15 research outputs found
Effect of cropping system and age of plant at harvest on tuber rot and performance of elite cassava varieties in derived savannah
- Author
- Publication venue
- 'Biotechnical Faculty'
- Publication date
- Field of study
Effect of cropping system and age of plant at harvest on tuber rot and performance of elite cassava varieties in derived savannah
- Author
- Publication venue
- 'Biotechnical Faculty'
- Publication date
- 01/09/2017
- Field of study
Devastated tuber rot disease among farmers prompted the evaluation of the elite improved varieties in the intercrop and the practice of delaying harvesting when there is glut in the market necessitated this study. Trial was carried out at the Federal University of Agriculture, Abeokuta between 2011 and 2014 to evaluate yield performance of 21 elite cassava varieties planted as sole crop verse intercropped and harvested at different age. The 2 x 21 x 3 factorial experiment was laid out in randomized complete block design and replicated three times. The tuber yield obtained from sole plot in 2011/2012 cropping season was significantly higher than intercrop whereas those of 2012/2014 cropping season were similar. Land Equivalent Ratio was above one in both cropping seasons indicating that the performance of the improved varieties in intercrop was efficient. The pooled mean tuber yield showed that TMS 30572, 92/0326, 95/0211, 01/1371, 00/0338, 01/0046, 00/0098, 01/1097, 01/0085, 98/0581 and 98/510 were among the top eight varieties. Harvesting could be delayed up to 15 months after planting to reduce tuber rot
Whole-genome sequencing reveals host factors underlying critical COVID-19
- Author
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2022
- Field of study
Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2–4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease
Whole-genome sequencing reveals host factors underlying critical COVID-19
- Author
- Abd Elghafar M.S.
- Abdel-Aziz M.
- Abdelrazik M.
- Abdollahi H.
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- Zöllner S.
- Åsvold B.O.
- Publication venue
- Springer Science and Business Media LLC
- Publication date
- 07/07/2022
- Field of study
Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease
Global, regional, and national burden of disorders affecting the nervous system, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021
- Author
- Abate Yohannes Habtegiorgis
- Abbas Jaffar
- Abbasi Madineh Akram
- Abbasian Mohammadreza
- Abbastabar Hedayat
- Abd-Rabu Rami
- Abdelmasseh Michael
- Abdollahi Mohammad
- Abdollahi Mozhan
- Abdollahifar Mohammad-Amin
- Abdulah Deldar Morad
- Abdullahi Auwal
- Abedi Aidin
- Abedi Vida
- Abeldaño Zuñiga Roberto Ariel
- Abidi Hassan
- Abiodun Olumide
- Aboagye Richard Gyan
- Abolhassani Hassan
- Aboyans Victor
- Abrha Woldu Aberhe
- Abu-Gharbieh Eman
- Abualhasan Ahmed
- Aburuz Salahdein
- Adamu Lawan Hassan
- Addo Isaac Yeboah
- Adebayo Oladimeji M
- Adekanmbi Victor
- Adekiya Tayo Alex
- Adikusuma Wirawan
- Adnani Qorinah Estiningtyas Sakilah
- Adra Saryia
- Afework Tsion
- Afolabi Aanuoluwapo Adeyimika
- Afraz Ali
- Afzal Saira
- Aghamiri Shahin
- Agodi Antonella
- Agyemang-Duah Williams
- Ahinkorah Bright Opoku
- Ahmad Aqeel
- Ahmad Danish
- Ahmad Sajjad
- Ahmadzade Amir Mahmoud
- Ahmed Ali
- Ahmed Ayman
- Ahmed Haroon
- Ahmed Jivan Qasim
- Ahmed Luai A
- Ahmed Muktar Beshir
- Ahmed Syed Anees
- Ajami Marjan
- Aji Budi
- Ajumobi Olufemi
- Akade Seyed Esma'il
- Akbari Morteza
- Akbarialiabad Hossein
- Akhlaghi Shiva
- Akinosoglou Karolina
- Akinyemi Rufus Olusola
- Akonde Maxwell
- Al Hasan Syed Mahfuz
- AL-Ahdal Tareq Mohammed Ali
- Al-amer Rasmieh Mustafa
- Al-Gheethi Adel Ali Saeed
- Al-Omari Basem
- Al-Shahi Salman Rustam
- Al-Tawfiq Jaffar A
- Al-Worafi Yaser Mohammed
- Alahdab Fares
- Albashtawy Mohammed
- AlBataineh Mohammad T
- Aldawsari Khalifah A
- Alemi Hediyeh
- Alemi Sharifullah
- Algammal Abdelazeem M
- Alhalaiqa Fadwa Alhalaiqa Naji
- Alhassan Robert Kaba
- Ali Abid
- Ali Endale Alemayehu
- Ali Liaqat
- Ali Mohammed Usman
- Ali Musa Mohammed
- Ali Rafat
- Ali Shahid
- Ali Syed Shujait Shujait
- Ali Zahid
- Alif Sheikh Mohammad
- Alimohamadi Yousef
- Aliyi Ahmednur Adem
- Aljofan Mohamad
- Aljunid Syed Mohamed
- Alladi Suvarna
- Almazan Joseph Uy
- Almustanyir Sami
- Alqahtani Jaber S
- Alqasmi Ibrahim
- Alqutaibi Ahmed Yaseen
- Altaany Zaid
- Altirkawi Khalid A
- Alvis-Guzman Nelson
- Aly Hany
- Aly Safwat
- Alzoubi Karem H
- Amani Reza
- Amindarolzarbi Alireza
- Amiri Sohrab
- Amirzade-Iranaq Mohammad Hosein
- Amu Hubert
- Amugsi Dickson A
- Amusa Ganiyu Adeniyi
- Amzat Jimoh
- Ancuceanu Robert
- Anderlini Deanna
