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Items: 1 to 50 of 57

1.

Artificial intelligence analysis of newborn leucocyte epigenomic markers for the prediction of autism.

Bahado-Singh RO, Vishweswaraiah S, Aydas B, Mishra NK, Yilmaz A, Guda C, Radhakrishna U.

Brain Res. 2019 Dec 1;1724:146457. doi: 10.1016/j.brainres.2019.146457. Epub 2019 Sep 12.

PMID:
31521637
2.

The imperative of clinical and molecular research on neonatal opioid withdrawal syndrome.

Metpally RP, Krishnamurthy S, Moran KM, Weller AE, Crist RC, Reiner BC, Doyle GA, Ferraro TN, Radhakrishna U, Bahado-Singh R, Troiani V, Berrettini WH.

Mol Psychiatry. 2019 Sep 10. doi: 10.1038/s41380-019-0522-1. [Epub ahead of print] No abstract available.

PMID:
31506603
3.

Deep Learning/Artificial Intelligence and Blood-Based DNA Epigenomic Prediction of Cerebral Palsy.

Bahado-Singh RO, Vishweswaraiah S, Aydas B, Mishra NK, Guda C, Radhakrishna U.

Int J Mol Sci. 2019 Apr 27;20(9). pii: E2075. doi: 10.3390/ijms20092075.

4.

Placental DNA methylation changes for the detection of tetralogy of Fallot.

Bahado-Singh R, Vishweswaraiah S, Mishra NK, Guda C, Radhakrishna U.

Ultrasound Obstet Gynecol. 2019 Apr 12. doi: 10.1002/uog.20292. [Epub ahead of print]

PMID:
30977211
5.

Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD).

Radhakrishna U, Albayrak S, Zafra R, Baraa A, Vishweswaraiah S, Veerappa AM, Mahishi D, Saiyed N, Mishra NK, Guda C, Ali-Fehmi R, Bahado-Singh RO.

PLoS One. 2019 Mar 21;14(3):e0200229. doi: 10.1371/journal.pone.0200229. eCollection 2019.

6.

Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia.

Vishweswaraiah S, Swierkowska J, Ratnamala U, Mishra NK, Guda C, Chettiar SS, Johar KR, Mrugacz M, Karolak JA, Gajecka M, Radhakrishna U.

Sci Rep. 2019 Mar 11;9(1):4145. doi: 10.1038/s41598-019-40299-x.

7.

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

Zhang X, Grajal J, Vazquez-Roy JL, Radhakrishna U, Wang X, Chern W, Zhou L, Lin Y, Shen PC, Ji X, Ling X, Zubair A, Zhang Y, Wang H, Dubey M, Kong J, Dresselhaus M, Palacios T.

Nature. 2019 Feb;566(7744):368-372. doi: 10.1038/s41586-019-0892-1. Epub 2019 Jan 28.

PMID:
30692651
8.

A new species of Microhyla Tschudi, 1838 (Anura: Microhylidae) from West Coast of India: an integrative taxonomic approach.

Vineeth KK, Radhakrishna UK, Godwin RD, Anwesha S, Rajashekhar KP, Aravind NA.

Zootaxa. 2018 May 16;4420(2):151-179. doi: 10.11646/zootaxa.4420.2.1.

PMID:
30313540
9.

Newborn blood DNA epigenetic variations and signaling pathway genes associated with Tetralogy of Fallot (TOF).

Radhakrishna U, Vishweswaraiah S, Veerappa AM, Zafra R, Albayrak S, Sitharam PH, Saiyed NM, Mishra NK, Guda C, Bahado-Singh R.

PLoS One. 2018 Sep 13;13(9):e0203893. doi: 10.1371/journal.pone.0203893. eCollection 2018.

10.

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

Yu L, El-Damak D, Radhakrishna U, Ling X, Zubair A, Lin Y, Zhang Y, Chuang MH, Lee YH, Antoniadis D, Kong J, Chandrakasan A, Palacios T.

