James C Mullikin
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Explore the profile of James C Mullikin including associated specialties, affiliations and a list of published articles.
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181
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28629
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Recent Articles
1.
Schnitzler C, Chang E, Waletich J, Quiroga-Artigas G, Wong W, Nguyen A, et al.
Genome Res
. 2024 Mar;
34(3):498-513.
PMID: 38508693
is a colonial marine hydroid that shows remarkable biological properties, including the capacity to regenerate its entire body throughout its lifetime, a process made possible by its adult migratory stem...
2.
Hansen N, Wang X, Tegegn M, Liu Z, Gouveia M, Hill G, et al.
bioRxiv
. 2023 Dec;
PMID: 38076833
In regions where reads don't align well to a reference, it is generally difficult to characterize structural variation using short read sequencing. Here, we utilize machine learning classifiers and short...
3.
Schnitzler C, Chang E, Waletich J, Quiroga-Artigas G, Wong W, Nguyen A, et al.
bioRxiv
. 2023 Oct;
PMID: 37786714
is a colonial marine hydroid that exhibits remarkable biological properties, including the capacity to regenerate its entire body throughout its lifetime, a process made possible by its adult migratory stem...
4.
Sok P, Sabo A, Almli L, Jenkins M, Nembhard W, Agopian A, et al.
Am J Med Genet A
. 2023 Mar;
191(6):1546-1556.
PMID: 36942736
The etiology of biliary atresia (BA) is unknown, but recent studies suggest a role for rare protein-altering variants (PAVs). Exome sequencing data from the National Birth Defects Prevention Study on...
5.
Huene A, Sanders S, Ma Z, Nguyen A, Koren S, Michaca M, et al.
Proc Natl Acad Sci U S A
. 2022 Sep;
119(40):e2207374119.
PMID: 36161920
Most colonial marine invertebrates are capable of allorecognition, the ability to distinguish between themselves and conspecifics. One long-standing question is whether invertebrate allorecognition genes are homologous to vertebrate histocompatibility genes....
6.
Li J, Yang W, Wang Y, Ma C, Curry C, McGoldrick D, et al.
Am J Med Genet A
. 2022 Jun;
188(8):2376-2388.
PMID: 35716026
Anophthalmia and microphthalmia (A/M) are rare birth defects affecting up to 2 per 10,000 live births. These conditions are manifested by the absence of an eye or reduced eye volumes...
7.
Nurk S, Koren S, Rhie A, Rautiainen M, Bzikadze A, Mikheenko A, et al.
Science
. 2022 Mar;
376(6588):44-53.
PMID: 35357919
Since its initial release in 2000, the human reference genome has covered only the euchromatic fraction of the genome, leaving important heterochromatic regions unfinished. Addressing the remaining 8% of the...
8.
Pitsava G, Feldkamp M, Pankratz N, Lane J, Kay D, Conway K, et al.
Birth Defects Res
. 2022 Mar;
114(7):215-227.
PMID: 35274497
Background: Sacral agenesis (SA) consists of partial or complete absence of the caudal end of the spine and often presents with additional birth defects. Several studies have examined gene variants...
9.
Rudd M, Hansen N, Zhang X, Urick M, Zhang S, Merino M, et al.
PLoS One
. 2022 Jan;
17(1):e0251286.
PMID: 35081118
Endometrioid endometrial carcinomas (EECs) are the most common histological subtype of uterine cancer. Late-stage disease is an adverse prognosticator for EEC. The purpose of this study was to analyze EEC...
10.
Zhou Y, Sood R, Wang Q, Carrington B, Park M, Young A, et al.
Epilepsia Open
. 2021 Mar;
6(1):102-111.
PMID: 33681653
Objective: Our goal was to perform detailed clinical and genomic analysis of a large multigenerational Chinese family with 21 individuals showing symptoms of Familial Cortical Myoclonic Tremor with Epilepsy (FCMTE)...