- Anderson David B
- Andrei Catalina Liliana
- Androudi Sofia
- Angappan Dhanalakshmi
- Angesom Teklit W
- Anil Abhishek
- Ansari-Moghaddam Alireza
- Anwer Razique
- Arafat Mosab
- Aravkin Aleksandr Y
- Areda Demelash
- Ariffin Hany
- Arifin Hidayat
- Arkew Mesay
- Arooj Mahwish
- Artamonov Anton A
- Artanti Kurnia Dwi
- Aruleba Raphael Taiwo
- Asadi-Pooya Ali A
- Asena Tilahun Ferede
- Asghari-Jafarabadi Mohammad
- Ashraf Muhammad
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- Athari Seyyed Shamsadin
- Atinafu Bantalem Tilaye Tilaye
- Atorkey Prince
- Atout Maha Moh'd Wahbi
- Atreya Alok
- Aujayeb Avinash
- Avan Abolfazl
- Ayala Quintanilla Beatriz Paulina
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- Banerjee Indrajit
- Baran Mehmet Firat
- Barboza Miguel A
- Barchitta Martina
- Bardhan Mainak
- Barker-Collo Suzanne Lyn
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- Bashash Davood
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- Basu Sanjay
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- Bedi Neeraj
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- Begum Tahmina
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- Biswas Atanu
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- Bustanji Yasser
- Butt Muhammad Hammad
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- Butt Zahid A
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- Caetano dos Santos Florentino Luciano
- Calina Daniela
- Campos-Nonato Ismael R
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- Cerin Ester
- Chacón-Uscamaita Pamela R Uscamaita
- Chan Jeffrey Shi Kai
- Chanie Gashaw Sisay
- Charan Jaykaran
- Chattu Vijay Kumar
- Chekol Abebe Endeshaw
- Chen Hui
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- Chi Gerald
- Chichagi Fatemeh
- Chidambaram Saravana Babu
- Chimoriya Ritesh
- Ching Patrick R
- Chitheer Abdulaal
- Chong Yuen Yu
- Chopra Hitesh
- Choudhari Sonali Gajanan
- Chowdhury Enayet Karim
- Chowdhury Rajiv
- Christensen Hanne
- Chu Dinh-Toi
- Chukwu Isaac Sunday
- Chung Eric
- Coberly Kaleb
- Columbus Alyssa
- Comachio Josielli
- Conde Joao
- Cortesi Paolo Angelo
- Costa Vera Marisa
- Cousin Ewerton
- Couto Rosa A S
- Criqui Michael H
- Cruz-Martins Natália
- Cárdenas Rosario
- D'Amico Emanuele
- Dabbagh Ohadi Mohammad Amin
- Dadana Sriharsha
- Dadras Omid
- Dai Xiaochen
- Dai Zhaoli
- Danawi Hadi A
- Dandona Lalit
- Dandona Rakhi
- Darwish Amira Hamed
- Das Saswati
- Das Subasish
- Dascalu Ana Maria
- Dash Nihar Ranjan
- Dashti Mohsen
- De la Hoz Fernando Pio
- de la Torre-Luque Alejandro
- De Leo Diego
- Dean Frances E
- Dehghan Amin
- Dehghan Azizallah
- Dejene Hiwot
- Demant Daniel
- Demetriades Andreas K
- Demissie Solomon
- Deng Xinlei
- Desai Hardik Dineshbhai
- Devanbu Vinoth Gnana Chellaiyan
- Dhama Kuldeep
- Dharmaratne Samath Dhamminda
- Dhimal Meghnath
- Dias da Silva Diana
- Diaz Daniel
- Dibas Mahmoud
- Ding Delaney D
- Dinu Monica
- Dirac M Ashworth
- Diress Mengistie
- Do Thanh Chi
- Do Thao Huynh Phuong
- Doan Khanh Duy Khanh
- Dodangeh Milad
- Doheim Mohamed Fahmy
- Dokova Klara Georgieva
- Dongarwar Deepa
- Dsouza Haneil Larson
- Dua Tarun
- Dube John
- Duraisamy Senbagam
- Durojaiye Oyewole Christopher
- Dutta Sulagna
- Dziedzic Arkadiusz Marian
- Edinur Hisham Atan
- Eissazade Negin
- Ekholuenetale Michael
- Ekundayo Temitope Cyrus
- El Nahas Nevine
- El Sayed Iman
- Elahi Najafi Mohammad Amin
- Elbarazi Iffat
- Elemam Noha Mousaad
- Elgar Frank J
- Elgendy Islam Y
- Elhabashy Hala Rashad
- Elhadi Muhammed
- Elilo Legesse Tesfaye
- Ellenbogen Richard G
- Elmeligy Omar Abdelsadek Abdou
- Elmonem Mohamed A
- Elshaer Mohammed
- Elsohaby Ibrahim
- Emamverdi Mehdi
- Emeto Theophilus I
- Endres Matthias
- Esezobor Christopher Imokhuede
- Eskandarieh Sharareh
- Fadaei Abdolmajid
- Fagbamigbe Adeniyi Francis
- Fahim Ayesha
- Faramarzi Ali
- Fares Jawad
- Farjoud Kouhanjani Mohsen
- Faro Andre
- Farzadfar Farshad
- Fatehizadeh Ali
- Fathi Mobina
- Fathi Saeid
- Fatima Syeda Anum Fatima
- Feigin Valery L
- Feizkhah Alireza
- Fereshtehnejad Seyed-Mohammad
- Ferrari Alize J
- Ferreira Nuno
- Fetensa Getahun
- Firouraghi Neda
- Fischer Florian
- Fonseca Ana Catarina
- Force Lisa M
- Fornari Arianna
- Foroutan Behzad
- Fukumoto Takeshi
- Gadanya Muktar A
- Gaidhane Abhay Motiramji
- Galali Yaseen
- Galehdar Nasrin
- Gan Quan
- Gandhi Aravind P
- Ganesan Balasankar
- Gardner William M
- Garg Naval
- Gau Shuo-Yan
- Gautam Rupesh K
- Gebre Teshome
- Gebrehiwot Mesfin
- Gebremeskel Gebreamlak Gebremedhn
- Gebreslassie Haftay Gebremedhin
- Getacher Lemma
- Ghaderi Yazdi Bardiya
- Ghadirian Fataneh
- Ghaffarpasand Fariborz
- Ghanbari Reza
- Ghasemi MohammadReza
