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  1. 12321
    “…RESULTS: HRS and HC subjects did not significantly differ in age (t=0.68, p=0.497) and sex (X2=0.003, p=0.958). Intellectual quotient was higher in HC (mean=105.4 ± 11.28) than in HRS subjects (98.63 ± 14.27, t=2.53, p=0.013). …”
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    F29. HIGH-RISK SYMPTOMS FOR PSYCHOSIS IN ADOLESCENTS AND ITS RELATIONSHIP WITH FAMILY BURDEN
  2. 12322
    por Mannucci, Ilaria, Dang, Nghi D. P., Huber, Hannes, Murry, Jaclyn B., Abramson, Jeff, Althoff, Thorsten, Banka, Siddharth, Baynam, Gareth, Bearden, David, Beleza-Meireles, Ana, Benke, Paul J., Berland, Siren, Bierhals, Tatjana, Bilan, Frederic, Bindoff, Laurence A., Braathen, Geir Julius, Busk, Øyvind L., Chenbhanich, Jirat, Denecke, Jonas, Escobar, Luis F., Estes, Caroline, Fleischer, Julie, Groepper, Daniel, Haaxma, Charlotte A., Hempel, Maja, Holler-Managan, Yolanda, Houge, Gunnar, Jackson, Adam, Kellogg, Laura, Keren, Boris, Kiraly-Borri, Catherine, Kraus, Cornelia, Kubisch, Christian, Le Guyader, Gwenael, Ljungblad, Ulf W., Brenman, Leslie Manace, Martinez-Agosto, Julian A., Might, Matthew, Miller, David T., Minks, Kelly Q., Moghaddam, Billur, Nava, Caroline, Nelson, Stanley F., Parant, John M., Prescott, Trine, Rajabi, Farrah, Randrianaivo, Hanitra, Reiter, Simone F., Schuurs-Hoeijmakers, Janneke, Shieh, Perry B., Slavotinek, Anne, Smithson, Sarah, Stegmann, Alexander P. A., Tomczak, Kinga, Tveten, Kristian, Wang, Jun, Whitlock, Jordan H., Zweier, Christiane, McWalter, Kirsty, Juusola, Jane, Quintero-Rivera, Fabiola, Fischer, Utz, Yeo, Nan Cher, Kreienkamp, Hans-Jürgen, Lessel, Davor
    Publicado 2021
    “…All 19 individuals harboring heterozygous missense variants within helicase core motifs (HCMs) have global developmental delay, intellectual disability, severe speech impairment, and gait abnormalities. …”
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    Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders
  3. 12323
    “…The higher proportion of Black children compared with White and Hispanic children classified as having intellectual disability was consistent with previous findings. …”
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    Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2018
  4. 12324
    por Castelpietra, Giulio, Knudsen, Ann Kristin Skrindo, Agardh, Emilie E., Armocida, Benedetta, Beghi, Massimiliano, Iburg, Kim Moesgaard, Logroscino, Giancarlo, Ma, Rui, Starace, Fabrizio, Steel, Nicholas, Addolorato, Giovanni, Andrei, Catalina Liliana, Andrei, Tudorel, Ayuso-Mateos, Jose L, Banach, Maciej, Bärnighausen, Till Winfried, Barone-Adesi, Francesco, Bhagavathula, Akshaya Srikanth, Carvalho, Felix, Carvalho, Márcia, Chandan, Joht Singh, Chattu, Vijay Kumar, Couto, Rosa A.S., Cruz-Martins, Natália, Dargan, Paul I., Deuba, Keshab, da Silva, Diana Dias, Fagbamigbe, Adeniyi Francis, Fernandes, Eduarda, Ferrara, Pietro, Fischer, Florian, Gaal, Peter Andras, Gialluisi, Alessandro, Haagsma, Juanita A., Haro, Josep Maria, Hasan, M. Tasdik, Hasan, Syed Shahzad, Hostiuc, Sorin, Iacoviello, Licia, Iavicoli, Ivo, Jamshidi, Elham, Jonas, Jost B., Joo, Tamas, Jozwiak, Jacek Jerzy, Katikireddi, Srinivasa Vittal, Kauppila, Joonas H., Khan, Moien