John K. Fink - Publications, H-index & Citations

John K. Fink

University of Michigan

54H指数

185论文数

9.0K被引数

收录论文 41

发表时间

Toward therapeutic trials in primary lateral sclerosis 关于原发性侧索硬化症治疗试验的研究

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

IF2.8

2025-07-06

OAAI

Erica Scirocco; Matti D. Allen; Elisa Giacomelli; Senda Ajroud-Driss; Jinsy Andrews; Sandra Banack; Peter Bede; Michael Benatar; Ken Cheung; Philippe Corcia; Mamede de Carvalho; Lauren Elman; John K. Fink; Angela Genge; Orla Hardiman; Matthew Harms; Daragh Heitzman; Grace Jang; Osamu Kano; Matthew C. Kiernan; Ikjae Lee; Albert Ludolph; Paul Mehta; Hande Ozdinler; Kourosh Rezania; Paride Schito; Alexander V. Sherman; Vincenzo Silani; Eric Sorenson; Martin R. Turner; Leonard Van Den Berg; Hiroshi Mitsumoto; Sabrina Paganoni

The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN)痉挛性截瘫-卓越研究网络中心 (sp-cern)

NEUROLOGY-GENETICS

IF3.7

2025-04-01

PREAI

Schierbaum, Luca; Quiroz, Vicente; Yang, Kathryn; Rong, Joshua; Battaglia, Nicole; Zubair, Umar; Christie, Michelle; Davis, Marie; Calame, Daniel; Danzi, Matt C.; Finkel, Richard S.; Burns, Joshua; Gilbert, Donald L.; Mingbunjerdsuk, Dararat; Pruitt, Greg; Pruitt, Norma; Cobb, John; Sadjadi, Reza; Cashman, Christopher R.; Blackstone, Craig; Fink, John K.; Shy, Michael E.; Zuchner, Stephan; Ebrahimi-Fakhari, Darius

Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST 由SPAST的从头变异引起的早发性和严重的复杂遗传性痉挛性截瘫

MOVEMENT DISORDERS

IF7.6

2022-09-14

OAAI

Mo, Alisa; Saffari, Afshin; Kellner, Melanie; Dobler-Neumann, Marion; Jordan, Catherine; Srivastava, Siddharth; Zhang, Bo; Sahin, Mustafa; Fink, John K.; Smith, Linsley; Posey, Jennifer E.; Alter, Katharine E.; Toro, Camilo; Blackstone, Craig; Soldatos, Ariane G.; Christie, Michelle; Schule, Rebecca; Ebrahimi-Fakhari, Darius

Impact considerations of post-production processes on cell and gene drug products

CYTOTHERAPY

IF3.2

2022-06-01

PREAI

Fink, John; Scott, Michael; Rieck, Sebastian; Jones, Robert; Parisse, Jean-Sebastian; Hagen, Heidi; Lipsitz, Yonatan; Oh, Steve; Clarke, Dominic

Primary lateral sclerosis: consensus diagnostic criteria

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

IF7.5

2020-02-06

133

OAAI

Turner, Martin R.; Barohn, Richard J.; Corcia, Philippe; Fink, John K.; Harms, Matthew B.; Kiernan, Matthew C.; Ravits, John; Silani, Vincenzo; Simmons, Zachary; Statland, Jeffrey; van den Berg, Leonard H.; Mitsumoto, Hiroshi

THE EFFECT OF CRYOMEDIA SELECTION AND TRANSIENT WARMING EVENTS ON POST-CRYOPRESERVATION HUMAN MSC FUNCTION

CYTOTHERAPY

IF3.2

2018-05-01

PREAI

Hawkins, B. J.; Abazari, A.; Lock, L.; Ahsan, T.; Rowley, J. A.; Fink, J.; Mathew, A.

A roadmap for cost-of-goods planning to guide economic production of cell therapy products

CYTOTHERAPY

IF3.2

2017-12-01

OAAI

Lipsitz, Yonatan Y.; Milligan, William D.; Fitzpatrick, Ian; Stalmeijer, Evelien; Farid, Suzanne S.; Tan, Kah Yong; Smith, David; Perry, Robert; Carmen, Jessica; Chen, Allen; Mooney, Charles; Fink, John

BIOT™ CRYOPOD CARRIER: STANDARDIZED CRYOGENIC TEMPERATURE HANDLING OF CELLULAR THERAPIES

CYTOTHERAPY

IF3.2

2015-06-01

PREAI

Kunkel, E. J.; Comiso, S.; Fink, J.; Thompson, M.; Ehrhardt, R.

THERMAL EXCURSIONS OF CRYOGENICALLY FROZEN SINGLE VIALS BELOW-150°C) AND THE RISK OF RISING ABOVE TG: ANALYZING WARM-UP RATES FROM CRYOGENIC STORAGE TO BOTH DRY ICE AND AMBIENT TEMPERATURE ENVIRONMENTS

CYTOTHERAPY

IF3.2

2015-06-01

PREAI

Salvetti, M.; Fink, J.; Bartlett, A.; Stira, M.

