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2010, 2nd ed., ISBN 9780195398441, xxiii, 676
With contributions from leaders in the field from around the world, this new edition of Human Genome Epidemiology is a fully updated look at the ways in which... 
epidemiology | Genetic Predisposition to Disease | Genetics, Medical | Genetic disorders | Methodology | Genomics | methods | Medical genetics | Genetic Diseases, Inborn | Genetic Screening | Genome, Human | Epidemiology
Book
Circulation, ISSN 0009-7322, 08/2012, Volume 126, Issue 9, pp. 1143 - 1172
Background-The goal of this statement was to review the available literature on surveillance, screening, evaluation, and management strategies and put forward... 
Cardiopulmonary bypass | Pediatrics | Heart diseases, follow-up studies, brain | AHA Scientific Statements | Heart defects, congenital | VENTRICULAR SEPTAL-DEFECT | CARDIAC & CARDIOVASCULAR SYSTEMS | APOLIPOPROTEIN-E GENOTYPE | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | SCHOOL-AGED CHILDREN | heart diseases, follow-up studies, brain | pediatrics | HYPOTHERMIC CIRCULATORY ARREST | cardiopulmonary bypass | heart defects, congenital | PERIPHERAL VASCULAR DISEASE | CORRECTIVE CARDIAC-SURGERY | QUALITY-OF-LIFE | CEREBRAL-BLOOD-FLOW | EXTRACORPOREAL MEMBRANE-OXYGENATION | HEALTH-STATUS | Neuroimaging | Postoperative Complications - etiology | Brain Damage, Chronic - diagnosis | Prevalence | Heart Defects, Congenital - surgery | Humans | Postoperative Complications - prevention & control | Developmental Disabilities - prevention & control | Genetic Diseases, Inborn - epidemiology | Learning Disorders - etiology | Cardiac Surgical Procedures | Learning Disorders - therapy | Learning Disorders - epidemiology | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Intellectual Disability - epidemiology | Comorbidity | Learning Disorders - diagnosis | Developmental Disabilities - etiology | Risk Factors | Postoperative Complications - therapy | Postoperative Complications - epidemiology | Developmental Disabilities - therapy | Intellectual Disability - therapy | Developmental Disabilities - epidemiology | Brain Damage, Chronic - etiology | Algorithms | Heart Defects, Congenital - complications | House Calls | Neurologic Examination | Aftercare | Intellectual Disability - diagnosis | Adolescent | Quality of Life | Brain Damage, Chronic - epidemiology | Disease Management | Heart Defects, Congenital - therapy | Intellectual Disability - etiology | Early Diagnosis | Brain Damage, Chronic - prevention & control | Coronary artery bypass | Demographic aspects | Patient outcomes | Child development deviations | Reports | Congenital heart disease | Research | Risk factors | Developmental disabilities
Journal Article
Lancet Psychiatry, The, ISSN 2215-0366, 2015, Volume 2, Issue 10, pp. 909 - 916
Summary Background Autism spectrum disorder (ASD) phenomenology is reported to be more common in individuals with some genetic syndromes than in the general... 
Psychiatry | PSYCHIATRY | LANGE | CORNELIA | Prevalence | Autism Spectrum Disorder - epidemiology | Humans | Genetic Diseases, Inborn - complications | Female | Male | Risk | Genetic Diseases, Inborn - epidemiology | Autism Spectrum Disorder - etiology | Genetic Diseases, Inborn - diagnosis | Autism Spectrum Disorder - diagnosis
Journal Article
by Monies, Dorota and Abouelhoda, Mohamed and AlSayed, Moeenaldeen and Alhassnan, Zuhair and Alotaibi, Maha and Kayyali, Husam and Al-Owain, Mohammed and Shah, Ayaz and Rahbeeni, Zuhair and Al-Muhaizea, Mohammad A and Alzaidan, Hamad I and Cupler, Edward and Bohlega, Saeed and Faqeih, Eissa and Faden, Maha and Alyounes, Banan and Jaroudi, Dyala and Goljan, Ewa and Elbardisy, Hadeel and Akilan, Asma and Albar, Renad and Aldhalaan, Hesham and Gulab, Shamshad and Chedrawi, Aziza and Al Saud, Bandar K and Kurdi, Wesam and Makhseed, Nawal and Alqasim, Tahani and El Khashab, Heba Y and Al-Mousa, Hamoud and Alhashem, Amal and Kanaan, Imaduddin and Algoufi, Talal and Alsaleem, Khalid and Basha, Talal A and Al-Murshedi, Fathiya and Khan, Sameena and Al-Kindy, Adila and Alnemer, Maha and Al-Hajjar, Sami and Alyamani, Suad and Aldhekri, Hasan and Al-Mehaidib, Ali and Arnaout, Rand and Dabbagh, Omar and Shagrani, Mohammad and Broering, Dieter and Tulbah, Maha and Alqassmi, Amal and Almugbel, Maisoon and AlQuaiz, Mohammed and Alsaman, Abdulaziz and Al-Thihli, Khalid and Sulaiman, Raashda A and Al-Dekhail, Wajeeh and Alsaegh, Abeer and Bashiri, Fahad A and Qari, Alya and Alhomadi, Suzan and Alkuraya, Hisham and Alsebayel, Mohammed and Hamad, Muddathir H and Szonyi, Laszlo and Abaalkhail, Faisal and Al-Mayouf, Sulaiman M and Almojalli, Hamad and Alqadi, Khalid S and Elsiesy, Hussien and Shuaib, Taghreed M and Seidahmed, Mohammed Zain and Abosoudah, Ibraheem and Akleh, Hana and AlGhonaium, Abdulaziz and Alkharfy, Turki M and Al Mutairi, Fuad and Eyaid, Wafa and Alshanbary, Abdullah and Sheikh, Farrukh R and Alsohaibani, Fahad I and Alsonbul, Abdullah and Al Tala, Saeed and Balkhy, Soher and Bassiouni, Randa and Alenizi, Ahmed S and Hussein, Maged H and Hassan, Saeed and Khalil, Mohamed and Tabarki, Brahim and Alshahwan, Saad and Oshi, Amira and Sabr, Yasser and Alsaadoun, Saad and Salih, Mustafa A and Mohamed, Sarar and Sultana, Habiba and Tamim, Abdullah and El-Haj, Moayad and Alshahrani, Saif and Bubshait, Dalal K and Alfadhel, Majid and ...
Human Genetics, ISSN 0340-6717, 8/2017, Volume 136, Issue 8, pp. 921 - 939
Journal Article