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Items: 1 to 50 of 73

1.

Detection of Secondary Metabolites as Biomarkers for the Early Diagnosis and Prevention of Type 2 Diabetes.

Al-Aama JY, Al Mahdi HB, Salama MA, Bakur KH, Alhozali A, Mosli HH, Bahijri SM, Bahieldin A, Willmitzer L, Edris S.

Diabetes Metab Syndr Obes. 2019 Dec 17;12:2675-2684. doi: 10.2147/DMSO.S215528. eCollection 2019.

2.

Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects.

Gaboon NEA, Banaganapalli B, Nasser K, Razeeth M, Alsaedi MS, Rashidi OM, Abdelwehab LS, Alahmadi TS, Safdar OY, Shaik J, Choudhry HMZ, Al-Numan HH, Khan MI, Al-Aama JY, Elango R, Shaik NA.

Saudi J Biol Sci. 2020 Jan;27(1):324-334. doi: 10.1016/j.sjbs.2019.10.001. Epub 2019 Oct 18.

3.

Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients.

Kamal NM, Sahly AN, Banaganapalli B, Rashidi OM, Shetty PJ, Al-Aama JY, Shaik NA, Elango R, Saadah OI.

Saudi J Biol Sci. 2020 Jan;27(1):271-278. doi: 10.1016/j.sjbs.2019.09.006. Epub 2019 Sep 11.

4.

Genetic Mosaicism in Calmodulinopathy.

Wren LM, Jiménez-Jáimez J, Al-Ghamdi S, Al-Aama JY, Bdeir A, Al-Hassnan ZN, Kuan JL, Foo RY, Potet F, Johnson CN, Aziz MC, Carvill GL, Kaski JP, Crotti L, Perin F, Monserrat L, Burridge PW, Schwartz PJ, Chazin WJ, Bhuiyan ZA, George AL Jr.

Circ Genom Precis Med. 2019 Sep;12(9):375-385. doi: 10.1161/CIRCGEN.119.002581. Epub 2019 Aug 27.

PMID:
31454269
5.

Modulation of doxorubicin-induced expression of the multidrug resistance gene in breast cancer cells by diltiazem and protection against cardiotoxicity in experimental animals.

Al-Malky HS, Osman AM, Damanhouri ZA, Alkreathy HM, Al Aama JY, Ramadan WS, Al Qahtani AA, Al Mahdi HB.

Cancer Cell Int. 2019 Jul 24;19:191. doi: 10.1186/s12935-019-0912-0. eCollection 2019.

6.

A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family.

Gaboon NEA, Parveen A, El Beheiry A, Al-Aama JY, Alsaedi MS, Wasif N.

Front Pediatr. 2019 Jun 25;7:245. doi: 10.3389/fped.2019.00245. eCollection 2019.

7.

A mutation in the major autophagy gene, WIPI2, associated with global developmental abnormalities.

Jelani M, Dooley HC, Gubas A, Mohamoud HSA, Khan MTM, Ali Z, Kang C, Rahim F, Jan A, Vadgama N, Khan MI, Al-Aama JY, Khan A, Tooze SA, Nasir J.

Brain. 2019 May 1;142(5):1242-1254. doi: 10.1093/brain/awz075.

8.

Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation.

Alallasi SR, Kokandi AA, Banagnapali B, Shaik NA, Al-Shehri BA, Alrayes NM, Al-Aama JY, Jelani M.

Front Pediatr. 2019 Feb 21;7:44. doi: 10.3389/fped.2019.00044. eCollection 2019.

9.

Molecular Screening of VAX1 Gene Polymorphisms Uncovered the Genetic Heterogeneity of Nonsyndromic Orofacial Cleft Among Saudi Arabian Patients.

Sabbagh HJ, Innes NPT, Edris Ahmed S, Butali A, Alnamnakani EA, Rabah SM, Hamdan MA, Alhamlan NH, Abdulhameed FD, Hassan MHA, Al Mahdi HB, Alamoudi NM, Al-Aama JY, Alaki SM, Mossey PA.