Nano Lett. 2016 Oct 12;16(10):6349-6356. Epub 2016 Sep 28.

PMID:
27633942
11.

Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS).

Radhakrishna U, Albayrak S, Alpay-Savasan Z, Zeb A, Turkoglu O, Sobolewski P, Bahado-Singh RO.

PLoS One. 2016 May 6;11(5):e0154010. doi: 10.1371/journal.pone.0154010. eCollection 2016.

12.

Expanding the spectrum of γ-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata.

Ratnamala U, Jhala D, Jain NK, Saiyed NM, Raveendrababu M, Rao MV, Mehta TY, Al-Ali FM, Raval K, Nair S, Chandramohan NK, Kuracha MR, Nath SK, Radhakrishna U.

Exp Dermatol. 2016 Apr;25(4):314-6. doi: 10.1111/exd.12911. Epub 2016 Feb 11. No abstract available. Erratum in: Exp Dermatol. 2017 May;26(5):467-468.

PMID:
26663538
13.

Epigenetic markers for newborn congenital heart defect (CHD).

Bahado-Singh RO, Zaffra R, Albayarak S, Chelliah A, Bolinjkar R, Turkoglu O, Radhakrishna U.

J Matern Fetal Neonatal Med. 2016;29(12):1881-7. doi: 10.3109/14767058.2015.1069811. Epub 2015 Oct 1.

PMID:
26429603
14.

Small players with a big role: MicroRNAs in pathophysiology of cleft lip and palate.

Radhakrishna U.

Indian J Hum Genet. 2012 Sep;18(3):272-3. doi: 10.4103/0971-6866.107973. No abstract available.

15.

Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.

Radhakrishna U, Nath SK, McElreavey K, Ratnamala U, Sun C, Maiti AK, Gagnebin M, Béna F, Newkirk HL, Sharp AJ, Everman DB, Murray JC, Schwartz CE, Antonarakis SE, Butler MG.

J Med Genet. 2012 Apr;49(4):270-6. doi: 10.1136/jmedgenet-2012-100826.

16.

Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmus.

Radhakrishna U, Ratnamala U, Deutsch S, Bartoloni L, Kuracha MR, Singh R, Banwait J, Bastola DK, Johar K, Nath SK, Antonarakis SE.

Eur J Hum Genet. 2012 Oct;20(10):1032-6. doi: 10.1038/ejhg.2012.60. Epub 2012 Apr 11.

17.

Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.

Klopocki E, Lohan S, Doelken SC, Stricker S, Ockeloen CW, Soares Thiele de Aguiar R, Lezirovitz K, Mingroni Netto RC, Jamsheer A, Shah H, Kurth I, Habenicht R, Warman M, Devriendt K, Kordass U, Hempel M, Rajab A, Mäkitie O, Naveed M, Radhakrishna U, Antonarakis SE, Horn D, Mundlos S.

J Med Genet. 2012 Feb;49(2):119-25. doi: 10.1136/jmedgenet-2011-100409. Epub 2011 Dec 6.

PMID:
22147889
18.

Identification of novel suggestive loci for high-grade myopia in Polish families.

Rydzanicz M, Nath SK, Sun C, Podfigurna-Musielak M, Frajdenberg A, Mrugacz M, Winters D, Ratnamala U, Radhakrishna U, Bejjani BA, Gajecka M.

Mol Vis. 2011;17:2028-39. Epub 2011 Jul 22.

19.

Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.

Ratnamala U, Lyle R, Rawal R, Singh R, Vishnupriya S, Himabindu P, Rao V, Aggarwal S, Paluru P, Bartoloni L, Young TL, Paoloni-Giacobino A, Morris MA, Nath SK, Antonarakis SE, Radhakrishna U.

Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6814-9. doi: 10.1167/iovs.10-6815. Erratum in: Invest Ophthalmol Vis Sci. 2011 Oct;52(11):7909.

