P.; Al-Khleifat, Ahmad; Williams, Kelly L.; Jockel-Balsarotti, Jennifer; Bali, Taha; Self, Wade; Henden, Lyndal; Nicholson, Garth A.; Ticozzi, Nicola; McKenna-Yasek, Diane; Tang, Lu; Shaw, Pamela J.; Chio, Adriano; Ludolph, Albert; Weishaupt, Jochen H.; Landers, John E.; Glass, Jonathan D.; Mora, Jesus S.; Robberecht, Wim; Van Damme, Philip; McLaughlin, Russell; Hardiman, Orla; van den Berg, Leonard; Veldink, Jan H.; Corcia, Phillippe; Stevic, Zorica; Siddique, Nailah; Silani, Vincenzo; Blair, Ian P.; Fan, Dong-sheng; Esselin, Florence; de la Cruz, Elisa; Camu, William; Basak, Nazli A.; Siddique, Teepu; Miller, Timothy; Brown, Robert H.; Al-Chalabi, Ammar; Shaw, Christopher E.
Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementia

肌萎缩侧索硬化和额颞叶痴呆中致病性UBQLN2的海马聚集特征

BRAIN
IF11.7
2024-05-043
OAAI
Thumbadoo, Kyrah M.; Dieriks, Birger, V; Murray, Helen C.; Swanson, Molly E., V; Yoo, Ji Hun; Mehrabi, Nasim F.; Turner, Clinton; Dragunow, Michael; Faull, Richard L. M.; Curtis, Maurice A.; Siddique, Teepu; Shaw, Christopher E.; Newell, Kathy L.; Henden, Lyndal; Williams, Kelly L.; Nicholson, Garth A.; Scotter, Emma L.
Short tandem repeat expansions in sporadic amyotrophic lateral sclerosis and frontotemporal dementia

散发性肌萎缩性侧索硬化症和额颞痴呆的短串联重复扩增

SCIENCE ADVANCES
IF12.5
2023-05-0515
OAAI
Henden, Lyndal; Fearnley, Liam G.; Grima, Natalie; McCann, Emily P.; Dobson-Stone, Carol; Fitzpatrick, Lauren; Friend, Kathryn; Hobson, Lynne; Fat, Sandrine Chan Moi; Rowe, Dominic B.; D'Silva, Susan; Kwok, John B.; Halliday, Glenda M.; Kiernan, Matthew C.; Mazumder, Srestha; Timmins, Hannah C.; Zoing, Margaret; Pamphlett, Roger; Adams, Lorel; Bahlo, Melanie; Blair, Ian P.; Williams, Kelly L.
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

SOD1-mediated ALS表型显示症状发作年龄与疾病持续时间之间的脱钩

NATURE COMMUNICATIONS
IF15.7
2022-11-1222
OAAI
Opie-Martin, Sarah; Iacoangeli, Alfredo; Topp, Simon D.; Abel, Olubunmi; Mayl, Keith; Mehta, Puja R.; Shatunov, Aleksey; Fogh, Isabella; Bowles, Harry; Limbachiya, Naomi; Spargo, Thomas P.; Al-Khleifat, Ahmad; Williams, Kelly L.; Jockel-Balsarotti, Jennifer; Bali, Taha; Self, Wade; Henden, Lyndal; Nicholson, Garth A.; Ticozzi, Nicola; McKenna-Yasek, Diane; Tang, Lu; Shaw, Pamela J.; Chio, Adriano; Ludolph, Albert; Weishaupt, Jochen H.; Landers, John E.; Glass, Jonathan D.; Mora, Jesus S.; Robberecht, Wim; Van Damme, Philip; McLaughlin, Russell; Hardiman, Orla; van den Berg, Leonard; Veldink, Jan H.; Corcia, Phillippe; Stevic, Zorica; Siddique, Nailah; Silani, Vincenzo; Blair, Ian P.; Fan, Dong-sheng; Esselin, Florence; de la Cruz, Elisa; Camu, William; Basak, Nazli A.; Siddique, Teepu; Miller, Timothy; Brown, Robert H.; Al-Chalabi, Ammar; Shaw, Christopher E.
Splicing factor proline and glutamine rich intron retention, reduced expression and aggregate formation are pathological features of amyotrophic lateral sclerosis