Genet Test Mol Biomarkers. 2019 Jan;23(1):45-50. doi: 10.1089/gtmb.2018.0207.

PMID:
30633559
10.

Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non-Herlitz junctional epidermolysis bullosa in two paternal half-brothers from Saudi Arabia.

Al-Zahrani HS, Al-Tala S, Mohamoud HSA, Al-Shehri BA, Al-Fadhel S, Al-Qurashi A, Al-Bishri A, Al-Aama JY, Kang C, Betz RC, Jelani M.

Congenit Anom (Kyoto). 2019 May;59(3):99-101. doi: 10.1111/cga.12294. Epub 2018 Jul 6. No abstract available.

PMID:
29900604
11.

Depression and telomere length in colorectal cancer patients in Saudi Arabia.

AlAhwal MS, Zaben FA, Sehlo MG, Khalifa DA, Al-Aama JY, Edris S, Ashy JA, Koenig HG.

Asian J Psychiatr. 2019 Feb;40:130-131. doi: 10.1016/j.ajp.2018.04.039. Epub 2018 May 1. No abstract available.

PMID:
29752006
12.

A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features.

Mohamoud HS, Ahmed S, Jelani M, Alrayes N, Childs K, Vadgama N, Almramhi MM, Al-Aama JY, Goodbourn S, Nasir J.

Sci Rep. 2018 Feb 1;8(1):2053. doi: 10.1038/s41598-018-20658-w.

13.

Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

Bdier AY, Al-Ghamdi S, Verma PK, Dagriri K, Alshehri B, Jiman OA, Ahmed SE, Wilde AAM, Bhuiyan ZA, Al-Aama JY.

Mol Genet Genomic Med. 2017 Jun 21;5(5):592-601. doi: 10.1002/mgg3.305. eCollection 2017 Sep.

14.

Erratum: Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia.

Gaboon NEA, Bakur KH, Edrees AY, Al-Aama JY.

J Pediatr Genet. 2017 Sep;6(3):e1. doi: 10.1055/s-0037-1603198. Epub 2017 May 10.

15.

Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia.

A Gaboon NE, Bakur KH, Edrees AY, Al-Aama JY.

J Pediatr Genet. 2017 Sep;6(3):149-154. doi: 10.1055/s-0037-1600131. Epub 2017 Mar 16. Erratum in: J Pediatr Genet. 2017 Sep;6(3):e1.

16.

Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patients.

Al-Aama JY, Shaik NA, Banaganapalli B, Salama MA, Rashidi O, Sahly AN, Mohsen MO, Shawoosh HA, Shalabi HA, Edreesi MA, Alharthi SE, Wang J, Elango R, Saadah OI.

PLoS One. 2017 May 15;12(5):e0176664. doi: 10.1371/journal.pone.0176664. eCollection 2017.

17.

Ramadan fasting in Saudi Arabia is associated with altered expression of CLOCK, DUSP and IL-1alpha genes, as well as changes in cardiometabolic risk factors.

Ajabnoor GM, Bahijri S, Shaik NA, Borai A, Alamoudi AA, Al-Aama JY, Chrousos GP.

PLoS One. 2017 Apr 6;12(4):e0174342. doi: 10.1371/journal.pone.0174342. eCollection 2017.

18.

Novel splice site mutation in EIF2AK3 gene causes Wolcott-Rallison syndrome in a consanguineous family from Saudi Arabia.

Al-Aama JY, Al-Zahrani HS, Jelani M, Sabir HS, Al-Saeedi SA, Ahmed S.

Congenit Anom (Kyoto). 2018 Jan;58(1):39-40. doi: 10.1111/cga.12217. Epub 2017 Mar 29. No abstract available.

PMID:
28220546
19.

Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism.