A.B., Kisa, Adnan, Kisa, Sezer, Kivimäki, Mika, Koly, Kamrun Nahar, Koyanagi, Ai, Kumar, Manasi, Lallukka, Tea, Langguth, Berthold, Ledda, Caterina, Lee, Paul H., Lega, Ilaria, Linehan, Christine, Loureiro, Joana A., Madureira-Carvalho, Áurea M, Martinez-Raga, Jose, Mathur, Manu Raj, McGrath, John J., Mechili, Enkeleint A., Mentis, Alexios-Fotios A., Mestrovic, Tomislav, Miazgowski, Bartosz, Mirica, Andreea, Mirijello, Antonio, Moazen, Babak, Mohammed, Shafiu, Mulita, Francesk, Nagel, Gabriele, Negoi, Ionut, Negoi, Ruxandra Irina, Nwatah, Vincent Ebuka, Padron-Monedero, Alicia, Panda-Jonas, Songhomitra, Pardhan, Shahina, Pasovic, Maja, Patel, Jay, Petcu, Ionela-Roxana, Pinheiro, Marina, Pollok, Richard Charles G., Postma, Maarten J., Rawaf, David Laith, Rawaf, Salman, Romero-Rodríguez, Esperanza, Ronfani, Luca, Sagoe, Dominic, Sanmarchi, Francesco, Schaub, Michael P, Sharew, Nigussie Tadesse, Shiri, Rahman, Shokraneh, Farhad, Sigfusdottir, Inga Dora, Silva, João Pedro, Silva, Renata, Socea, Bogdan, Szócska, Miklós, Tabarés-Seisdedos, Rafael, Torrado, Marco, Tovani-Palone, Marcos Roberto, Vasankari, Tommi Juhani, Veroux, Massimiliano, Viner, Russell M., Werdecker, Andrea, Winkler, Andrea Sylvia, Hay, Simon I., Ferrari, Alize J., Naghavi, Mohsen, Allebeck, Peter, Monasta, Lorenzo
    Publicado 2022
    “…Over the 30 years studied, YLDs increased in eating disorders (14·9%;9·4-20·1) and drug use disorders (16·9%;8·9-26·3), and decreased in idiopathic developmental intellectual disability (–29·1%;23·8-38·5). YLLs decreased in self-harm (–27·9%;38·3-18·7). …”
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    The burden of mental disorders, substance use disorders and self-harm among young people in Europe, 1990–2019: Findings from the Global Burden of Disease Study 2019
  5. 12325
    “…Two authors (BAL, SLY) have licensed intellectual property for the detection of endometriosis. …”
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    Unexplained recurrent pregnancy loss and unexplained infertility: twins in disguise
  6. 12326
    por CERN. Geneva
    Publicado 2016
    “…</p> </li> <li> <p>INTEGRATION OF PEOPLE WITH INTELLECTUAL AND DEVELOPMENTAL DISABILITIES INTO SOCIETY<br /> How might we improve the cognitive development and communication skills, and consequently the quality of life, of people with IDD through ICT?…”
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    Challenge Based Innovation @ mediterranean - final presentations & prototype expo
  7. 12327
    “…Most focused on people with intellectual disabilities (n = 20) and psychosocial disabilities (n = 13). …”
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    Effectiveness of interventions for improving social inclusion outcomes for people with disabilities in low‐ and middle‐income countries: A systematic review
  8. 12328
    “…The most common clinical symptoms were developmental delay, intellectual disability, and movement disorders. Behavioural problems were more common in L2HGA than in GA-I patients. …”
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    Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey
  9. 12329