- Ghazy Ramy Mohamed
- Ghimire Sailaja
- Gholami Ali
- Gholamrezanezhad Ali
- Ghotbi Elena
- Ghozy Sherief
- Gialluisi Alessandro
- Gill Paramjit Singh
- Glasstetter Logan M
- Gnedovskaya Elena V
- Golchin Ali
- Golechha Mahaveer
- Goleij Pouya
- Golinelli Davide
- Gomes-Neto Mansueto
- Goulart Alessandra C
- Goyal Anmol
- Gray Richard J
- Grivna Michal
- Guadie Habtamu Alganeh
- Guan Bin
- Guarducci Giovanni
- Guicciardi Stefano
- Gunawardane Damitha Asanga
- Guo Hanbing
- Gupta Bhawna
- Gupta Rajeev
- Gupta Sapna
- Gupta Veer Bala
- Gupta Vivek Kumar
- Gutiérrez Reyna Alma
- Habibzadeh Farrokh
- Hachinski Vladimir
- Haddadi Rasool
- Hadei Mostafa
- Hadi Najah R
- Haep Nils
- Hagins Hailey
- Haile Teklehaimanot Gereziher
- Haj-Mirzaian Arvin
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- Halwani Rabih
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- Hammoud Ahmad
- Han Hannah
- Hanifi Nasrin
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- Hannan Md. Abdul
- Hao Junwei
- Harapan Harapan
- Hareru Habtamu Endashaw
- Hargono Arief
- Harlianto Netanja I.
- Haro Josep Maria
- Hartman Nicholas Nathaniel
- Hasaballah Ahmed I.
- Hasan Faizul
- Hasani Hamidreza
- Hasanian Mohammad
- Hassan Amr
- Hassan Shoaib
- Hassanipour Soheil
- Hassankhani Hadi
- Hassen Mohammed Bheser
- Haubold Johannes
- Hay Simon I
- Hayat Khezar
- Hegazy Mohamed I
- Heidari Golnaz
- Heidari Mohammad
- Heidari-Soureshjani Reza
- Hesami Hamed
- Hezam Kamal
- Hiraike Yuta
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- Holla Ramesh
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- Hostiuc Sorin
- Hu Chengxi
- Huang Junjie
- Huda Md. Nazmul
- Hussain Javid
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- khorashadizadeh Fatemeh
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- Prakash Peralam Yegneswaran
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- Prates Elton Junio Sady
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- Purnobasuki Hery
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- Rahmani Amir Masoud
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- Raj Moolambally Sheetal
- Rajabpour-Sanati Ali
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- Razo Christian
- Redwan Elrashdy Moustafa Mohamed
- Rekabi Bana Atefe
- Remuzzi Giuseppe
- Rezaei Nazila
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- Saeed Umar
- Saeed Usman
- Safdarian Mahdi
- Safi Sher Zaman
- Sagar Rajesh
- Sagoe Dominic
- Saheb Sharif-Askari Fatemeh
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- Servili Chiara
- Sethi Yashendra
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- Seylani Allen
- Shabani Mohammad
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- Tesfaye Amensisa Hailu
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- Thakali Ocean
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- Tsegay Guesh Mebrahtom
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- Ubah Chukwudi S
- Udoakang Aniefiok John
- Ulhaq Inam
- Umair Muhammad
- Umakanthan Srikanth
- Umapathi Krishna Kishore
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- Unnikrishnan Bhaskaran
- Vaithinathan Asokan Govindaraj
- Vakilian Alireza
- Valadan Tahbaz Sahel
- Valizadeh Rohollah
- Van den Eynde Jef
- Vart Priya
- Varthya Shoban Babu
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- Vaziri Siavash
- Vellingiri Balachandar
- Venketasubramanian Narayanaswamy
- Verras Georgios-Ioannis
- Vervoort Dominique
- Villafañe Jorge Hugo
- Villani Leonardo
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- Vu Loc Tri
- Vujcic Isidora S
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- Waris Abdul
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- Weintraub Robert G
- Weldemariam Abrha Hailay
- Westerman Ronny
- Whisnant Joanna L
- Wickramasinghe Dakshitha Praneeth
- Wickramasinghe Nuwan Darshana
- Willekens Barbara
- Wilner Lauren B
- Winkler Andrea Sylvia
- Wolfe Charles D A
- Wu Ai-Min
- Wulf Hanson Sarah
- Xu Suowen
- Xu Xiaoyue
- Yadollahpour Ali
- Yaghoubi Sajad
- Yahya Galal
- Yamagishi Kazumasa
- Yang Lin
- Yano Yuichiro
- Yao Yao
- Yehualashet Sisay Shewasinad
- Yeshaneh Alex
- Yesiltepe Metin
- Yi Siyan
- Yiğit Arzu
- Yiğit Vahit
- Yon Dong Keon
- Yonemoto Naohiro
- You Yuyi
- Younis Mustafa Z
- Yu Chuanhua
- Yusuf Hadiza
- Zadey Siddhesh
- Zahedi Mohammad
- Zakham Fathiah
- Zaki Nazar
- Zali Alireza
- Zamagni Giulia
- Zand Ramin
- Zandieh Ghazal G Z
- Zangiabadian Moein
- Zarghami Amin
- Zastrozhin Mikhail Sergeevich
- Zeariya Mohammed G M
- Zegeye Zelalem Banjaw
- Zeukeng Francis
- Zhai Chunxia
- Zhang Chen
- Zhang Haijun
- Zhang Yunquan
- Zhang Zhi-Jiang
- Zhao Hanqing
