Gail E Herman
Overview
Explore the profile of Gail E Herman including associated specialties, affiliations and a list of published articles.
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Articles
47
Citations
2727
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Recent Articles
1.
Fu J, Satterstrom F, Peng M, Brand H, Collins R, Dong S, et al.
Nat Genet
. 2022 Aug;
54(9):1320-1331.
PMID: 35982160
Some individuals with autism spectrum disorder (ASD) carry functional mutations rarely observed in the general population. We explored the genes disrupted by these variants from joint analysis of protein-truncating variants...
2.
Arredondo K, Myers C, Hansen-Kiss E, Mathew M, Jayaraman V, Siemon A, et al.
J Child Neurol
. 2022 Apr;
37(6):517-523.
PMID: 35384780
Background And Purpose: Mutations in have classically been associated with benign familial neonatal and infantile seizures and more recently identified in patients with neurodevelopmental disorders and abnormal electroencephalogram (EEG) findings....
3.
Miller D, Lee K, Chung W, Gordon A, Herman G, Klein T, et al.
Genet Med
. 2021 Aug;
23(8):1582-1584.
PMID: 34345026
No abstract available.
4.
Miller D, Lee K, Gordon A, Amendola L, Adelman K, Bale S, et al.
Genet Med
. 2021 May;
23(8):1391-1398.
PMID: 34012069
No abstract available.
5.
Miller D, Lee K, Chung W, Gordon A, Herman G, Klein T, et al.
Genet Med
. 2021 May;
23(8):1381-1390.
PMID: 34012068
No abstract available.
6.
Repnikova E, Lyalin D, McDonald K, Astbury C, Hansen-Kiss E, Cooley L, et al.
Eur J Med Genet
. 2019 Mar;
63(1):103636.
PMID: 30836150
Copy number variations (CNVs) of the CNTN6 gene - a member of the contactin gene superfamily - have been previously proposed to have an association with neurodevelopmental and autism spectrum...
7.
Barrie E, Pinsonneault J, Sadee W, Hollway J, Handen B, Smith T, et al.
J Dev Phys Disabil
. 2018 Sep;
30(3):355-371.
PMID: 30197492
Background: Frequent non-pathogenic genetic variants may act as moderators of phenotypic severity for complex disorders such as autism spectrum disorder (ASD). We previously identified polymorphisms affecting mRNA expression of candidate...
8.
Islam M, Herman G, de Los Reyes E
Semin Pediatr Neurol
. 2018 Jul;
26:25-27.
PMID: 29961511
Recent technological advances in exome sequencing or targeted gene sequencing with epilepsy panels have allowed clinicians to better understand the pathogenesis and clinical presentation of children with epilepsy. We present...
9.
Kumar R, Gardner A, Homan C, Douglas E, Mefford H, Wieczorek D, et al.
Hum Mutat
. 2018 Jun;
39(8):1126-1138.
PMID: 29851191
Highly conserved TREX-mediated mRNA export is emerging as a key pathway in neuronal development and differentiation. TREX subunit variants cause neurodevelopmental disorders (NDDs) by interfering with mRNA export from the...
10.
Overholt K, Rose M, Joshi S, Herman G, Bajwa R, Abu-Arja R, et al.
Blood Adv
. 2018 Jan;
1(4):279-281.
PMID: 29296943
HCT prior to onset of neurologic symptoms in children with OSTM1 osteopetrosis does not halt neurologic progression.