    por Saffari, Afshin, Lau, Tracy, Tajsharghi, Homa, Karimiani, Ehsan Ghayoor, Kariminejad, Ariana, Efthymiou, Stephanie, Zifarelli, Giovanni, Sultan, Tipu, Toosi, Mehran Beiraghi, Sedighzadeh, Sahar, Siu, Victoria Mok, Ortigoza-Escobar, Juan Darío, AlShamsi, Aisha M, Ibrahim, Shahnaz, Al-Sannaa, Nouriya Abbas, Al-Hertani, Walla, Sandra, Whalen, Tarnopolsky, Mark, Alavi, Shahryar, Li, Chumei, Day-Salvatore, Debra-Lynn, Martínez-González, Maria Jesús, Levandoski, Kristin M, Bedoukian, Emma, Madan-Khetarpal, Suneeta, Idleburg, Michaela J, Menezes, Minal Juliet, Siddharth, Aishwarya, Platzer, Konrad, Oppermann, Henry, Smitka, Martin, Collins, Felicity, Lek, Monkol, Shahrooei, Mohmmad, Ghavideldarestani, Maryam, Herman, Isabella, Rendu, John, Faure, Julien, Baker, Janice, Bhambhani, Vikas, Calderwood, Laurel, Akhondian, Javad, Imannezhad, Shima, Mirzadeh, Hanieh Sadat, Hashemi, Narges, Doosti, Mohammad, Safi, Mojtaba, Ahangari, Najmeh, Torbati, Paria Najarzadeh, Abedini, Soheila, Salpietro, Vincenzo, Gulec, Elif Yilmaz, Eshaghian, Safieh, Ghazavi, Mohammadreza, Pascher, Michael T, Vogel, Marina, Abicht, Angela, Moutton, Sébastien, Bruel, Ange-Line, Rieubland, Claudine, Gallati, Sabina, Strom, Tim M, Lochmüller, Hanns, Mohammadi, Mohammad Hasan, Alvi, Javeria Raza, Zackai, Elaine H, Keena, Beth A, Skraban, Cara M, Berger, Seth I, Andrew, Erin H, Rahimian, Elham, Morrow, Michelle M, Wentzensen, Ingrid M, Millan, Francisca, Henderson, Lindsay B, Dafsari, Hormos Salimi, Jungbluth, Heinz, Gomez-Ospina, Natalia, McRae, Anne, Peter, Merlene, Veltra, Danai, Marinakis, Nikolaos M, Sofocleous, Christalena, Ashrafzadeh, Farah, Pehlivan, Davut, Lemke, Johannes R, Melki, Judith, Benezit, Audrey, Bauer, Peter, Weis, Denisa, Lupski, James R, Senderek, Jan, Christodoulou, John, Chung, Wendy K, Goodchild, Rose, Offiah, Amaka C, Moreno-De-Luca, Andres, Suri, Mohnish, Ebrahimi-Fakhari, Darius, Houlden, Henry, Maroofian, Reza
    Publicado 2023
    “…Analysis of disease-associated manifestations delineated a phenotypic spectrum ranging from normal cognition and mild gait disturbance to congenital arthrogryposis, global developmental delay, intellectual disability, absent speech and inability to walk. …”
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    The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders
  10. 12330
    por Sønderby, Ida E., van der Meer, Dennis, Moreau, Clara, Kaufmann, Tobias, Walters, G. Bragi, Ellegaard, Maria, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Bøen, Rune, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Crespo-Facorro, Benedicto, Curran, Joanne E., Dale, Anders M., Dalvie, Shareefa, Dazzan, Paola, de Geus, Eco J. C., de Zubicaray, Greig I., de Zwarte, Sonja M. C., Desrivieres, Sylvane, Doherty, Joanne L., Donohoe, Gary, Draganski, Bogdan, Ehrlich, Stefan, Eising, Else, Espeseth, Thomas, Fejgin, Kim, Fisher, Simon E., Fladby, Tormod, Frei, Oleksandr, Frouin, Vincent, Fukunaga, Masaki, Gareau, Thomas, Ge, Tian, Glahn, David C., Grabe, Hans J., Groenewold, Nynke A., Gústafsson, Ómar, Haavik, Jan, Haberg, Asta K., Hall, Jeremy, Hashimoto, Ryota, Hehir-Kwa, Jayne Y., Hibar, Derrek P., Hillegers, Manon H. J., Hoffmann, Per, Holleran, Laurena, Holmes, Avram J., Homuth, Georg, Hottenga, Jouke-Jan, Hulshoff Pol, Hilleke E., Ikeda, Masashi, Jahanshad, Neda, Jockwitz, Christiane, Johansson, Stefan, Jönsson, Erik G., Jørgensen, Niklas