- Zhao Yang
- Zheng Peng
- Zhou Hengxing
- Zhu Bin
- Zhumagaliuly Abzal
- Zielińska Magdalena
- Zikarg Yossef Teshome
- Zoladl Mohammad
- Ärnlöv Johan
- Publication venue
- Elsevier
- Publication date
- 01/04/2024
- Field of study
BackgroundDisorders affecting the nervous system are diverse and include neurodevelopmental disorders, late-life neurodegeneration, and newly emergent conditions, such as cognitive impairment following COVID-19. Previous publications from the Global Burden of Disease, Injuries, and Risk Factor Study estimated the burden of 15 neurological conditions in 2015 and 2016, but these analyses did not include neurodevelopmental disorders, as defined by the International Classification of Diseases (ICD)-11, or a subset of cases of congenital, neonatal, and infectious conditions that cause neurological damage. Here, we estimate nervous system health loss caused by 37 unique conditions and their associated risk factors globally, regionally, and nationally from 1990 to 2021.MethodsWe estimated mortality, prevalence, years lived with disability (YLDs), years of life lost (YLLs), and disability-adjusted life-years (DALYs), with corresponding 95% uncertainty intervals (UIs), by age and sex in 204 countries and territories, from 1990 to 2021. We included morbidity and deaths due to neurological conditions, for which health loss is directly due to damage to the CNS or peripheral nervous system. We also isolated neurological health loss from conditions for which nervous system morbidity is a consequence, but not the primary feature, including a subset of congenital conditions (ie, chromosomal anomalies and congenital birth defects), neonatal conditions (ie, jaundice, preterm birth, and sepsis), infectious diseases (ie, COVID-19, cystic echinococcosis, malaria, syphilis, and Zika virus disease), and diabetic neuropathy. By conducting a sequela-level analysis of the health outcomes for these conditions, only cases where nervous system damage occurred were included, and YLDs were recalculated to isolate the non-fatal burden directly attributable to nervous system health loss. A comorbidity correction was used to calculate total prevalence of all conditions that affect the nervous system combined.FindingsGlobally, the 37 conditions affecting the nervous system were collectively ranked as the leading group cause of DALYs in 2021 (443 million, 95% UI 378–521), affecting 3·40 billion (3·20–3·62) individuals (43·1%, 40·5–45·9 of the global population); global DALY counts attributed to these conditions increased by 18·2% (8·7–26·7) between 1990 and 2021. Age-standardised rates of deaths per 100 000 people attributed to these conditions decreased from 1990 to 2021 by 33·6% (27·6–38·8), and age-standardised rates of DALYs attributed to these conditions decreased by 27·0% (21·5–32·4). Age-standardised prevalence was almost stable, with a change of 1·5% (0·7–2·4). The ten conditions with the highest age-standardised DALYs in 2021 were stroke, neonatal encephalopathy, migraine, Alzheimer's disease and other dementias, diabetic neuropathy, meningitis, epilepsy, neurological complications due to preterm birth, autism spectrum disorder, and nervous system cancer.InterpretationAs the leading cause of overall disease burden in the world, with increasing global DALY counts, effective prevention, treatment, and rehabilitation strategies for disorders affecting the nervous system are needed
Identification, assessment of diseases and agronomic parameters of Curcuma amada Roxb (Mango ginger)
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/11/2018
- Field of study
Many diseases affect plants, causing physiological dysfunctions and structural deviation from normal. The effects of plant diseases on yield and quality of crops have been documented. Little, however, is known about the pathology and agronomy of Mango ginger (Curcuma amada Roxb.), an under-cultivated crop. The present study was carried out to assess disease incidence and severity of associated fungal diseases of Mango ginger; assess rhizome yield loss due to disease; isolate and identify fungal pathogens associated; evaluate growth parameters of Mango ginger. Mango ginger plants began showing symptoms of leaf spot and leaf blight at first week and at fifth week after emergence, respectively; at twenty-fourth week some rhizomes were visually observed to be affected with rot. Cercospora curcumae, Phyllosticta zingiberi and Colletotrichum capsici; C. gloeosporioides, Alternaria alternata and Rhizoctonia solani; R. solani, Fusarium solani and Pythium aphanidermatum were frequently found associated with leaf spot, leaf blight and rhizome rot, respectively. Correlation