Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 22

1.

GlyStruct: glycation prediction using structural properties of amino acid residues.

Reddy HM, Sharma A, Dehzangi A, Shigemizu D, Chandra AA, Tsunoda T.

BMC Bioinformatics. 2019 Feb 4;19(Suppl 13):547. doi: 10.1186/s12859-018-2547-x.

2.

Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites.

Bruels CC, Li C, Mendoza T, Khan J, Reddy HM, Estrella EA, Ghosh PS, Darras BT, Lidov HGW, Pacak CA, Kunkel LM, Modave F, Draper I, Kang PB.

Mol Genet Genomic Med. 2019 Mar;7(3):e552. doi: 10.1002/mgg3.552. Epub 2019 Jan 28.

3.

Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan.

Saha M, Reddy HM, Salih MA, Estrella E, Jones MD, Mitsuhashi S, Cho KA, Suzuki-Hatano S, Rizzo SA, Hamad MH, Mukhtar MM, Hamed AA, Elseed MA, Lek M, Valkanas E, MacArthur DG, Kunkel LM, Pacak CA, Draper I, Kang PB.

Physiol Genomics. 2018 Nov 1;50(11):929-939. doi: 10.1152/physiolgenomics.00036.2018. Epub 2018 Aug 31.

PMID:
30345904
4.

Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions.

Saha M, Mitsuhashi S, Jones MD, Manko K, Reddy HM, Bruels CC, Cho KA, Pacak CA, Draper I, Kang PB.

Hum Mol Genet. 2017 Aug 1;26(15):2984-3000. doi: 10.1093/hmg/ddx189.

5.

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.

Cummings BB, Marshall JL, Tukiainen T, Lek M, Donkervoort S, Foley AR, Bolduc V, Waddell LB, Sandaradura SA, O'Grady GL, Estrella E, Reddy HM, Zhao F, Weisburd B, Karczewski KJ, O'Donnell-Luria AH, Birnbaum D, Sarkozy A, Hu Y, Gonorazky H, Claeys K, Joshi H, Bournazos A, Oates EC, Ghaoui R, Davis MR, Laing NG, Topf A; Genotype-Tissue Expression Consortium, Kang PB, Beggs AH, North KN, Straub V, Dowling JJ, Muntoni F, Clarke NF, Cooper ST, Bönnemann CG, MacArthur DG.

Sci Transl Med. 2017 Apr 19;9(386). pii: eaal5209. doi: 10.1126/scitranslmed.aal5209.

6.

A Pooled Sequencing Approach Identifies a Candidate Meiotic Driver in Drosophila.

Wei KH, Reddy HM, Rathnam C, Lee J, Lin D, Ji S, Mason JM, Clark AG, Barbash DA.

Genetics. 2017 May;206(1):451-465. doi: 10.1534/genetics.116.197335. Epub 2017 Mar 3.

7.

The sensitivity of exome sequencing in identifying pathogenic mutations for LGMD in the United States.

Reddy HM, Cho KA, Lek M, Estrella E, Valkanas E, Jones MD, Mitsuhashi S, Darras BT, Amato AA, Lidov HG, Brownstein CA, Margulies DM, Yu TW, Salih MA, Kunkel LM, MacArthur DG, Kang PB.

J Hum Genet. 2017 Feb;62(2):243-252. doi: 10.1038/jhg.2016.116. Epub 2016 Oct 6.

8.

Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt.

Reddy HM, Hamed SA, Lek M, Mitsuhashi S, Estrella E, Jones MD, Mahoney LJ, Duncan AR, Cho KA, Macarthur DG, Kunkel LM, Kang PB.

Muscle Nerve. 2016 Oct;54(4):690-5. doi: 10.1002/mus.25094. Epub 2016 Aug 24.

9.

Protein interactions on telomeric retrotransposons in Drosophila.

Takács S, Biessmann H, Reddy HM, Mason JM, Török T.

Int J Biol Sci. 2012;8(7):1055-61. doi: 10.7150/ijbs.4460. Epub 2012 Aug 15.

10.

BRM-Parser: a tool for comprehensive analysis of BLAST and RepeatMasker results.

Bajpai A, Sridhar S, Reddy HM, Jesudasan RA.

In Silico Biol. 2007;7(4-5):399-403.

PMID:
18391232
11.
12.

Novel noncoding RNA from human Y distal heterochromatic block (Yq12) generates testis-specific chimeric CDC2L2.

Jehan Z, Vallinayagam S, Tiwari S, Pradhan S, Singh L, Suresh A, Reddy HM, Ahuja YR, Jesudasan RA.

Genome Res. 2007 Apr;17(4):433-40. Epub 2006 Nov 9.

13.

Neonatal and infant mortality in the ten years (1993 to 2003) of the Gadchiroli field trial: effect of home-based neonatal care.

Bang AT, Reddy HM, Deshmukh MD, Baitule SB, Bang RA.

J Perinatol. 2005 Mar;25 Suppl 1:S92-107.

PMID:
15791283
14.
15.

Low birth weight and preterm neonates: can they be managed at home by mother and a trained village health worker?

Bang AT, Baitule SB, Reddy HM, Deshmukh MD, Bang RA.

J Perinatol. 2005 Mar;25 Suppl 1:S72-81.

PMID:
15791281
16.

Is home-based diagnosis and treatment of neonatal sepsis feasible and effective? Seven years of intervention in the Gadchiroli field trial (1996 to 2003).

Bang AT, Bang RA, Stoll BJ, Baitule SB, Reddy HM, Deshmukh MD.

J Perinatol. 2005 Mar;25 Suppl 1:S62-71.

PMID:
15791280
17.

Reduced incidence of neonatal morbidities: effect of home-based neonatal care in rural Gadchiroli, India.

Bang AT, Bang RA, Reddy HM, Deshmukh MD, Baitule SB.

J Perinatol. 2005 Mar;25 Suppl 1:S51-61.

PMID:
15791279
19.
20.
21.

Methods and the baseline situation in the field trial of home-based neonatal care in Gadchiroli, India.

Bang AT, Bang RA, Reddy HM, Deshmukh MD.

J Perinatol. 2005 Mar;25 Suppl 1:S11-7.

PMID:
15791273
22.

Supplemental Content

Loading ...
Support Center