R., Kikuchi, Masataka, Knowles, Emma E. M., Kumar, Kuldeep, Le Hellard, Stephanie, Leu, Costin, Linden, David E. J., Liu, Jingyu, Lundervold, Arvid, Lundervold, Astri Johansen, Maillard, Anne M., Martin, Nicholas G., Martin-Brevet, Sandra, Mather, Karen A., Mathias, Samuel R., McMahon, Katie L., McRae, Allan F., Medland, Sarah E., Meyer-Lindenberg, Andreas, Moberget, Torgeir, Modenato, Claudia, Sánchez, Jennifer Monereo, Morris, Derek W., Mühleisen, Thomas W., Murray, Robin M., Nielsen, Jacob, Nordvik, Jan E., Nyberg, Lars, Loohuis, Loes M. Olde, Ophoff, Roel A., Owen, Michael J., Paus, Tomas, Pausova, Zdenka, Peralta, Juan M., Pike, G. Bruce, Prieto, Carlos, Quinlan, Erin B., Reinbold, Céline S., Marques, Tiago Reis, Rucker, James J. H., Sachdev, Perminder S., Sando, Sigrid B., Schofield, Peter R., Schork, Andrew J., Schumann, Gunter, Shin, Jean, Shumskaya, Elena, Silva, Ana I., Sisodiya, Sanjay M., Steen, Vidar M., Stein, Dan J., Strike, Lachlan T., Suzuki, Ikuo K., Tamnes, Christian K., Teumer, Alexander, Thalamuthu, Anbupalam, Tordesillas-Gutiérrez, Diana, Uhlmann, Anne, Ulfarsson, Magnus O., van ‘t Ent, Dennis, van den Bree, Marianne B. M., Vanderhaeghen, Pierre, Vassos, Evangelos, Wen, Wei, Wittfeld, Katharina, Wright, Margaret J., Agartz, Ingrid, Djurovic, Srdjan, Westlye, Lars T., Stefansson, Hreinn, Stefansson, Kari, Jacquemont, Sébastien, Thompson, Paul M., Andreassen, Ole A.
    Publicado 2021
    “…Low-frequency 1q21.1 distal deletion and duplication copy number variant (CNV) carriers are predisposed to multiple neurodevelopmental disorders, including schizophrenia, autism and intellectual disability. Human carriers display a high prevalence of micro- and macrocephaly in deletion and duplication carriers, respectively. …”
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    1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans
  11. 12331
    “…This association was also observed for psychotic disorders (2·05 [1·37–3·06]; I(2)=80·81%), mood disorders (1·99 [1·46–2·71]; I(2)=68·32%), substance use disorders (1·76 [1·27–2·44]; I(2)=47·90%), and intellectual disabilities and developmental disorders (1·73 [1·29–2·31]; I(2)=90·15%) but not for anxiety disorders (1·07 [0·73–1·56]; I(2)=11·05%). …”
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    Mental disorders and risk of COVID-19-related mortality, hospitalisation, and intensive care unit admission: a systematic review and meta-analysis
  12. 12332
    por Zhang, Qi
    Publicado 2022
    “…Colleges and universities are the concentration of professional talents, with high intelligence, professional knowledge in business fields, and obvious talent and intellectual advantages. The university can organize experts and scholars to establish professional entrepreneurship guidance teams, give full play to the professional advantages of experts and scholars in their respective fields, carry out scientific research on entrepreneurship projects, guide students with entrepreneurial motivation to start businesses with professional standards, and promote scientific and technological innovation and technological entrepreneurship.…”
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    IDEOLOGY LED, PROCESS DRIVEN AND LAYERED PROMOTION — CONSTRUCTION OF INNOVATION AND ENTREPRENEURSHIP EDUCATION MODEL BASED ON EMOTIONAL BEHAVIOR CHANGE