coefficient of: Spot Disease Incidence with plant height was −0.04 and −0.05 for 2016 and 2017, respectively; number of leaves in progression with age was significant at p < 0.01 in 2016 (0.63) but insignificant in 2017 (0.32). Also, correlation coefficient of Blight Disease Incidence: with plant height was significant at p < 0.01 in the year 2016 (0.94) and 2017 (0.92); with number of leaves as age progressed was 0.54 and 0.70 for 2016 and 2017, respectively, and significant at p < 0.01. Percentage losses of 3.25 and 3.02, at harvest, due to rhizome rot were recorded for 2016 and 2017, respectively. This study revealed the occurrence of diseases, associated with fungi and fungus-like organisms, and their effect on Mango ginger plants. Keywords: Mango ginger (Curcuma amada Roxb.), Leaf spot, Leaf blight, Rhizome rot, Fungal disease
Response of lowland rice-ratooned rice-fluted pumpkin sequence to fertilizer in rainfed inland valley in derived savannah of Nigeria
- Author
- Publication venue
- 'Biotechnical Faculty'
- Publication date
- 01/01/2017
- Field of study
Trial was carried out at Federal University of Agriculture, Abeokuta, Nigeria between 2010 and 2012 to determine response of lowland rice-ratooned rice-fluted pumpkin sequence to fertilizer. Experiment was laid out in Randomized Complete Block Design arranged in split-split plot in three replicates. Three rice genotypes constituted the main treatments sown in May and harvested in August. Split fertilizers application constituted sub-plot treatments were 90:45:45 (single dose), 45:22.5:22.5 & 45:22.5:22.5 (1:1), 30:15:15 & 60:30:30 (1:2) and 60:30:30 & 30:15:15 (2:1) NPK ha-1 at tillering and heading. N-fertilizer rates were sub-sub plot treatment and applied to ratooned ‘NERICA L-42’ had the tallest plants compare to others. ‘Ofada’ had the lowest number of days to 50 % flowering for main and ratooned rice, while ‘NERICA L-42’ had the highest number of days to 50 % heading. ‘NERICA L-41’ variety had the highest grain yield in main and ratooned rice. Based on this study, ‘NERICA L-41’ plus its ratooned rice obtained from single dose NPK and zero N-fertilizer plots produced grain yield of 4.69 t ha-1.</p
Mapping the human genetic architecture of COVID-19
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- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2021
- Field of study
The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-191,2, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases3–7. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease
Recommended from our members
GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
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- Publication venue
- Springer Nature
- Publication date
- 17/05/2023
- Field of study
Data availability: Downloadable summary data are available through the GenOMICC data site (https://genomicc.org/data). Summary statistics are available, but without the 23andMe summary statistics, except for the 10,000 most significant hits, for which full summary statistics are available. The full GWAS summary statistics for the 23andMe discovery dataset will be made available through 23andMe to qualified researchers under an agreement with 23andMe that protects the privacy of the 23andMe participants. For further information and to apply for access to the data, see the 23andMe website (https://research.23andMe.com/dataset-access/). All individual-level genotype and whole-genome sequencing data (for both academic and commercial uses) can be accessed through the UKRI/HDR UK Outbreak Data Analysis Platform (https://odap.ac.uk). A restricted dataset for a subset of GenOMICC participants is also available through the Genomics England data service. Monocyte RNA-seq data are available under the title ‘Monocyte gene expression data’ within the Oxford University Research Archives (https://doi.org/10.5287/ora-ko7q2nq66). Sequencing data will be made freely available to organizations and researchers to conduct research in accordance with the UK Policy Framework for Health and Social Care Research through a data access agreement. Sequencing data have been deposited at the European Genome–Phenome Archive (EGA), which is hosted by the EBI and the CRG, under accession number EGAS00001007111.Extended data figures and tables are available online at https://www.nature.com/articles/s41586-023-06034-3#Sec21 .Supplementary information is available online at https://www.nature.com/articles/s41586-023-06034-3#Sec22 .Code availability:
