HuGE Literature Finder
Records 1-30
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Maternal serum Apelin 13 and
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2021 Jan 1-9. Gandham Rajeev, Dayanand C D, Sheela S R, Kiranmayee |
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Impact of NRG1 HapICE gene variants on digit ratio and dermatoglyphic measures in schizophrenia.
Asian journal of psychiatry 2020 Dec 54 102363. Rajasekaran Ashwini, Shivakumar Venkataram, Kalmady Sunil V, Parlikar Rujuta, Chhabra Harleen, Prabhu Ananya, Subbanna Manjula, Venugopal Deepthi, Amaresha Anekal C, Agarwal Sri Mahavir, Bose Anushree, Narayanaswamy Janardhanan C, Debnath Monojit, Venkatasubramanian Ganes |
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Association of Serum Biomarker Levels and BDNF Gene Polymorphism with Response to Selective Serotonin Reuptake Inhibitors in Indian Patients with Major Depressive Disorder.
Neuropsychobiology 2020 Jul 1-13. Ramesh Varsha, Venkatesan Vettriselvi, Chellathai Darling, Silamban Sant |
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Determining the association between polymorphisms of the
Neurology international 2020 Jul 12 (1): 8292. Thursina Cempaka, Nurputra Dian Kesumapramudya, Harahap Indra Sari Kusuma, Harahap Nur Imma Fatimah, Sa'adah Nihayatus, Wibowo Samekto, Sutarni Sri, Sadewa Ahmad Hamim, Hanjaya Hermawan, Nishio Hisahi |
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Evaluation of non-coding region sequence variants and mitochondrial haplogroups as potential biomarkers of sporadic breast cancer in individuals of Sri Lankan Sinhalese ethnicity.
Biomedical reports 2020 Jun 12 (6): 339-347. Tiphania Kotelawala Joanne, Ranasinghe Ruwandi, Rodrigo Chrishani, Tennekoon Kamani Hemamala, Silva Kanishka |
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In depth analysis of the association of FTO SNP (rs9939609) with the expression of classical phenotype of PCOS: a Sri Lankan study.
BMC medical genetics 2020 Feb 21 (1): 30. Branavan Umayal, Wijesundera Sulochana, Chandrasekaran Vishvanath, Arambepola Carukshi, Wijeyaratne Chandri |
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Association of SLC1A1 gene polymorphism with obsessive compulsive disorder in a sample from southern India.
Experimental and clinical psychopharmacology 2020 Jan . Shukla Tulika, Nadella Ravi Kumar, Taj M J Reshma Jabeen, Ganesh Suhas, Nestadt Gerald, Purushottam Meera, Jain Sanjeev, Reddy Y C Janardhan, Viswanath Bi |
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Association of the leptin receptor Q223R (rs1137101) polymorphism with obesity measures in Sri Lankans.
BMC research notes 2020 Jan 13 (1): 34. Illangasekera Y A, Kumarasiri P V R, Fernando D J, Dalton C |
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Pattern of nucleotide variants of TP53 and their correlation with the expression of p53 and its downstream proteins in a Sri Lankan cohort of breast and colorectal cancer patients.
BMC cancer 2020 Jan 20 (1): 72. Manoharan Vahinipriya, Karunanayake Eric Hamilton, Tennekoon Kamani Hemamala, De Silva Sumadee, Imthikab Ahamed Ilyas Ahamed, De Silva Kanishka, Angunawela Preethika, Vishwakula Sameera, Lunec Jo |
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The Asthma-associated PER1-like domain-containing protein 1 (PERLD1) Haplotype Influences Soluble Glycosylphosphatidylinositol Anchor Protein (sGPI-AP) Levels in Serum and Immune Cell Proliferation.
