User profiles for "author:U Radhakrishna"

Uppala Radhakrishna

- Verified email at unige.ch - Cited by 5234

Ujwal Radhakrishna

- Verified email at ti.com - Cited by 1414

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

…, M Lamacz, MG Thomas, C Gehrig, U Radhakrishna… - Nature …, 1998 - nature.com
Schizophrenia is a common disorder characterized by psychotic symptoms; diagnostic
criteria have been established 1. Family, twin and adoption studies suggest that both genetic …

Branchio‐oto‐renal syndrome (BOR): novel mutations in the EYA1 gene, and a review of the mutational genetics of BOR

…, SM Fischer, JL Sorensen, U Radhakrishna… - Human …, 2008 - Wiley Online Library
Branchio‐oto‐renal syndrome (BOR) is an autosomal dominant disorder characterized by
the association of branchial and external ear malformations, hearing loss, and renal …

[PDF][PDF] Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

…, H Ewald, TA Kruse, O Mors, U Radhakrishna… - The American Journal of …, 2003 - cell.com
Genome scans of bipolar disorder (BPD) have not produced consistent evidence for linkage.
The rank-based genome scan meta-analysis (GSMA) method was applied to 18 BPD …

Two-dimensional MoS2-enabled flexible rectenna for Wi-Fi-band wireless energy harvesting

X Zhang, J Grajal, JL Vazquez-Roy, U Radhakrishna… - Nature, 2019 - nature.com
The mechanical and electronic properties of two-dimensional materials make them
promising for use in flexible electronics 1, 2, 3. Their atomic thickness and large-scale …

Mutations in GJB6 cause hidrotic ectodermal dysplasia

…, J Zonana, S Antonarakis, U Radhakrishna… - Nature …, 2000 - nature.com
M. tuberculosis (Fig. 1). It seems that the detection of composite proteins is a complex
function of genome size, paralogy and phylogenetic distance. Almost one-half of the …

[PDF][PDF] Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1

…, JP Siffroi, S Christin-Maitre, U Radhakrishna… - The American Journal of …, 2010 - cell.com
One in seven couples worldwide are infertile, and male factor infertility accounts for
approximately 30%–50% of these cases. Although many genes are known to be essential …

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

…, S Minoshima, F Younus, SQ Mehdi, U Radhakrishna… - Nature …, 2001 - nature.com
Approximately 50% of childhood deafness is caused by mutations in specific genes.
Autosomal recessive loci account for approximately 80% of nonsyndromic genetic deafness …

[PDF][PDF] The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype …

U Radhakrishna, D Bornholdt, HS Scott… - The American Journal of …, 1999 - cell.com
Functional characterization of a gene often requires the discovery of the full spectrum of its
associated phenotypes. Mutations in the human GLI3 gene have been identified in Greig …

Design, Modeling, and Fabrication of Chemical Vapor Deposition Grown MoS2 Circuits with E-Mode FETs for Large-Area Electronics

L Yu, D El-Damak, U Radhakrishna, X Ling… - Nano …, 2016 - ACS Publications
Two-dimensional electronics based on single-layer (SL) MoS2 offers significant advantages
for realizing large-scale flexible systems owing to its ultrathin nature, good transport …

Negative capacitance behavior in a leaky ferroelectric

AI Khan, U Radhakrishna, K Chatterjee… - … on Electron Devices, 2016 - ieeexplore.ieee.org
We present a simulation study of the negative capacitance effect incorporating leakage
through the ferroelectric (FE) negative capacitor. The dynamics of the FE is modeled using …