Reynolds JJ, Bicknell LS, Carroll P, Higgs MR, Shaheen R, Murray JE, Papadopoulos DK, Leitch A, Murina O, Tarnauskaitė Ž, Wessel SR, Zlatanou A, Vernet A, von Kriegsheim A, Mottram RM, Logan CV, Bye H, Li Y, Brean A, Maddirevula S, Challis RC, Skouloudaki K, Almoisheer A, Alsaif HS, Amar A, Prescott NJ, Bober MB, Duker A, Faqeih E, Seidahmed MZ, Al Tala S, Alswaid A, Ahmed S, Al-Aama JY, Altmüller J, Al Balwi M, Brady AF, Chessa L, Cox H, Fischetto R, Heller R, Henderson BD, Hobson E, Nürnberg P, Percin EF, Peron A, Spaccini L, Quigley AJ, Thakur S, Wise CA, Yoon G, Alnemer M, Tomancak P, Yigit G, Taylor AM, Reijns MA, Simpson MA, Cortez D, Alkuraya FS, Mathew CG, Jackson AP, Stewart GS.

Nat Genet. 2017 Apr;49(4):537-549. doi: 10.1038/ng.3790. Epub 2017 Feb 13.

20.

Comprehensive Computational Analysis of GWAS Loci Identifies CCR2 as a Candidate Gene for Celiac Disease Pathogenesis.

Banaganapalli B, Rashidi O, Saadah OI, Wang J, Khan IA, Al-Aama JY, Shaik NA, Elango R.

J Cell Biochem. 2017 Aug;118(8):2193-2207. doi: 10.1002/jcb.25864. Epub 2017 Apr 18.

PMID:
28059456
21.

Shotgun Metagenomics of 250 Adult Twins Reveals Genetic and Environmental Impacts on the Gut Microbiome.

Xie H, Guo R, Zhong H, Feng Q, Lan Z, Qin B, Ward KJ, Jackson MA, Xia Y, Chen X, Chen B, Xia H, Xu C, Li F, Xu X, Al-Aama JY, Yang H, Wang J, Kristiansen K, Wang J, Steves CJ, Bell JT, Li J, Spector TD, Jia H.

Cell Syst. 2016 Dec 21;3(6):572-584.e3. doi: 10.1016/j.cels.2016.10.004. Epub 2016 Nov 3.

22.

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly.

Jerber J, Zaki MS, Al-Aama JY, Rosti RO, Ben-Omran T, Dikoglu E, Silhavy JL, Caglar C, Musaev D, Albrecht B, Campbell KP, Willer T, Almuriekhi M, Çağlayan AO, Vajsar J, Bilgüvar K, Ogur G, Abou Jamra R, Günel M, Gleeson JG.

Am J Hum Genet. 2016 Nov 3;99(5):1181-1189. doi: 10.1016/j.ajhg.2016.09.007. Epub 2016 Oct 20.

23.

Whole-exome sequencing reveals a recurrent mutation in the cathepsin C gene that causes Papillon-Lefevre syndrome in a Saudi family.

Alkhiary YM, Jelani M, Almramhi MM, Mohamoud HS, Al-Rehaili R, Al-Zahrani HS, Serafi R, Yang H, Al-Aama JY.

Saudi J Biol Sci. 2016 Sep;23(5):571-6. doi: 10.1016/j.sjbs.2015.06.007. Epub 2015 Jun 16.

24.

A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family.

Jelani M, Kang C, Mohamoud HS, Al-Rehaili R, Almramhi MM, Serafi R, Yang H, Al-Aama JY, Naeem M, Alkhiary YM.

Arch Oral Biol. 2016 Jul;67:28-33. doi: 10.1016/j.archoralbio.2016.03.012. Epub 2016 Mar 23.

PMID:
27019138
25.

The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family.

Alrayes N, Mohamoud HS, Ahmed S, Almramhi MM, Shuaib TM, Wang J, Al-Aama JY, Everett K, Nasir J, Jelani M.

J Neurol Sci. 2016 Apr 15;363:240-4. doi: 10.1016/j.jns.2016.02.063. Epub 2016 Mar 2.

PMID:
27000257
26.

Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients.

Saadah OI, Shaik NA, Banaganapalli B, Salama MA, Al-Harthi SE, Wang J, Shawoosh HA, Alghamdi SA, Bin-Taleb YY, Alhussaini BH, Elango R, Al-Aama JY.