Code to calculate the imputation of P values on the basis of SNPs in linkage disequilibrium is available at GitHub (https://github.com/baillielab/GenOMICC_GWAS).Acknowledgements: We thank the members of the Banco Nacional de ADN and the GRA@CE cohort group; and the research participants and employees of 23andMe for making this work possible. A full list of contributors who have provided data that were collated in the HGI project, including previous iterations, is available online (https://www.covid19hg.org/acknowledgements).Change history: 11 July 2023: A Correction to this paper has been published at: https://doi.org/10.1038/s41586-023-06383-z. -- In the version of this article initially published, the name of Ana Margarita Baldión-Elorza, of the SCOURGE Consortium, appeared incorrectly (as Ana María Baldion) and has now been amended in the HTML and PDF versions of the article.Copyright © The Author(s) 2023, Critical illness in COVID-19 is an extreme and clinically homogeneous disease phenotype that we have previously shown1 to be highly efficient for discovery of genetic associations2. Despite the advanced stage of illness at presentation, we have shown that host genetics in patients who are critically ill with COVID-19 can identify immunomodulatory therapies with strong beneficial effects in this group3. Here we analyse 24,202 cases of COVID-19 with critical illness comprising a combination of microarray genotype and whole-genome sequencing data from cases of critical illness in the international GenOMICC (11,440 cases) study, combined with other studies recruiting hospitalized patients with a strong focus on severe and critical disease: ISARIC4C (676 cases) and the SCOURGE consortium (5,934 cases). To put these results in the context of existing work, we conduct a meta-analysis of the new GenOMICC genome-wide association study (GWAS) results with previously published data. We find 49 genome-wide significant associations, of which 16 have not been reported previously. To investigate the therapeutic implications of these findings, we infer the structural consequences of protein-coding variants, and combine our GWAS results with gene expression data using a monocyte transcriptome-wide association study (TWAS) model, as well as gene and protein expression using Mendelian randomization. We identify potentially druggable targets in multiple systems, including inflammatory signalling (JAK1), monocyte–macrophage activation and endothelial permeability (PDE4A), immunometabolism (SLC2A5 and AK5), and host factors required for viral entry and replication (TMPRSS2 and RAB2A).GenOMICC was funded by Sepsis Research (the Fiona Elizabeth Agnew Trust), the Intensive Care Society, a Wellcome Trust Senior Research Fellowship (to J.K.B., 223164/Z/21/Z), the Department of Health and Social Care (DHSC), Illumina, LifeArc, the Medical Research Council, UKRI, a BBSRC Institute Program Support Grant to the Roslin Institute (BBS/E/D/20002172, BBS/E/D/10002070 and BBS/E/D/30002275) and UKRI grants MC_PC_20004, MC_PC_19025, MC_PC_1905 and MRNO2995X/1. A.D.B. acknowledges funding from the Wellcome PhD training fellowship for clinicians (204979/Z/16/Z), the Edinburgh Clinical Academic Track (ECAT) programme. This research is supported in part by the Data and Connectivity National Core Study, led by Health Data Research UK in partnership with the Office for National Statistics and funded by UK Research and Innovation (grant MC_PC_20029). Laboratory work was funded by a Wellcome Intermediate Clinical Fellowship to B.F. (201488/Z/16/Z). We acknowledge the staff at NHS Digital, Public Health England and the Intensive Care National Audit and Research Centre who provided clinical data on the participants; and the National Institute for Healthcare Research Clinical Research Network (NIHR CRN) and the Chief Scientist’s Office (Scotland), who facilitate recruitment into research studies in NHS hospitals, and to the global ISARIC and InFACT consortia. GenOMICC genotype controls were obtained using UK Biobank Resource under project 788 funded by Roslin Institute Strategic Programme Grants from the BBSRC (BBS/E/D/10002070 and BBS/E/D/30002275) and Health Data Research UK (HDR-9004 and HDR-9003). UK Biobank data were used in the GSMR analyses presented here under project 66982. The UK Biobank was established by the Wellcome Trust medical charity, Medical Research Council, Department of Health, Scottish Government and the Northwest Regional Development Agency. It has also had funding from the Welsh Assembly Government, British Heart Foundation and Diabetes UK. The work of L.K. was supported by an RCUK Innovation Fellowship from the National Productivity Investment Fund (MR/R026408/1). J.Y. is supported by the Westlake Education Foundation. SCOURGE is funded by the Instituto de Salud Carlos