Scientific reports 2020 Jan 10 (1): 715. Sio Yang Yie, Anantharaman Ramani, Lee Sean Qiu En, Matta Sri Anusha, Ng Yu Ting, Chew Fook T |
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Epistasis between Phenylethanolamine N-methyltransferase (PNMT) and ß2-adrenergic receptor (ADRB2) Influences Extracellular Epinephrine Level and Associates with the Susceptibility to Allergic Asthma.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2019 Dec . Sio Yang Yie, Matta Sri Anusha, Ng Yu Ting, Chew Fook T |
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G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population.
BMC pediatrics 2019 Dec 19 (1): 506. Wisnumurti Dewi A, Sribudiani Yunia, Porsch Robert M, Maskoen Ani M, Rahayuningsih Sri E, Asni Eni K, Sleutels Frank, van Ijcken Wilfred F J, Sukadi Abdurachman, Achmad Tri |
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Novel Arg128Ala variant in Catechol-O-methyltransferase gene influence persistent pain.
Clinical genetics 2019 Oct . Dharaniprasad Goduguchintha, Samantaray Aloka, Srikanth Lokanathan, Hanumantha Rao Mangu, Chandra Abha, Sarma Potukuchi Venktata Gurunadha Krish |
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Association of single nucleotide polymorphisms of adiponectin and leptin genes with breast cancer.
Molecular biology reports 2019 Sep . Geriki Sarvari, Bitla Aparna R, SrinivasaRao P V L N, Hulikal Narendra, Yootla Mutheeswaraiah, Sachan Alok, Amancharla Yadagiri Lakshmi, Asha T, Manickavasagam M, Kannan T, Kumari Aruna |
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Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at
Biomolecules 2019 Jul 9 (8): . Prasad Gauri, Bandesh Khushdeep, Giri Anil K, Kauser Yasmeen, Chanda Prakriti, Parekatt Vaisak, Mathur Sandeep, Madhu Sri Venkata, Venkatesh Pradeep, Bhansali Anil, Marwaha Raman K, Basu Analabha, Tandon Nikhil, Bharadwaj Dwaipayan, |
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The Correlation of
Open access Macedonian journal of medical sciences 2019 Jun 7 (12): 1940-1945. Rachmawati Meike, Yulianti Herry, Hernowo Bethy S, Suryanti Sri, Wijaya Indra, Rahadiani Nur, Heriyanto Didik S, Irianiwati Irianiwa |
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The p.H63D allele of the HFE gene protects against low iron stores in Sri Lanka.
Blood cells, molecules & diseases 2019 Feb . Allen Angela, Premawardhena Anuja, Allen Stephen, Rodrigo Rexan, Manamperi Aresha, Perera Luxman, Wray Katherine, Armitage Andrew, Fisher Christopher, Drakesmith Alexander, Robson Kathryn, Weatherall Dav |
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Association of Kiss1 and GPR54 Gene Polymorphisms with Polycystic Ovary Syndrome among Sri Lankan Women.
BioMed research international 2019 2019 6235680. Branavan Umayal, Muneeswaran Kajan, Wijesundera W S S, Senanayake Anoma, Chandrasekharan N Vishvanath, Wijeyaratne Chandrika |
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Genetic associations of inflammatory bowel disease in a South Asian population.
World journal of clinical cases 2018 Dec 6 (15): 908-915. Niriella Madunil Anuk, Liyanage Isurujith Kongala, Kodisinghe Senerath Kuleesha, Silva Arjuna Priyadarsin De, Rajapakshe Nimna, Nanayakkara Sunali D, Luke Dunya, Silva Thilakshi, Nawarathne Metthananda, Peiris Ranjith K, Kalubovila Udaya P, Kumarasena Sujeewa R, Dissanayake Vajira Harshadeva Weerabaddana, Jayasekara Rohan W, de Silva Hithanadura Jana |
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Association of G472A allele of membrane bound catechol-O-methyltransferase gene with chronic post-sternotomy pain.