20.

Clinical implications of novel activating EGFR mutations in malignant peritoneal mesothelioma.

Foster JM, Radhakrishna U, Govindarajan V, Carreau JH, Gatalica Z, Sharma P, Nath SK, Loggie BW.

World J Surg Oncol. 2010 Oct 13;8:88. doi: 10.1186/1477-7819-8-88.

21.

Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.

Bashamboo A, Ferraz-de-Souza B, Lourenço D, Lin L, Sebire NJ, Montjean D, Bignon-Topalovic J, Mandelbaum J, Siffroi JP, Christin-Maitre S, Radhakrishna U, Rouba H, Ravel C, Seeler J, Achermann JC, McElreavey K.

Am J Hum Genet. 2010 Oct 8;87(4):505-12. doi: 10.1016/j.ajhg.2010.09.009. Erratum in: Am J Hum Genet. 2010 Nov 12;87(5):736.

22.

Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region.

Al-Ali FM, Ratnamala U, Mehta TY, Naveed M, Al-Ali MT, Al-Khaja N, Sheth JJ, Master DC, Maiti AK, Chetan GK, Nath SK, Radhakrishna U.

Exp Dermatol. 2010 Sep;19(9):851-3. doi: 10.1111/j.1600-0625.2010.01088.x.

PMID:
20698881
23.

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

Gajecka M, Radhakrishna U, Winters D, Nath SK, Rydzanicz M, Ratnamala U, Ewing K, Molinari A, Pitarque JA, Lee K, Leal SM, Bejjani BA.

Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1531-9. doi: 10.1167/iovs.08-2173. Epub 2008 Nov 14.

24.

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

Orten DJ, Fischer SM, Sorensen JL, Radhakrishna U, Cremers CW, Marres HA, Van Camp G, Welch KO, Smith RJ, Kimberling WJ.

Hum Mutat. 2008 Apr;29(4):537-44. doi: 10.1002/humu.20691.

PMID:
18220287
25.

Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.

Beiraghi S, Nath SK, Gaines M, Mandhyan DD, Hutchings D, Ratnamala U, McElreavey K, Bartoloni L, Antonarakis GS, Antonarakis SE, Radhakrishna U.

Am J Hum Genet. 2007 Jul;81(1):180-8. Epub 2007 May 18.

26.

Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome.

Mehenni H, Resta N, Guanti G, Mota-Vieira L, Lerner A, Peyman M, Chong KA, Aissa L, Ince A, Cosme A, Costanza MC, Rossier C, Radhakrishna U, Burt RW, Picard D.

Dig Dis Sci. 2007 Aug;52(8):1924-33. Epub 2007 Apr 3.

PMID:
17404884
27.

Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.

Naveed M, Nath SK, Gaines M, Al-Ali MT, Al-Khaja N, Hutchings D, Golla J, Deutsch S, Bottani A, Antonarakis SE, Ratnamala U, Radhakrishna U.

Am J Hum Genet. 2007 Jan;80(1):105-11. Epub 2006 Nov 29.

28.

Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.

Radhakrishna U, Ratnamala U, Gaines M, Beiraghi S, Hutchings D, Golla J, Husain SA, Gambhir PS, Sheth JJ, Sheth FJ, Chetan GK, Naveed M, Solanki JV, Patel UC, Master DC, Memon R, Antonarakis GS, Antonarakis SE, Nath SK.

Am J Hum Genet. 2006 Sep;79(3):580-5. Epub 2006 Jul 21.

29.

Haplotypes, mutations and male fertility: the story of the testis-specific ubiquitin protease USP26.

Ravel C, El Houate B, Chantot S, Lourenço D, Dumaine A, Rouba H, Bandyopadahyay A, Radhakrishna U, Das B, Sengupta S, Mandelbaum J, Siffroi JP, McElreavey K.

Mol Hum Reprod. 2006 Oct;12(10):643-6. Epub 2006 Aug 3.

