Mohamad A. Mikati

Also affiliated with Duke University Hospital

MedicineNeuroscienceBiochemistry, 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 16 papers. Top paper: “De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis”.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.008

N/A

1.2DataRank · unranked

27 citations

Amar J. Majmundar, Kamal Khan, Tze Yin Lim, Shirlee Shril, Gina Jin +62 more

Antiseizure Medication Withdrawal in Seizure-Free Patients: Practice Advisory Update Summary

Neurology(2021)10.1212/wnl.0000000000012944

N/A

0.675DataRank · unranked

89 citations

Kimberly Pargeon, Alison Pack, Jay Varma, Jacqueline A. French, Benjamin Tolchin +4 more

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

Genetics in Medicine(2020)10.1038/s41436-020-01020-w

N/A

0.581DataRank · unranked

47 citations

Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker +53 more

The microRNA processorDROSHAis a candidate gene for a severe progressive neurological disorder

Human Molecular Genetics(2022)10.1093/hmg/ddac085

N/A

0.434DataRank · unranked

17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0.241DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations

Brain(2022)10.1093/brain/awac117

N/A

0DataRank · unranked

78 citations

Meethila Gade, Edward Yang, Hyun Yong Koh, Jinfeng Lü, Nicole M Walley +20 more

Early Clinical Variables Associated With Refractory Convulsive Status Epilepticus in Children

Neurology(2023)10.1212/wnl.0000000000207472

N/A

0DataRank · unranked

7 citations

Ravindra Arya, Tracy A. Glauser, Nicholas S. Abend, Cristina Barcia Aguilar, Marta Amengual‐Gual +68 more

Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene

European Journal of Human Genetics(2023)10.1038/s41431-023-01489-4

N/A

0DataRank · unranked

8 citations

Francesco Danilo Tiziano, Mohamad A. Mikati, Lisanne S. Vijfhuizen, Sophie Nicole, Gaëtan Lesca +19 more

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations

UNC Libraries(2024)10.17615/98hm-r135

N/A

0DataRank · unranked

0 citations

Peter Canoll, Anne F. Buckley, Gretchen K. Von Allmen, Hyun Yong Koh, Gerald A. Grant +20 more

Progressive central cardiorespiratory rate downregulation and intensifying epilepsy lead to sudden unexpected death in epilepsy in mouse model of the most common human ATP1A3 mutation

Epilepsia(2025)10.1111/epi.18236

N/A

0DataRank · unranked

8 citations

Amitesh Verma, Minu‐Tshyeto Bidzimou, Debolina D. Biswas, Emily Da Cruz, M. Srour +6 more

Epileptic encephalopathy with features of rapid‐onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation

Epileptic Disorders(2020)10.1684/epd.2020.1127

N/A

0DataRank · unranked

9 citations

Jason Richards, Marie McDonald, Allyn McConkie‐Rosell, Nicholas Stong, Joan Jasien +3 more

Variation in Neurodegeneration‐Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida

Annals of the Child Neurology Society(2025)10.1002/cns3.70016

N/A

0DataRank · unranked

0 citations

Jacques Stout, Mohamad A. Mikati, Robert J. Anderson, Brittany Nave, Herbert E. Fuchs +4 more

Cognitive and motor function in adults with spina bifida myelomeningocele: a pilot study

IAS(2020)10.1007/s00381-020-04964-1

N/A

0DataRank · unranked

5 citations

Mohamad A. Mikati, Michaela Kolářová, Brian N. Smith, Stephanie Thera, Pierre Lee +1 more

Factors associated with long‐term outcomes in pediatric refractory status epilepticus

Epilepsia(2021)10.1111/epi.16984

N/A

0DataRank · unranked

30 citations

Cristina Barcia Aguilar, Juan Piantino, Kevin Chapman, Iván Sánchez Fernández, Marta Amengual‐Gual +37 more

Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations

Epilepsy & Behavior(2021)10.1016/j.yebeh.2020.107732

N/A

0DataRank · unranked

28 citations

David M. Mueller, Milton Pratt, Melanie Bonner, Courtney Elliott, Arsen Hunanyan +9 more

Somatic mutation involving diverse genes leads to a spectrum of focal cortical malformations

medRxiv(2021)10.1101/2021.12.22.21267563

N/A

0DataRank · unranked

4 citations

Meethila Gade, Edward Yang, Hyun Yong Koh, Nicole M. Walley, Anne F. Buckley +18 more