  13. 12333
    por Zhao, Zhiguo, Huang, Fei
    Publicado 2022
    “…Colleges and universities are the concentration of professionals, with a high level of intelligence, professional knowledge in the business field, and obvious talent and intellectual advantages. The university can organize experts and scholars to establish a professional entrepreneurship guidance team, give full play to the professional advantages of experts and scholars in their respective fields, carry out scientific research on entrepreneurship projects, guide students with entrepreneurial motivation to start businesses according to professional standards, and promote scientific and technological innovation and scientific and technological entrepreneurship. …”
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    CONSTRUCTION AND PRACTICE OF INNOVATION AND ENTREPRENEURSHIP EDUCATION ECOSYSTEM IN LOCAL COLLEGES AND UNIVERSITIES FROM THE PERSPECTIVE OF EMOTION REGULATION -- A CASE STUDY OF HUAIYIN INSTITUTE OF TECHNOLOGY
  14. 12334
    Publicado 2009
    Tabla de Contenidos: “…Breaking through our own barriers / John Shepherd ; Becoming intellectually fearless / Anthony J. Palmer -- Pt. VI. …”
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    Libro
    Music education for changing times : guiding visions for practice /
  15. 12335
    por Monies, Dorota, Abouelhoda, Mohamed, AlSayed, Moeenaldeen, Alhassnan, Zuhair, Alotaibi, Maha, Kayyali, Husam, Al-Owain, Mohammed, Shah, Ayaz, Rahbeeni, Zuhair, Al-Muhaizea, Mohammad A., Alzaidan, Hamad I., Cupler, Edward, Bohlega, Saeed, Faqeih, Eissa, Faden, Maha, Alyounes, Banan, Jaroudi, Dyala, Goljan, Ewa, Elbardisy, Hadeel, Akilan, Asma, Albar, Renad, Aldhalaan, Hesham, Gulab, Shamshad, Chedrawi, Aziza, Al Saud, Bandar K, Kurdi, Wesam, Makhseed, Nawal, Alqasim, Tahani, El Khashab, Heba Y., Al-Mousa, Hamoud, Alhashem, Amal, Kanaan, Imaduddin, Algoufi, Talal, Alsaleem, Khalid, Basha, Talal A., Al-Murshedi, Fathiya, Khan, Sameena, Al-Kindy, Adila, Alnemer, Maha, Al-Hajjar, Sami, Alyamani, Suad, Aldhekri, Hasan, Al-Mehaidib, Ali, Arnaout, Rand, Dabbagh, Omar, Shagrani, Mohammad, Broering, Dieter, Tulbah, Maha, Alqassmi, Amal, Almugbel, Maisoon, AlQuaiz, Mohammed, Alsaman, Abdulaziz, Al-Thihli, Khalid, Sulaiman, Raashda A., Al-Dekhail, Wajeeh, Alsaegh, Abeer, Bashiri, Fahad A., Qari, Alya, Alhomadi, Suzan, Alkuraya, Hisham, Alsebayel, Mohammed, Hamad, Muddathir H, Szonyi, Laszlo, Abaalkhail, Faisal, Al-Mayouf, Sulaiman M., Almojalli, Hamad, Alqadi, Khalid S., Elsiesy, Hussien, Shuaib, Taghreed M., Seidahmed, Mohammed Zain, Abosoudah, Ibraheem, Akleh, Hana, AlGhonaium, Abdulaziz, Alkharfy, Turki M., Al Mutairi, Fuad, Eyaid, Wafa, Alshanbary, Abdullah, Sheikh, Farrukh R., Alsohaibani, Fahad I., Alsonbul, Abdullah, Al Tala, Saeed, Balkhy, Soher, Bassiouni, Randa, Alenizi, Ahmed S., Hussein, Maged H., Hassan, Saeed, Khalil, Mohamed, Tabarki, Brahim, Alshahwan, Saad, Oshi, Amira, Sabr, Yasser, Alsaadoun, Saad, Salih, Mustafa A., Mohamed, Sarar, Sultana, Habiba, Tamim, Abdullah, El-Haj, Moayad, Alshahrani, Saif, Bubshait, Dalal K., Alfadhel, Majid, Faquih, Tariq, El-Kalioby, Mohamed, Subhani, Shazia, Shah, Zeeshan, Moghrabi, Nabil, Meyer, Brian F., Alkuraya, Fowzan S.
