Search Results - "Common variants"

Unraveling genetic risk contributions to nonverbal status in autism spectrum disorder probands

Huan Liu, Shenghan Wang, Binbin Cao, Jijun Zhu, Zhifang Huang, Pan Li, Shunjie Zhang, Xian Liu, Jing Yu, Zhongting Huang, Linzhuo Lv, Fuqiang Cai, Weixin Liu, Zhijian Song, Yuxin Liu, Tao Pang, Suhua Chang, Ying Chen, Junfang Chen, Wen-Xiong Chen

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Polygenic score analysis identifies distinct genetic risk profiles in Alzheimer’s disease comorbidities

Carlos F. Hernández, Camilo Villaman, Costin Leu, Dennis Lal, Ignacio Mata, Andrés D. Klein, Eduardo Pérez-Palma

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Meta-Analysis of Common and Rare Variants

Michailidou, Kyriaki^Aff3

Evangelou, Evangelos^Aff2, Walker, John M.^Aff1

Polygenic prediction of human longevity on the supposition of pervasive pleiotropy

Jabalameli, M. Reza, Lin, Jhih-Rong, Zhang, Quanwei, Wang, Zhen, Mitra, Joydeep, Nguyen, Nha, Gao, Tina, Khusidman, Mark, Sathyan, Sanish, Atzmon, Gil^{Aff1, Aff2, Aff4}, Milman, Sofiya^{Aff1, Aff2}, Vijg, Jan, Barzilai, Nir^{Aff1, Aff2, Aff5}, Zhang, Zhengdong D.^{Aff1, IDs41598024690690_cor1}

Genome‐Wide Scan of Fifth Finger Clinodactyly

Myoung Keun Lee, Noah Herrick, Mary L. Marazita, John R. Shaffer, Seth M. Weinberg

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Genetic variation in patent foramen ovale: a case-control genome-wide association study

Bosi Dong, Yajiao Li, Fandi Ai, Jia Geng, Ting Tang, Wan Peng, Yusha Tang, Hui Wang, Zixuan Tian, Fengxiao Bu, Lei Chen

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Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants

Pei-Shan Wang, Xin-Xia Yang, Qiao Wei, Yong-Ting Lv, Zhi-Ying Wu, Hong-Fu Li

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Familial Screening for the Prevention of Rare Diseases: A Focus on Lipodystrophy in Southern Saudi Arabia

Abuzenadah, Adel^{Aff1, Aff8}, Alganmi, Nofe^{Aff1, Aff2}, AlQurashi, Raghad, Hawsa, Esraa, AlOtibi, Abdullah, Hummadi, Abdulrahman, Nahari, Ahmed Ali^{Aff4, Aff5}, AlZelaye, Somaya, Aljuhani, Nasser R., Al-Attas, Manal, Abusamra, Heba, Turkistany, Shereen, Karim, Sajjad^{Aff1, Aff8}, Mirza, Zeenat^{Aff8, Aff9}, Al-Qahtani, Mohammed^{Aff1, Aff8}, Chaudhary, Adeel^{Aff1, Aff10}, Al Eissa, Mariam M.^{Aff3, Aff11, IDs44197023001825_cor17}

Common genetic variants associated with risk of Parkinson’s disease in non-European populations: A PROSPERO registered systematic review based on genome-wide association studies

Claudino dos Santos, Júlio César ^{1, 2, 3, †}, Ribeiro Junior, Howard Lopes ^{1, 4, 5, ⁎, †}, Pires, Jackson Frederico ^{6, †}, Cabrera Mano, Gabriela Braga ^{7, †}, Esposito Dias, Fabricyo de Faria ⁵, Caetano Goes, João Vitor ^{1, 4}, Pinheiro Gusmão, Camilla Teixeira ¹, da Cunha Barreto-Vianna, André Rodrigues ⁸, Filippi Carlo, Ettore José ⁹, de Lucena Viana, Tayenne Nélly ¹⁰, de Almeida Lins, Camila ¹¹, Ferreira Maciel Gusmão, Jonas Nogueira ⁴, de Carvalho Leitão, Renata Ferreira ²

Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants

Qiao, Lu ^{1, 2}, Welch, Carrie L. ¹, Hernan, Rebecca ³, Wynn, Julia ¹, Krishnan, Usha S. ¹, Zalieckas, Jill M. ^{4, 5}, Buchmiller, Terry ⁴, Khlevner, Julie ¹, De, Aliva ¹, Farkouh-Karoleski, Christiana ¹, Wagner, Amy J. ⁶, Heydweiller, Andreas ⁷, Mueller, Andreas C. ⁸, de Klein, Annelies ⁹, Warner, Brad W. ¹⁰, Maj, Carlo ^{11, 37}, Chung, Dai ¹², McCulley, David J. ¹³, Schindel, David ¹⁴, Potoka, Douglas ¹⁵, Fialkowski, Elizabeth ¹⁶, Schulz, Felicitas ¹⁷, Kipfmuller, Florian ⁸, Lim, Foong-Yen ¹⁸, Magielsen, Frank ⁹, Mychaliska, George B. ¹⁹, Aspelund, Gudrun ¹, Reutter, Heiko Martin ²⁰, Needelman, Howard ²¹, Schnater, J. Marco ²², Fisher, Jason C. ²³, Azarow, Kenneth ¹⁶, Elfiky, Mahmoud ²⁴, Nöthen, Markus M. ²⁵, Danko, Melissa E. ¹², Li, Mindy ²⁶, Kosiński, Przemyslaw ²⁷, Wijnen, Rene M.H. ²², Cusick, Robert A. ²¹, Soffer, Samuel Z. ²⁸, Cochius-Den Otter, Suzan C.M. ²⁹, Schaible, Thomas ³⁰, Crombleholme, Timothy ¹⁴, Duron, Vincent P. ³¹, Donahoe, Patricia K. ^{32, 33}, Sun, Xin ¹³, High, Frances A. ^{4, 32, 34}, Bendixen, Charlotte ⁷, Brosens, Erwin ⁹, Shen, Yufeng ^{2, 35, 36, ∗}, Chung, Wendy K. ^{1, 3, ∗∗}

Detecting Rare Variants

Feng, Tao^Aff1_24, Zhu, Xiaofeng^Aff1_24

Elston, Robert C.^AffID1, Satagopan, Jaya M.^AffID2, Sun, Shuying^AffID3

Scent of COVID-19: Whole-Genome Sequencing Analysis Reveals the Role of ACE2, IFI44, and NDUFAF4 in Long-Lasting Olfactory Dysfunction

Beatrice Spedicati, Alessandro Pecori, Maria Pina Concas, Aurora Santin, Romina Ruberto, Giuseppe Giovanni Nardone, Andrea D’Alessandro, Giancarlo Tirelli, Paolo Boscolo-Rizzo, Giorgia Girotto

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Association of common genetic variants with chronic axonal polyneuropathy in the general population: a genome-wide association study

Noor E. Taams, Maria J. Knol, Rens Hanewinckel, Judith Drenthen, Mary M. Reilly, Pieter A. van Doorn, Hieab H. H. Adams, M. Arfan Ikram

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About the Genetic Contribution to Chronic Dizziness and Episodic Vertigo

Lopez-Escamez, Jose A.^{Aff1, Aff2, Aff3, Aff4, IDs10162023009212_cor1}

In silico prioritisation of microRNA-associated common variants in multiple sclerosis

Fashina, Ifeolutembi A.^{Aff1, Aff2, Aff3}, McCoy, Claire E., Furney, Simon J.^{Aff4, IDs40246023004784_cor3}

Genetics of Childhood-onset Schizophrenia 2019 Update

Forsyth, Jennifer K, Asarnow, Robert F

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A general statistic to test an optimally weighted combination of common and/or rare variants.

Zhang, Jianjun, Wu, Baolin, Sha, Qiuying, Zhang, Shuanglin, Wang, Xuexia

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Pathogenesis of Endometriosis: Genetics

Rahmioglu, Nilufer^{Aff2, Aff3}, Zondervan, Krina T.^{Aff2, Aff3}

Oral, Engin, editor^Aff1

A relatively common hypomorphic variant in WARS2 causes monogenic disease

Ilinca, Andreea, Kafantari, Efthymia, Puschmann, Andreas

Genome‐wide meta‐analyses identify five new risk loci for nonsyndromic orofacial clefts in the Chinese Han population

Yafen Yu, Qi Zhen, Weiwei Chen, Yanqin Yu, Zhuo Li, Yirui Wang, Wencheng Fan, Sihan Luo, Daiyue Wang, Yuanming Bai, Zhuan Bian, Miao He, Liangdan Sun

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