Dis Markers. 2015;2015:351673. doi: 10.1155/2015/351673. Epub 2015 Dec 30.

27.

A Computational Protein Phenotype Prediction Approach to Analyze the Deleterious Mutations of Human MED12 Gene.

Banaganapalli B, Mohammed K, Khan IA, Al-Aama JY, Elango R, Shaik NA.

J Cell Biochem. 2016 Sep;117(9):2023-35. doi: 10.1002/jcb.25499. Epub 2016 Feb 10.

PMID:
26813965
28.

Effect of Ramadan fasting in Saudi Arabia on serum bone profile and immunoglobulins.

Bahijri SM, Ajabnoor GM, Borai A, Al-Aama JY, Chrousos GP.

Ther Adv Endocrinol Metab. 2015 Oct;6(5):223-32. doi: 10.1177/2042018815594527.

29.

Environmental Risk Factors in the Etiology of Nonsyndromic Orofacial Clefts in the Western Region of Saudi Arabia.

Sabbagh HJ, Alamoudi NM, Abdulhameed FD, Innes NP, Al-Aama JY, Hummaida T, Almalik M, El Derwi DA, Mossey PA.

Cleft Palate Craniofac J. 2016 Jul;53(4):435-43. doi: 10.1597/14-136. Epub 2015 Sep 24.

PMID:
26402721
30.

Birth prevalence of non-syndromic orofacial clefts in Saudi Arabia and the effects of parental consanguinity.

Sabbagh HJ, Innes NP, Sallout BI, Alamoudi NM, Hamdan MA, Alhamlan N, Al-Khozami AI, Abdulhameed FD, Al-Aama JY, Mossey PA.

Saudi Med J. 2015 Sep;36(9):1076-83. doi: 10.15537/smj.2015.9.11823.

31.

The oral and gut microbiomes are perturbed in rheumatoid arthritis and partly normalized after treatment.

Zhang X, Zhang D, Jia H, Feng Q, Wang D, Liang D, Wu X, Li J, Tang L, Li Y, Lan Z, Chen B, Li Y, Zhong H, Xie H, Jie Z, Chen W, Tang S, Xu X, Wang X, Cai X, Liu S, Xia Y, Li J, Qiao X, Al-Aama JY, Chen H, Wang L, Wu QJ, Zhang F, Zheng W, Li Y, Zhang M, Luo G, Xue W, Xiao L, Li J, Chen W, Xu X, Yin Y, Yang H, Wang J, Kristiansen K, Liu L, Li T, Huang Q, Li Y, Wang J.

Nat Med. 2015 Aug;21(8):895-905. doi: 10.1038/nm.3914. Epub 2015 Jul 27.

PMID:
26214836
32.

BRAF gene: From human cancers to developmental syndromes.

Hussain MR, Baig M, Mohamoud HS, Ulhaq Z, Hoessli DC, Khogeer GS, Al-Sayed RR, Al-Aama JY.

Saudi J Biol Sci. 2015 Jul;22(4):359-73. doi: 10.1016/j.sjbs.2014.10.002. Epub 2014 Oct 23. Review.

33.

Femoral-facial syndrome in an infant of a diabetic mother.

Ahmed S, Alsaedi SA, Al-Wassia H, Al-Aama JY.

BMJ Case Rep. 2015 Jul 6;2015. pii: bcr2014208857. doi: 10.1136/bcr-2014-208857.

34.

Truncating mutation in intracellular phospholipase A₁ gene (DDHD2) in hereditary spastic paraplegia with intellectual disability (SPG54).

Alrayes N, Mohamoud HS, Jelani M, Ahmad S, Vadgama N, Bakur K, Simpson M, Al-Aama JY, Nasir J.

BMC Res Notes. 2015 Jun 27;8:271. doi: 10.1186/s13104-015-1227-4.

35.

Identification of Two Homozygous Sequence Variants in the COL7A1 Gene Underlying Dystrophic Epidermolysis Bullosa by Whole-Exome Analysis in a Consanguineous Family.