III (COV20_00622 to A.C., PI20/00876 to C.F.), European Union (ERDF) ‘A way of making Europe’, Fundación Amancio Ortega, Banco de Santander (to A.C.), Cabildo Insular de Tenerife (CGIEU0000219140 ‘Apuestas científicas del ITER para colaborar en la lucha contra la COVID-19’ to C.F.) and Fundación Canaria Instituto de Investigación Sanitaria de Canarias (PIFIISC20/57 to C.F.). We also acknowledge the contribution of the Centro National de Genotipado (CEGEN) and Centro de Supercomputación de Galicia (CESGA) for funding this project by providing supercomputing infrastructures. A.D.L. is a recipient of fellowships from the National Council for Scientific and Technological Development (CNPq)-Brazil (309173/2019-1 and 201527/2020-0)
A second update on mapping the human genetic architecture of COVID-19
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- Sato T
- Sato Y
- Satterstrom FK
- Saunderson A
- Saunderson P
- Savage F
- Savage S
- Savill H
- Sayan A
- Scanlon J
- Scarpini E
- Schaefer B
- Schaefer M
- Scherer SW
- Scherewode J
- Schiabor Barrett KM
- Schmidt A
- Schmidt SV
- Schneider J
- Scholefield B
- Schommers P
- Schon K
- Schreiber S
- Schroeder P
- Schulte EC
- Schulte EC
- Schulze TG
- Schumacher N
- Schurmann C
- Schwinn M
- Scollo C
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- Scott RH
- Scott T
- Scott Z
- Scriven J
- Sealock JM
- Seaman B
- Sedaghati-khayat B
- Seed C
- Segura T
- Segura-Kato Y
- Segura-Kato Y
- Sekikawa Y
- Sell C
- Sellick K
- Selvanayagam S
- Semple G
- Semple MG
- Senaratne D
- Senner F
- Sequeros CB
- Serbanescu MA
- Serna-Muñoz R
- Serra-Llovich A
- Serrano-Heras G
- Serrano-Ruiz A
- Service J
- Shafique H
- Shah MR
- Shah N
- Shah PK
- Shaheen D
- Shahin D
- Shahin MA
- Shaikh F
- Shamah-Levy T
- Shankar-Hari M
- Shanmugasundaram P
- Sharland E
- Shastri AJ
- Shaw D
- Shaw DM
- Shaw J
- Shaw L
- Shaw R
- Shelley B
- Shelton JF
- Shelton S
- Shen X
- Shepardson S
- Shepherd A
- Shepperson A
- Shibata Y
- Shibusawa T
- Shiel J
- Shiel R
- Shimada H
- Shimada T
- Shimizu T
- Shin E
- Shinoki M
- Shiomi T
- Ship L
- Shirai Y
- Shiroyama T
- Shivanathan I
- Shokkar R
- Shoko T
- Shoma A
- Shoremekun A
- Short A
- Short S
- Shorter S
- Shortt J
- Shovelton C
- Shuey MM
- Shuker K
- Sibbett L
- Sicat C
- Sidall E
- Siddiq A
- Sierra-Vargas MP
- Sifuentes-Osornio J
- Silbiger VN
- Silva AX
- Silva P
- Sim M
- Simms R
- Simpson J
- Simpson K
- Simpson S
- Sims T
- Sin DD
- Sinclair S
- Sinfield E
- Singh I
- Singh J
- Singler K
- Singleton J
- Sipeky C
- Sirui Z
- Sitonik M
- Skinner D
- Skogen V
- Skurk C
- Skyes D
- Slack L
- Slater V
- Slaughter M
- Slawson N
- Slevin K
- Sloan B
- Sloane G
- Smagulova Z
- Smalira A
- Smallwood A
- Smeaton J
- Smedley C
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- Smith R
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- Smith T
- Smithson E
- Smits G
- Smoller JW
- Smuts S
- Smyth D
- Smythe M
- Sobh A
- Soler-Palacin P
- Solier A
- Sollesta K
- Solligård E
- Solomonson M
- Solomonson M
- Sonehara K
- Sonobe K
- Soria JM
- Soriano A
- Souto JC
- Speight A
- Speirs S
- Spencer CCA
- Spencer K
- Spencer S
- Spinner CD
- Spivey M
- Springle P
- Sra S
- Sri-Chandana C
- Srikaran S
- St-Cyr J
- Stacey A
- Stagg C
- Stammers K
- Stapleton L
- Stark KJ
- Stead R
- Stefansson K
- Stefánsson H
- Stenhouse A
- Stephens D
- Stephenson E
- Stephenson L
- Stern S
- Stetsenko I
- Stevens C
- Stevenson L
- Stewart K
- Stewart R
- Stickley J
- Stoddard E
- Stoddart E
- Stojak J
- Stone S
- Stones E
- Stowe B
- Strachan D
- Striano P
- Stroud K
- Stroud N
- Strug LJ
- Stuart C
- Stuckey A
- Suarez JC
- Subramanian D
- Subramanian G
- Sucheston-Campbell L
- Sugiura H
- Sugiyama M
- Sukha A
- Sukhatme MG
- Sukumaran A
- Summers C
- Summers J
- Sumoy L
- Sumoy L
- Sun L
- Sundaram R
- Sutherland I
- Sutherland S-B
- Suwalski P
- Suzuki K
- Suzuki S
- Suzuki Y
- Swain A
- Sweeney L
- Sweet K
- Swets M
- Swinger R
- Symon L
- Symons A
- Sypniewski M
- Szabo D
- Szakmany T
- Szentpéteri JL
- Szoor-McElhinney H
- Sztromwasser P
- Szymiczek K
- Sánchez FG
- Sækmose SG
- Sørensen E
- T-Michael H
- Tagaya E
- Tagliavini E
- Taher A
- Taher J
- Takada M
- Takagi H
- Takahashi K
- Takahashi K
- Takahashi K
- Takahashi M
- Takahashi M
- Takahashi T
- Takaku Y
- Takano K
- Takata T
- Takayanagi N
- Takeda Y
- Takeuchi M
- Taki R
- Tamayo E
- Tamayo-Velasco A
- Tampsett R
- Tanaka A
- Tanaka H
- Tanate A
- Tanck A
- Taneski F
- Tani M
- Tanigawa Y
- Tanino Y
- Taniyama D
- Tanudjaja F
- Taracido-Fernandez JC
- Tardif N
- Tariq A
- Tateishi T
- Tateno H
- Tatham K
- Tauekelova A
- Tauro S
- Tavares S
- Taylor B
- Taylor C
- Taylor J
- Taylor J-A