PMID:
16888075
30.

Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.

Lyle R, Radhakrishna U, Blouin JL, Gagos S, Everman DB, Gehrig C, Delozier-Blanchet C, Solanki JV, Patel UC, Nath SK, Gurrieri F, Neri G, Schwartz CE, Antonarakis SE.

Am J Med Genet A. 2006 Jul 1;140(13):1384-95.

PMID:
16691619
31.

Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis.

Naveed M, Al-Ali MT, Murthy SK, Al-Hajali S, Al-Khaja N, Deutsch S, Bottani A, Antonarakis SE, Nath SK, Radhakrishna U.

Am J Med Genet A. 2006 Jul 1;140(13):1440-6.

PMID:
16688753
32.

A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.

de Mollerat XJ, Gurrieri F, Morgan CT, Sangiorgi E, Everman DB, Gaspari P, Amiel J, Bamshad MJ, Lyle R, Blouin JL, Allanson JE, Le Marec B, Wilson M, Braverman NE, Radhakrishna U, Delozier-Blanchet C, Abbott A, Elghouzzi V, Antonarakis S, Stevenson RE, Munnich A, Neri G, Schwartz CE.

Hum Mol Genet. 2003 Aug 15;12(16):1959-71.

PMID:
12913067
33.

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI Jr, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lönnqvist J, Nöthen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Barden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N.

Am J Hum Genet. 2003 Jul;73(1):49-62. Epub 2003 Jun 11.

34.

Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome.

Driess S, Freese K, Bornholdt D, Kobelt A, Kress W, Mortier G, Radhakrishna U, Antonarakis SE, Rauch A, Suri M, Verheij JB, Woerle H, Grzeschik KH, Kalff-Suske M.

Hum Genet. 2003 Jan;112(1):103. No abstract available.

PMID:
12575660
35.
36.

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness.

Ben-Yosef T, Wattenhofer M, Riazuddin S, Ahmed ZM, Scott HS, Kudoh J, Shibuya K, Antonarakis SE, Bonne-Tamir B, Radhakrishna U, Naz S, Ahmed Z, Riazuddin S, Pandya A, Nance WE, Wilcox ER, Friedman TB, Morell RJ.

J Med Genet. 2001 Jun;38(6):396-400. No abstract available.

37.

An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree.

Radhakrishna U, Senol S, Herken H, Gucuyener K, Gehrig C, Blouin JL, Akarsu NA, Antonarakis SE.

Eur J Hum Genet. 2001 Jan;9(1):39-44.

38.

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

Scott HS, Kudoh J, Wattenhofer M, Shibuya K, Berry A, Chrast R, Guipponi M, Wang J, Kawasaki K, Asakawa S, Minoshima S, Younus F, Mehdi SQ, Radhakrishna U, Papasavvas MP, Gehrig C, Rossier C, Korostishevsky M, Gal A, Shimizu N, Bonne-Tamir B, Antonarakis SE.

Nat Genet. 2001 Jan;27(1):59-63.

PMID:
11137999
39.

Y-chromosome lineages trace diffusion of people and languages in southwestern Asia.

Quintana-Murci L, Krausz C, Zerjal T, Sayar SH, Hammer MF, Mehdi SQ, Ayub Q, Qamar R, Mohyuddin A, Radhakrishna U, Jobling MA, Tyler-Smith C, McElreavey K.

Am J Hum Genet. 2001 Feb;68(2):537-42. Epub 2000 Dec 27.

40.

Mutations in GJB6 cause hidrotic ectodermal dysplasia.

Lamartine J, Munhoz Essenfelder G, Kibar Z, Lanneluc I, Callouet E, Laoudj D, Lemaître G, Hand C, Hayflick SJ, Zonana J, Antonarakis S, Radhakrishna U, Kelsell DP, Christianson AL, Pitaval A, Der Kaloustian V, Fraser C, Blanchet-Bardon C, Rouleau GA, Waksman G.