    Publicado 2017
    “…Two of these genes were independently mutated in more than one family with similar phenotypes, which substantiates their link to human disease (AKAP6 in intellectual disability and UBR4 in early dementia). …”
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    The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
  16. 12336
    por Arora, Narendra K., Nair, M. K. C., Gulati, Sheffali, Deshmukh, Vaishali, Mohapatra, Archisman, Mishra, Devendra, Patel, Vikram, Pandey, Ravindra M., Das, Bhagabati C., Divan, Gauri, Murthy, G. V. S., Sharma, Thakur D., Sapra, Savita, Aneja, Satinder, Juneja, Monica, Reddy, Sunanda K., Suman, Praveen, Mukherjee, Sharmila B., Dasgupta, Rajib, Tudu, Poma, Das, Manoja K., Bhutani, Vinod K., Durkin, Maureen S., Pinto-Martin, Jennifer, Silberberg, Donald H., Sagar, Rajesh, Ahmed, Faruqueuddin, Babu, Nandita, Bavdekar, Sandeep, Chandra, Vijay, Chaudhuri, Zia, Dada, Tanuj, Dass, Rashna, Gourie-Devi, M., Remadevi, S., Gupta, Jagdish C., Handa, Kumud K., Kalra, Veena, Karande, Sunil, Konanki, Ramesh, Kulkarni, Madhuri, Kumar, Rashmi, Maria, Arti, Masoodi, Muneer A., Mehta, Manju, Mohanty, Santosh Kumar, Nair, Harikumaran, Natarajan, Poonam, Niswade, A. K., Prasad, Atul, Rai, Sanjay K., Russell, Paul S. S., Saxena, Rohit, Sharma, Shobha, Singh, Arun K., Singh, Gautam B., Sumaraj, Leena, Suresh, Saradha, Thakar, Alok, Parthasarathy, Sujatha, Vyas, Bhadresh, Panigrahi, Ansuman, Saroch, Munish K., Shukla, Rajan, Rao, K. V. Raghava, Silveira, Maria P., Singh, Samiksha, Vajaratkar, Vivek
    Publicado 2018
    “…All children were assessed for vision impairment (VI), epilepsy (Epi), neuromotor impairments including cerebral palsy (NMI-CP), hearing impairment (HI), speech and language disorders, autism spectrum disorders (ASDs), and intellectual disability (ID). Furthermore, 6–9-year-old children were also assessed for attention deficit hyperactivity disorder (ADHD) and learning disorders (LDs). …”
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    Neurodevelopmental disorders in children aged 2–9 years: Population-based burden estimates across five regions in India
  17. 12337
    por catherine, Auxilia, Anushya, Neelakandan
    Publicado 2022
    “…. — Further neuropsychological testing identified a global reduction in general intellectual function, with severe executive function deficits as well as poor verbal working — Neurology opinion obtained as a case of young onset FTD — MRI scan of the brain showed substantial bilateral, symmetrical frontal atrophy, with no evidence of white matter changes that would be typical of a vascular, vasculitic or inflammatory cause (figure 1). …”
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    A Case Report On Young Onset Frontal Temporal Dementia Presented As Catatonia
  18. 12338
    “…Give full play to the concentration of professionals, have a high degree of intelligence and professional knowledge in the business field, and have obvious talent and intellectual advantages. Experts and scholars can be organized to establish a professional bid winning guidance team, give full play to the business projects of experts and scholars in their respective fields, and carry out scientific research on entrepreneurial projects. …”
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    LAND CIRCULATION, FARMERS' WAGE LEVEL, LABOR FORCE CHARACTERISTICS AND THE BENEFITS OF AGRICULTURAL LAND SCALE MANAGEMENT: A STUDY ON THE CHANGES OF EMOTIONAL BEHAVIOR BASED ON THE SURVEY DATA OF JIANGXI PROVINCE
  19. 12339
    por Glinsky, Gennadi V.
    Publicado 2022
    “…Identification and characterization of 1944 genes comprising high-confidence down-steam regulatory targets of LTR7 and/or LTR5_Hs loci validated and extended these observations by documenting marked enrichments for genes implicated in neoplasm metastasis, intellectual disability, autism, multiple cancer types, Alzheimer’s, schizophrenia, and other brain disorders. …”
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    Molecular diversity and phenotypic pleiotropy of ancient genomic regulatory loci derived from human endogenous retrovirus type H (HERVH) promoter LTR7 and HERVK promoter LTR5_Hs and their contemporary impacts on pathophysiology of Modern Humans
  20. 12340
    “…SELECTION CRITERIA: We included randomized controlled trials (RCTs) and quasi‐RCTs comparing deworming drugs for soil‐transmitted helminths with placebo or no treatment in children aged 16 years or less, reporting on weight, haemoglobin, and formal tests of intellectual development. We also sought data on school attendance, school performance, and mortality. …”
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    Deworming drugs for soil‐transmitted intestinal worms in children: effects on nutritional indicators, haemoglobin, and school performance
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