- Taylor K
- Taylor M
- Taylor M
- Tebbutt J
- Tedstone R
- Teles A
- Templeton M
- Tench H
- Tenesa A
- Tenorio-Castaño JA
- Tentorio P
- Teoh PC
- Teper A
- Terai H
- Terranova L
- Tetla D
- Teumer A
- Texeira J
- Thanasi M
- Thani AA
- Thankachen M
- Thibeault C
- Thirlwall Y
- Thirumaran M
- Thiruvahindrapuram B
- Thomas A
- Thomas A
- Thomas A
- Thomas B
- Thomas E
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- Thomas J
- Thomas K
- Thomas M
- Thomas R
- Thomas V
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- Thompson G
- Thompson M
- Thompson R
- Thompson WK
- Thomson N
- Thornton D
- Thornton L
- Thorpe C
- Thrasyvoulou L
- Thrush J
- Thwaites V
- Tibke C
- Tiembe N
- Tierney C
- Tilbey S
- Tiller H
- Tilney E
- Timens W
- Timlick E
- Timpson NJ
- Ting L
- Tiongson G
- Tivenan H
- Toapanta D
- Tobar-Calfucoy EA
- Todd A
- Todd L
- Togashi Y
- Toghill H
- Tohda S
- Tokunaga K
- Tolson M
- Tomas AL
- Tomasi M
- Tomkova G
- Tomlinson J
- Tomono K
- Tonby K
- Tonks L
- Toohie J
- Torky MS
- Torrents D
- Torres-Espíndola LM
- Torres-Tobar L
- Toxqui-Merchant LE
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- Treus E
- Tridente A
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- Trumper E
- Tse SM
- Tsechoeva T
- Tselios C
- Tsilidis K
- Tsinaslanidis G
- Tsourlos S
- Tsuchida T
- Tsuo K
- Tubiana S
- Tucci A
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- Tuckey V
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- Tully R
- Turebayeva G
- Turki S
- Turley C
- Turley P
- Turnbull A
- Turner L
- Turner P
- Turner V
- Turner-Bone I
- Turney S
- Turtle L
- Turvey SE
- Tusié-Luna T
- Tutt G
- Tutton R
- Twiss S
- Tyl D
- Tyler A
- Tzoulaki I
- Téllez L
- Uchimura Y
- Ueda S
- Ueda T
- Uellendahl-Werth F
- Uitterlinden AG
- Ullum H
- Umeda A
- Upadhyay KJ
- Upton J
- Urioste M
- Urrechaga E
- Usher M
- Utsugi M
- Uwamino Y
- Vadgama N
- Vadla MS
- Vaida M
- Valdeavella K
- Valdés PA
- Valencia-Ramos J
- Valenti L
- Valenzuela-Jorquera H
- Vallerga CL
- Valsecchi MG
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- Van der Laan S
- Van Heel DA
- Van Heel DA
- Van Koutrick L
- Vandernoot I
- Varghese M
- Vasilevska-Ristovska J
- Vassell K
- Vedage D
- Veerapen K
- Vega J
- Vehreschild MJGT
- Velasco DG
- Velázquez-Cruz R
- Venkatesh H
- Verdugo RA
- Verdugo RA
- Vergasova E
- Verlander M
- Vertue M
- Verula J
- Vigueras-Hernández A
- Vigurs C
- Villa A
- Villalonga JM
- Vincent R
- Virgilio E
- Virginia M-RA
- Vitart V
- Vizcaychipi M
- Vlasschaert C
- Vochin A
- Volland S
- Von Hohenstaufen Puoti KA
- Voza A
- Vuylsteke A
- Várnai R
- Vázquez-Pérez JA
- Wacker EM
- Wackett T
- Wadams B
- Waddell G
- Waddington N
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- Wagstaff V
- Waite AAC
- Wakabayashi A
- Wakahara K
- Wakefield P
- Wakinshaw F
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- Walker C
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- Wang X
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- Washington NL
- Wassall H
- Wasson C
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- Watanabe K
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- Welters I
- Wendorff M
- Wendtner CM
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- Whitton C
- Whyte C
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- Wiegrebe S
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- Wilkinson B
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- Witzke O
- Wolf-Roberts R
- Wolford BN
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- Woolcock M
- Woolley AE
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- Worsley L
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- Wu Y
- Wulandari R
- Wylie K
- Wyllie DH
- Wynter I
- Xavier K
- Xue X
- Yagi K
- Yamada M
- Yamada Y
- Yamagata K
- Yamasaki M
- Yang J
- Yaspan B
- Yassen AM
- Yasui Y
- Yates B
- Yatomi M
- Ye C
- Yermakovich D
- Yeung RSM
- Yi X
- Yonekawa A
- Yoo S
- Yoon K
- Yoshida K
- Yoshida S
- Yoshida S
- Yoshida T
- Yoshihara T
- Yoshiya K
- Yoshiyama T
- Young M
- Yue F
- Yun N
- Yáñez CE
- Yáñez Z
- Zainulabid UA
- Zainy T
- Zak A
- Zaki A
- Zamikula J
- Zamudio IPM
- Zanella A
- Zapata-Contreras D
- Zapatamartinez M
- Zarate R
- Zarei N
- Zavaleta DAF
- Zawadzki P
- Zawati MH
- Zborowski AC
- Zeberg H
- Zechner M
- Zhang Q
- Zhao X
- Zheng C
- Zheng T
- Zhlawi HJ
- Zhlawi MWJ
- Zholdybayeva E
- Zhou W
- Zhu W
- Zitter L
- Zoller H
- Zongo O
- Zorloni C
- Zuñiga-Pacheco P
- Zárate RN
- Zúñiga-Ramos J
- Álvarez BG
- Ávila-Arcos MA
- Ávila-Arcos MC
- Özer O
- Überla K
- Þorsteinsdóttir U
- Publication venue
- Nature Research
- Publication date
- 21/06/2023
- Field of study