Milind C Mahajan
Overview
Explore the profile of Milind C Mahajan including associated specialties, affiliations and a list of published articles.
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18
Citations
1142
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Recent Articles
1.
Mahajan M, Mclellan A
Methods Mol Biol
. 2019 Oct;
2076:85-108.
PMID: 31586323
Next-generation sequencing (NGS) is transforming clinical research and diagnostics, vastly enhancing our ability to identify novel disease-causing genetic mutations and perform comprehensive diagnostic testing in the clinic. Whole-exome sequencing (WES)...
2.
Fromer M, Roussos P, Sieberts S, Johnson J, Kavanagh D, Perumal T, et al.
Nat Neurosci
. 2016 Sep;
19(11):1442-1453.
PMID: 27668389
Over 100 genetic loci harbor schizophrenia-associated variants, yet how these variants confer liability is uncertain. The CommonMind Consortium sequenced RNA from dorsolateral prefrontal cortex of people with schizophrenia (N =...
3.
Sanderson S, Linderman M, Kasarskis A, Bashir A, Diaz G, Mahajan M, et al.
Genome Med
. 2013 Dec;
5(12):113.
PMID: 24373383
Background: Multiple laboratories now offer clinical whole genome sequencing (WGS). We anticipate WGS becoming routinely used in research and clinical practice. Many institutions are exploring how best to educate geneticists...
4.
Fang G, Munera D, Friedman D, Mandlik A, Chao M, Banerjee O, et al.
Nat Biotechnol
. 2012 Nov;
30(12):1232-9.
PMID: 23138224
Single-molecule real-time (SMRT) DNA sequencing allows the systematic detection of chemical modifications such as methylation but has not previously been applied on a genome-wide scale. We used this approach to...
5.
Walker R, Schulz V, Tikhonova I, Mahajan M, Mane S, Arroyo Muniz M, et al.
Mov Disord
. 2011 Nov;
27(4):539-43.
PMID: 22038564
Neuroacanthocytoses are neurodegenerative disorders marked by phenotypic and genetic heterogeneity. There are several associated genetic loci, and many defects, including gene deletions and insertions, and missense, nonsense, and splicing mutations,...
6.
Wontakal S, Guo X, Will B, Shi M, Raha D, Mahajan M, et al.
PLoS Genet
. 2011 Jun;
7(6):e1001392.
PMID: 21695229
PU.1 is a hematopoietic transcription factor that is required for the development of myeloid and B cells. PU.1 is also expressed in erythroid progenitors, where it blocks erythroid differentiation by...
7.
Bordner K, Kitchen R, Carlyle B, George E, Mahajan M, Mane S, et al.
Exp Gerontol
. 2011 Apr;
46(8):643-59.
PMID: 21453768
Aging in humans is associated with parallel changes in cognition, motivation, and motoric performance. Based on the human aging literature, we hypothesized that this constellation of age-related changes is mediated...
8.
Karmakar S, Mahajan M, Schulz V, Boyapaty G, Weissman S
EMBO J
. 2010 Sep;
29(19):3260-71.
PMID: 20808282
DNA replication, repair, transcription and chromatin structure are intricately associated nuclear processes, but the molecular links between these events are often obscure. In this study, we have surveyed the protein...
9.
Yasukochi Y, Maruyama O, Mahajan M, Padden C, Euskirchen G, Schulz V, et al.
Proc Natl Acad Sci U S A
. 2010 Feb;
107(8):3704-9.
PMID: 20133578
The DNA methylation status of human X chromosomes from male and female neutrophils was identified by high-throughput sequencing of HpaII and MspI digested fragments. In the intergenic and intragenic regions...
10.
Steiner L, Maksimova Y, Schulz V, Wong C, Raha D, Mahajan M, et al.
Mol Cell Biol
. 2009 Aug;
29(20):5399-412.
PMID: 19687298
Erythrocyte membrane protein genes serve as excellent models of complex gene locus structure and function, but their study has been complicated by both their large size and their complexity. To...