剪接因子脯氨酸和谷氨酰胺丰富的内含子保留，表达减少和聚集体形成是肌萎缩侧索硬化的病理特征

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
IF3.4
2021-08-0211
OAAI
Hogan, Alison L.; Grima, Natalie; Fifita, Jennifer A.; McCann, Emily P.; Heng, Benjamin; Fat, Sandrine Chan Moi; Wu, Sharlynn; Maharjan, Ram; Cain, Amy K.; Henden, Lyndal; Rayner, Stephanie; Tarr, Ingrid; Zhang, Katharine Y.; Zhao, Qiongyi; Zhang, Zong-Hong; Wright, Amanda; Lee, Albert; Morsch, Marco; Yang, Shu; Williams, Kelly L.; Blair, Ian P.
Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
IF7.5
2019-11-0512
PREAI
McCann, Emily P.; Fifita, Jennifer A.; Grima, Natalie; Galper, Jasmin; Mehta, Prachi; Freckleton, Sarah E.; Zhang, Katharine Y.; Henden, Lyndal; Hogan, Alison L.; Chan Moi Fat, Sandrine; Wu, Sharlynn S. L.; Jagaraj, Cyril J.; Berning, Britt A.; Williams, Kelly Louise; Twine, Natalie A.; Bauer, Denis; Piguet, Olivier; Hodges, John; Kwok, John B. J.; Halliday, Glenda M.; Kiernan, Matthew C.; Atkin, Julie; Rowe, Dominic B.; Nicholson, Garth A.; Walker, Adam K.; Blair, Ian P.; Yang, Shu
EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO
HUMAN MUTATION
IF3.7
2017-01-2361
OA
Skopkova, Martina; Hennig, Friederike; Shin, Byung-Sik; Turner, Clesson E.; Stanikova, Daniela; Brennerova, Katarina; Stanik, Juraj; Fischer, Ute; Henden, Lyndal; Mueller, Ulrich; Steinberger, Daniela; Leshinsky-Silver, Esther; Bottani, Armand; Kurdiova, Timea; Ukropec, Jozef; Nyitrayova, Olga; Kolnikova, Miriam; Klimes, Iwar; Borck, Guntram; Bahlo, Melanie; Haas, Stefan A.; Kim, Joo-Ran; Lotspeich-Cole, Leda E.; Gasperikova, Daniela; Dever, Thomas E.; Kalscheuer, Vera M.
Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2-2q11.2
HUMAN GENETICS
IF3.6
2016-07-0127
PREAI
Henden, Lyndal; Freytag, Saskia; Afawi, Zaid; Baldassari, Sara; Berkovic, Samuel F.; Bisulli, Francesca; Canafoglia, Laura; Casari, Giorgio; Crompton, Douglas Ewan; Depienne, Christel; Gecz, Jozef; Guerrini, Renzo; Helbig, Ingo; Hirsch, Edouard; Keren, Boris; Klein, Karl Martin; Labauge, Pierre; LeGuern, Eric; Licchetta, Laura; Mei, Davide; Nava, Caroline; Pippucci, Tommaso; Rudolf, Gabrielle; Scheffer, Ingrid Eileen; Striano, Pasquale; Tinuper, Paolo; Zara, Federico; Corbett, Mark; Bahlo, Melanie

研究方向

暂未获取到该数据
K
Kelly L. Williams
H 指数:39论文数:143被引数:1.2万
I
Ian P. Blair
H 指数:51论文数:196被引数:1.5万
N
Natalie Grima
H 指数:24论文数:74被引数:2,172
E
Emily P. McCann
H 指数:19论文数:47被引数:2,353
D
Dominic B. Rowe
H 指数:40论文数:152被引数:7,421
S
Sandrine Chan Moi Fat
H 指数:8论文数:18被引数:338
G
Garth A. Nicholson
H 指数:80论文数:410被引数:2.6万
J
Jennifer A. Fifita
H 指数:27论文数:53被引数:5,271
M
Matthew C. Kiernan
H 指数:107论文数:1,108被引数:4.4万
M
Melanie Bahlo
H 指数:76论文数:479被引数:2.1万