Nat Genet. 2000 Oct;26(2):142-4. No abstract available.

PMID:
11017065
41.

Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.

Kibar Z, Dubé MP, Powell J, McCuaïg C, Hayflick SJ, Zonana J, Hovnanian A, Radhakrishna U, Antonarakis SE, Benohanian A, Sheeran AD, Stephan ML, Gosselin R, Kelsell DP, Christianson AL, Fraser FC, Der Kaloustian VM, Rouleau GA.

Eur J Hum Genet. 2000 May;8(5):372-80.

42.

Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity.

Blouin JL, Meeks M, Radhakrishna U, Sainsbury A, Gehring C, Saïl GD, Bartoloni L, Dombi V, O'Rawe A, Walne A, Chung E, Afzelius BA, Armengot M, Jorissen M, Schidlow DV, van Maldergem L, Walt H, Gardiner RM, Probst D, Guerne PA, Delozier-Blanchet CD, Antonarakis SE.

Eur J Hum Genet. 2000 Feb;8(2):109-18.

43.

The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.

Radhakrishna U, Bornholdt D, Scott HS, Patel UC, Rossier C, Engel H, Bottani A, Chandal D, Blouin JL, Solanki JV, Grzeschik KH, Antonarakis SE.

Am J Hum Genet. 1999 Sep;65(3):645-55.

44.

Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.

Antonarakis SE, Blouin JL, Lasseter VK, Gehrig C, Radhakrishna U, Nestadt G, Housman DE, Kazazian HH, Kalman K, Gutman G, Fantino E, Chandy KG, Gargus JJ, Pulver AE.

Am J Med Genet. 1999 Aug 20;88(4):348-51.

PMID:
10402501
45.

No evidence for linkage between schizophrenia and markers at chromosome 15q13-14.

Curtis L, Blouin JL, Radhakrishna U, Gehrig C, Lasseter VK, Wolyniec P, Nestadt G, Dombroski B, Kazazian HH, Pulver AE, Housman D, Bertrand D, Antonarakis SE.

Am J Med Genet. 1999 Apr 16;88(2):109-12.

PMID:
10206225
46.

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.

Blouin JL, Dombroski BA, Nath SK, Lasseter VK, Wolyniec PS, Nestadt G, Thornquist M, Ullrich G, McGrath J, Kasch L, Lamacz M, Thomas MG, Gehrig C, Radhakrishna U, Snyder SE, Balk KG, Neufeld K, Swartz KL, DeMarchi N, Papadimitriou GN, Dikeos DG, Stefanis CN, Chakravarti A, Childs B, Housman DE, Kazazian HH, Antonarakis S, Pulver AE.

Nat Genet. 1998 Sep;20(1):70-3.

PMID:
9731535
47.

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

Mehenni H, Blouin JL, Radhakrishna U, Bhardwaj SS, Bhardwaj K, Dixit VB, Richards KF, Bermejo-Fenoll A, Leal AS, Raval RC, Antonarakis SE.

Am J Hum Genet. 1997 Dec;61(6):1327-34.

48.

Mutation in GLI3 in postaxial polydactyly type A.

Radhakrishna U, Wild A, Grzeschik KH, Antonarakis SE.

Nat Genet. 1997 Nov;17(3):269-71. No abstract available.

PMID:
9354785
49.

The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region.

Radhakrishna U, Blouin JL, Mehenni H, Mehta TY, Sheth FJ, Sheth JJ, Solanki JV, Antonarakis SE.

Am J Med Genet. 1997 Jul 11;71(1):80-6.

PMID:
9215774
50.

Mapping one form of autosomal dominant postaxial polydactyly type A to chromosome 7p15-q11.23 by linkage analysis.

Radhakrishna U, Blouin JL, Mehenni H, Patel UC, Patel MN, Solanki JV, Antonarakis SE.

Am J Hum Genet. 1997 Mar;60(3):597-604.

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