Serafi R, Jelani M, Almramhi MM, Mohamoud HSA, Ahmed S, Alkhiary YM, Zhang J, Yang H, Al-Aama JY.

Ann Hum Genet. 2015 Sep;79(5):350-356. doi: 10.1111/ahg.12123. Epub 2015 Jun 23.

36.

Exome analysis identified a novel missense mutation in the CLPP gene in a consanguineous Saudi family expanding the clinical spectrum of Perrault Syndrome type-3.

Ahmed S, Jelani M, Alrayes N, Mohamoud HS, Almramhi MM, Anshasi W, Ahmed NA, Wang J, Nasir J, Al-Aama JY.

J Neurol Sci. 2015;353(1-2):149-54. doi: 10.1016/j.jns.2015.04.038. Epub 2015 May 1.

PMID:
25956234
37.

Case of Sjögren-Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis.

Gaboon NE, Jelani M, Almramhi MM, Mohamoud HS, Al-Aama JY.

J Dermatol. 2015 Jul;42(7):706-9. doi: 10.1111/1346-8138.12861. Epub 2015 Apr 9.

PMID:
25855245
38.

Gut microbiome development along the colorectal adenoma-carcinoma sequence.

Feng Q, Liang S, Jia H, Stadlmayr A, Tang L, Lan Z, Zhang D, Xia H, Xu X, Jie Z, Su L, Li X, Li X, Li J, Xiao L, Huber-Schönauer U, Niederseer D, Xu X, Al-Aama JY, Yang H, Wang J, Kristiansen K, Arumugam M, Tilg H, Datz C, Wang J.

Nat Commun. 2015 Mar 11;6:6528. doi: 10.1038/ncomms7528.

PMID:
25758642
39.

Novel nonsense mutation in the PTRF gene underlies congenital generalized lipodystrophy in a consanguineous Saudi family.

Jelani M, Ahmed S, Almramhi MM, Mohamoud HS, Bakur K, Anshasi W, Wang J, Al-Aama JY.

Eur J Med Genet. 2015 Apr;58(4):216-21. doi: 10.1016/j.ejmg.2015.02.002. Epub 2015 Feb 23.

PMID:
25721873
40.

Prevalence and characteristics of non-syndromic orofacial clefts and the influence of consanguinity.

Alamoudi NM, Sabbagh HJ, Innes NP, El Derwi D, Hanno AZ, Al-Aama JY, Habiballah AH, Mossey PA.

J Clin Pediatr Dent. 2014 Spring;38(3):241-6.

PMID:
25095319
41.

An integrated catalog of reference genes in the human gut microbiome.

Li J, Jia H, Cai X, Zhong H, Feng Q, Sunagawa S, Arumugam M, Kultima JR, Prifti E, Nielsen T, Juncker AS, Manichanh C, Chen B, Zhang W, Levenez F, Wang J, Xu X, Xiao L, Liang S, Zhang D, Zhang Z, Chen W, Zhao H, Al-Aama JY, Edris S, Yang H, Wang J, Hansen T, Nielsen HB, Brunak S, Kristiansen K, Guarner F, Pedersen O, Doré J, Ehrlich SD; MetaHIT Consortium, Bork P, Wang J; MetaHIT Consortium.

Nat Biotechnol. 2014 Aug;32(8):834-41. doi: 10.1038/nbt.2942. Epub 2014 Jul 6.

PMID:
24997786
42.

Health impact of fasting in Saudi Arabia during Ramadan: association with disturbed circadian rhythm and metabolic and sleeping patterns.

Ajabnoor GM, Bahijri S, Borai A, Abdulkhaliq AA, Al-Aama JY, Chrousos GP.

PLoS One. 2014 May 8;9(5):e96500. doi: 10.1371/journal.pone.0096500. eCollection 2014.

43.

First comprehensive in silico analysis of the functional and structural consequences of SNPs in human GalNAc-T1 gene.

Mohamoud HS, Hussain MR, El-Harouni AA, Shaik NA, Qasmi ZU, Merican AF, Baig M, Anwar Y, Asfour H, Bondagji N, Al-Aama JY.