PROTECTION OF INNOCENTS: CONTINUED SAMPLE WARM UP AFTER RETURN TO A CRYOGENIC ENVIRONMENT (BELOW-150°C) FOLLOWING A TRANSIENT AMBIENT PICKING OPERATION

CYTOTHERAPY

IF3.2

2015-06-01

PREAI

Zandi, B.; Warhurst, J.; Fink, J.

Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes

JOURNAL OF MEDICAL GENETICS

IF3.7

2014-12-05

OAAI

Hufnagel, Robert B.; Arno, Gavin; Hein, Nichole D.; Hersheson, Joshua; Prasad, Megana; Anderson, Yvonne; Krueger, Laura A.; Gregory, Louise C.; Stoetzel, Corinne; Jaworek, Thomas J.; Hull, Sarah; Li, Abi; Plagnol, Vincent; Willen, Christi M.; Morgan, Thomas M.; Prows, Cynthia A.; Hegde, Rashmi S.; Riazuddin, Saima; Grabowski, Gregory A.; Richardson, Rudy J.; Dieterich, Klaus; Huang, Taosheng; Revesz, Tamas; Martinez-Barbera, J. P.; Sisk, Robert A.; Jefferies, Craig; Houlden, Henry; Dattani, Mehul T.; Fink, John K.; Dollfus, Helene; Moore, Anthony T.; Ahmed, Zubair M.

The Alu-Rich Genomic Architecture of SPAST Predisposes to Diverse and Functionally Distinct Disease-Associated CNV Alleles

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2014-08-01

OAAI

Boone, Philip M.; Yuan, Bo; Campbell, Ian M.; Scul, Jennifer C.; Withers, Marjorie A.; Baggett, Brett C.; Beck, Christine R.; Shaw, Christine J.; Stankiewicz, Pawel; Moretti, Paolo; Goodwin, Wendy E.; Hein, Nichole; Fink, John K.; Seong, Moon-Woo; Seo, Soo Hyun; Park, Sung Sup; Karbassi, Izabela D.; Batish, Sat Dev; Ordonez-Ugalde, Andres; Quintans, Beatriz; Sobrido, Maria-Jesus; Stemmler, Susanne; Lupski, James R.

Morphea and Parry-Romberg syndrome associated with a mixed movement disorder

PARKINSONISM & RELATED DISORDERS

IF3.4

2013-12-01

OAAI

Walker, Ruth H.; Fink, John K.

Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12

HUMAN MUTATION

IF3.7

2013-08-12

OAAI

Landoure, Guida; Zhu, Peng-Peng; Lourenco, Charles M.; Johnson, Janel O.; Toro, Camilo; Bricceno, Katherine V.; Rinaldi, Carlo; Meilleur, Katherine G.; Sangare, Modibo; Diallo, Oumarou; Pierson, Tyler M.; Ishiura, Hiroyuki; Tsuji, Shoji; Hein, Nichole; Fink, John K.; Stoll, Marion; Nicholson, Garth; Gonzalez, Michael A.; Speziani, Fiorella; Duerr, Alexandra; Stevanin, Giovanni; Biesecker, Leslie G.; Accardi, John; Landis, Dennis M. D.; Gahl, William A.; Traynor, Bryan J.; Marques, Wilson, Jr.; Zuechner, Stephan; Blackstone, Craig; Fischbeck, Kenneth H.; Burnett, Barrington G.

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms

ACTA NEUROPATHOLOGICA

IF9.3

2013-07-30

383

OAAI

Fink, John K.

Whole-Genome Sequencing for Optimized Patient Management

SCIENCE TRANSLATIONAL MEDICINE

IF14.6

2011-06-15

228

OAAI

Bainbridge, Matthew N.; Wiszniewski, Wojciech; Murdock, David R.; Friedman, Jennifer; Gonzaga-Jauregui, Claudia; Newsham, Irene; Reid, Jeffrey G.; Fink, John K.; Morgan, Margaret B.; Gingras, Marie-Claude; Muzny, Donna M.; Hoang, Linh D.; Yousaf, Shahed; Lupski, James R.; Gibbs, Richard A.

Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zinc

NEUROTOXICOLOGY

IF3.9

2009-11-01

PREAI

Hedera, Peter; Peltier, Amanda; Fink, John K.; Wilcock, Sandy; London, Zachary; Brewer, George J.

Treatment of Wilson's disease with tetrathiomolybdate: V. control of free copper by tetrathiomolybdate and a comparison with trientine

TRANSLATIONAL RESEARCH

IF5.9

2009-08-01

134

PREAI

Brewer, George J.; Askari, Fred; Dick, Robert B.; Sitterly, Julia; Fink, John K.; Carlson, Martha; Kluin, Karen J.; Lorincz, Matthew T.

Sporadically occurring neurologic disease HSP genes and apparently sporadic spastic paraplegia

NEUROLOGY

IF8.5

2008-11-04

PREAI

Fink, John K.

Neuropathy target esterase gene mutations cause motor neuron disease

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2008-03-01

209

OAAI

Rainier, Shirley; Bui, Melanie; Mark, Erin; Thornas, Donald; Tokarz, Debra; Ming, Lei; Delaney, Colin; Richardson, Rudy J.; Albers, James W.; Matsunami, Nori; Stevens, Jeff; Coon, Hilary; Leppert, Mark; Fink, John K.

研究方向