Timothy Lotze

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 18 papers. Top paper: “A novel de novo intronic variant in ITPR1 causes Gillespie syndrome”.

A novel de novo intronic variant in ITPR1 causes Gillespie syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62232

N/A

0.434DataRank · unranked

17 citations

Ming‐Ming Jiang, Xiaohui Li, Ronit Marom, Hongzheng Dai, David R. Murdock +16 more

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum

Genetics in Medicine(2024)10.1016/j.gim.2024.101273

N/A

0.373DataRank · unranked

11 citations

Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano +62 more

GARS‐related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61544

N/A

0DataRank · unranked

28 citations

Rajarshi Ghosh, Molly E. Kuo, William Hong, Jaehyung Lim, Saunder Bernes +14 more

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00870-6

N/A

0DataRank · unranked

117 citations

Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo +95 more

Familial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis

Neurology Neuroimmunology & Neuroinflammation(2021)10.1212/nxi.0000000000001049

N/A

0DataRank · unranked

18 citations

T. Charles Casper, Soe Mar, Jayne Ness, Patricia Plumb, Shannon Liang +26 more

Rasch Analysis of the Pediatric Quality of Life Inventory 4.0 Generic Core Scales Administered to Patients With Duchenne Muscular Dystrophy

Value in Health(2021)10.1016/j.jval.2021.05.016

N/A

0DataRank · unranked

12 citations

Joel Iff, Erik Henricson, V. Vishwanathan, S. Chidambaranathan, W. Douglas Biggar +33 more

Biallelic Pathogenic Variants in TNNT3 Associated With Congenital Myopathy

Neurology Genetics(2021)10.1212/nxg.0000000000000589

N/A

0DataRank · unranked

16 citations

Jawid M. Fatih, Isabella Herman, Zeynep Coban‐Akdemir, Haowei Du, Shalini N. Jhangiani +9 more

Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variant

Annals of Clinical and Translational Neurology(2021)10.1002/acn3.51454

N/A

0DataRank · unranked

2 citations

Jawid M. Fatih, Isabella Herman, Zeynep Coban‐Akdemir, Haowei Du, Tadahiro Mitani +12 more

Therapeutic Response in Pediatric Neuromyelitis Optica Spectrum Disorder

Neurology(2022)10.1212/wnl.0000000000201625

N/A

0DataRank · unranked

13 citations

Michael Waltz, Gregory Aaen, Leslie Benson, Mark Gorman, Manu S. Goyal +18 more

The Texas Children's Hospital Experience With Pediatric Anti-NMDAR Encephalitis: 2010-2021

Neurology(2022)10.1212/01.wnl.0000903472.11556.dd

N/A

0DataRank · unranked

0 citations

Yike Jiang, Tim Erickson, Timothy Lotze, Eyal Muscal, Kristy O. Murray +1 more

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.006

N/A

0DataRank · unranked

37 citations

Tanya L. Schwab, Sarah K. Macklin‐Mantia, A. Reghan Foley, Filippo Pinto e Vairo, Davut Pehli̇van +25 more

Fulminant Anti-Myelin Oligodendrocyte Glycoprotein-Associated Cerebral Cortical Encephalitis: Case Series of a Severe Pediatric Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Phenotype

Pediatric Neurology(2023)10.1016/j.pediatrneurol.2023.07.002

N/A

0DataRank · unranked

22 citations

Alexander J. Sandweiss, Timothy A. Erickson, Jonathan M. Yarimi, Alexander Ankar, Victoria A. Hardwick +8 more

Cation leak through the ATP1A3 pump causes spasticity and intellectual disability

Brain(2023)10.1093/brain/awad124

N/A

0DataRank · unranked

13 citations

Cristina Moreno Vadillo, Seth Berger, Timothy Lotze, Marwan Shinawi, Javaher Poupak +24 more

Predictors of a relapsing course in myelin oligodendrocyte glycoprotein antibody-associated disease

Journal of Neurology Neurosurgery & Psychiatry(2024)10.1136/jnnp-2024-333464

N/A

0DataRank · unranked

27 citations

Vinícius Andreoli Schoeps, Jonathan Race, Michael Waltz, Siefaddeen Sharayah, Zahra Nasr +25 more

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

medRxiv(2024)10.1101/2024.02.09.24302464

N/A

0DataRank · unranked

2 citations

Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano +57 more

Acute flaccid myelitis: cause, diagnosis, and management

The Lancet(2020)10.1016/s0140-6736(20)32723-9

N/A

0DataRank · unranked

181 citations

Kevin Messacar, Lina Benson, Riley Bove, Jessica L. Carpenter, Thomas O. Crawford +95 more

Clinical characterization of Collagen XII‐related disease caused by biallelic COL12A1 variants

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.52225

N/A

0DataRank · unranked

3 citations

Dimah Saade, Pinki Munot, Chamindra G. Laverty, Hailey Pinz, Yaqun Zou +24 more

Improved relapse recovery in paediatric compared to adult multiple sclerosis

Brain(2020)10.1093/brain/awaa199

N/A

0DataRank · unranked

90 citations

Greg Aaen, Anita Belman, Leslie Benson, Mark Gorman, Manu S. Goyal +17 more