Comput Math Methods Med. 2014;2014:904052. doi: 10.1155/2014/904052. Epub 2014 Mar 4.

44.

Evidence for the presence of somatic mitochondrial DNA mutations in right atrial appendage tissues of coronary artery disease patients.

Matam K, Shaik NA, Aggarwal S, Diwale S, Banaganapalli B, Al-Aama JY, Elango R, Rao P, Hasan Q.

Mol Genet Genomics. 2014 Aug;289(4):533-40. doi: 10.1007/s00438-014-0828-2. Epub 2014 Mar 7.

PMID:
24604425
45.

An induced pluripotent stem cell model of hypoplastic left heart syndrome (HLHS) reveals multiple expression and functional differences in HLHS-derived cardiac myocytes.

Jiang Y, Habibollah S, Tilgner K, Collin J, Barta T, Al-Aama JY, Tesarov L, Hussain R, Trafford AW, Kirkwood G, Sernagor E, Eleftheriou CG, Przyborski S, Stojković M, Lako M, Keavney B, Armstrong L.

Stem Cells Transl Med. 2014 Apr;3(4):416-23. doi: 10.5966/sctm.2013-0105. Epub 2014 Mar 3.

46.

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.

Novarino G, Fenstermaker AG, Zaki MS, Hofree M, Silhavy JL, Heiberg AD, Abdellateef M, Rosti B, Scott E, Mansour L, Masri A, Kayserili H, Al-Aama JY, Abdel-Salam GMH, Karminejad A, Kara M, Kara B, Bozorgmehri B, Ben-Omran T, Mojahedi F, El Din Mahmoud IG, Bouslam N, Bouhouche A, Benomar A, Hanein S, Raymond L, Forlani S, Mascaro M, Selim L, Shehata N, Al-Allawi N, Bindu PS, Azam M, Gunel M, Caglayan A, Bilguvar K, Tolun A, Issa MY, Schroth J, Spencer EG, Rosti RO, Akizu N, Vaux KK, Johansen A, Koh AA, Megahed H, Durr A, Brice A, Stevanin G, Gabriel SB, Ideker T, Gleeson JG.

Science. 2014 Jan 31;343(6170):506-511. doi: 10.1126/science.1247363.

47.

Specialty grand challenge - genetic disorders.

Al-Aama JY.

Front Pediatr. 2013 Nov 20;1:36. doi: 10.3389/fped.2013.00036. eCollection 2013. No abstract available.

48.

Variations in the GST activity are associated with single and combinations of GST genotypes in both male and female diabetic patients.

Rao DK, Shaik NA, Imran A, Murthy DK, Ganti E, Chinta C, Rao H, Shaik NS, Al-Aama JY.

Mol Biol Rep. 2014 Feb;41(2):841-8. doi: 10.1007/s11033-013-2924-5. Epub 2014 Jan 1.

PMID:
24381101
49.

Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia.

Al-Aama JY, Al-Ghamdi S, Bdier AY, AlQarawi A, Jiman OA, Al-Aama N, Al-Aata J, Wilde AA, Bhuiyan ZA.

Clin Genet. 2015;87(1):74-9. doi: 10.1111/cge.12330. Epub 2013 Dec 27.

PMID:
24372464
50.

Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies.

Eisenberger T, Neuhaus C, Khan AO, Decker C, Preising MN, Friedburg C, Bieg A, Gliem M, Charbel Issa P, Holz FG, Baig SM, Hellenbroich Y, Galvez A, Platzer K, Wollnik B, Laddach N, Ghaffari SR, Rafati M, Botzenhart E, Tinschert S, Börger D, Bohring A, Schreml J, Körtge-Jung S, Schell-Apacik C, Bakur K, Al-Aama JY, Neuhann T, Herkenrath P, Nürnberg G, Nürnberg P, Davis JS, Gal A, Bergmann C, Lorenz B, Bolz HJ.

PLoS One. 2013 Nov 12;8(11):e78496. doi: 10.1371/journal.pone.0078496. eCollection 2013. Erratum in: PLoS One. 2014;9(11):e108840.

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