General thoracic and cardiovascular surgery 2018 Aug . Dharaniprasad Goduguchintha, Samantaray Aloka, Hanumantha Rao Mangu, Chandra Abha, Sarma Potukuchi Venkata Gurunadha Krish |
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The D allele of the angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism is associated with worse functional outcome of ischaemic stroke.
The International journal of neuroscience 2018 Aug 128 (8): 697-704. Malueka Rusdy Ghazali, Dwianingsih Ery Kus, Sutarni Sri, Bawono Rheza Gandi, Bayuangga Halwan Fuad, Gofir Abdul, Setyopranoto Isma |
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Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women.
Journal of breast cancer 2018 Jun 21 (2): 165-172. Sirisena Nirmala Dushyanthi, Adeyemo Adebowale, Kuruppu Anchala Ishani, Samaranayake Nilakshi, Dissanayake Vajira Harshadeva Weerabadda |
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Pharmacogenetic evaluation of a DISP1 gene variant in antidepressant treatment of obsessive-compulsive disorder.
Human psychopharmacology 2018 Jun e2659. Lisoway Amanda J, Zai Gwyneth, Tiwari Arun K, Zai Clement C, Wigg Karen, Goncalves Vanessa, Zhang Danning, Freeman Natalie, Müller Daniel J, Kennedy James L, Richter Margaret |
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Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka.
Molecular genetics & genomic medicine 2018 May . Javadiyan Shari, Lucas Sionne E M, Wangmo Dechen, Ngy Meng, Edussuriya Kapila, Craig Jamie E, Rudkin Adam, Casson Robert, Selva Dinesh, Sharma Shiwani, Lower Karen M, Meucke James, Burdon Kathryn |
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Spectrum of low-density lipoprotein receptor (LDLR) mutations in a cohort of Sri Lankan patients with familial hypercholesterolemia - a preliminary report.
Lipids in health and disease 2018 May 17 (1): 100. Paththinige C S, Rajapakse J R D K, Constantine G R, Sem K P, Singaraja R R, Jayasekara R W, Dissanayake V H |
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Gene polymorphisms and response to transcranial direct current stimulation for auditory verbal hallucinations in schizophrenia.
Acta neuropsychiatrica 2018 Mar 1-8. Chhabra Harleen, Shivakumar Venkataram, Subbanna Manjula, Kalmady Sunil V, Bose Anushree, Agarwal Sri Mahavir, Sreeraj Vanteemar S, Dinakaran Damodharan, Narayanaswamy Janardhanan C, Debnath Monojit, Venkatasubramanian Ganes |
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UGT1A1
Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.
BioMed research international 2018 2018 9425843. Wisnumurti Dewi A, Sribudiani Yunia, Porsch Robert M, Maskoen Ani M, Abdulhamied Lola I, Rahayuningsih Sri E, Asni Eni K, Sleutels Frank, Kockx Christel E M, van Ijcken Wilfred F J, Sukadi Abdurachman, Achmad Tri |
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Genetic determinants of sporadic breast cancer in Sri Lankan women.
BMC cancer 2018 02 18 (1): 180. Sirisena Nirmala Dushyanthi, Adeyemo Adebowale, Kuruppu Anchala I, Neththikumara Nilaksha, Samaranayake Nilakshi, Dissanayake Vajira H |
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Genetic variation of GRIA3 gene is associated with vulnerability to methamphetamine dependence and its associated psychosis.
Journal of psychopharmacology (Oxford, England) 2018 03 32 (3): 309-315. Iamjan Sri-Arun, Thanoi Samur, Watiktinkorn Paritat, Reynolds Gavin P, Nudmamud-Thanoi Suti |
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Serum 25-hydroxyvitamin D, serum calcium and vitamin D receptor (VDR) polymorphisms in a selected population with lumbar disc herniation-A case control study.
PloS one 2018 13 (10): e0205841. Withanage Niroshima Dedunu, Perera Sunil, Peiris Hemantha, Athiththan Lohini Vijayendr |
- Page last reviewed:Oct 1, 2020
- Page last updated:Jan 27, 2021
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