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  1. Akula, Shyam K.; Chen, Allen Y.; Neil, Jennifer E.; Shao, Diane D.; Mo, Alisa; Hylton, Norma K.; DiTroia, Stephanie; Ganesh, Vijay S.; Smith, Richard S.; O’Kane, Katherine; Yeh, Rebecca C.; Marciano, Jack H.; Kirkham, Samantha; Kenny, Connor J.; Song, Janet H. T.; Al Saffar, Muna; Millan, Francisca; Harris, David J.; Murphy, Andrea V.; Klemp, Kara C.; Braddock, Stephen R.; Brand, Harrison; Wong, Isaac; Talkowski, Michael E.; [...]

    Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria

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    American Medical Association (AMA), 2023

    Published in: JAMA Neurology

  2. Mozaffarian, Dariush; Maki, Kevin C.; Bays, Harold E.; Aguilera, Fernando; Gould, Glenn; Hegele, Robert A.; Moriarty, Patrick M.; Robinson, Jennifer G.; Shi, Peilin; Tur, Josefina F.; Lapointe, Jean-François; Aziz, Sarya; Lemieux, Pierre; Hao, Tao; Mirza, Lubna; Kipp, Gaylon; Jarrett, Wentworth; Little, Raymond; Mariano, Hipolito; Nagajothi, Nagapradeep; Bender, Kevin; Everhart, Brian; Rahman, Syed; Usdan, Lisa; [...]

    Effectiveness of a Novel ω-3 Krill Oil Agent in Patients With Severe Hypertriglyceridemia : A Randomized Clinical Trial : A Randomized Clinical Trial

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    American Medical Association (AMA), 2022

    Published in: JAMA Network Open

  3. Kanca, Oguz; Andrews, Jonathan C.; Lee, Pei-Tseng; Patel, Chirag; Braddock, Stephen R.; Slavotinek, Anne M.; Cohen, Julie S.; Gubbels, Cynthia S.; Aldinger, Kimberly A.; Williams, Judy; Indaram, Maanasa; Fatemi, Ali; Yu, Timothy W.; Agrawal, Pankaj B.; Vezina, Gilbert; Simons, Cas; Crawford, Joanna; Lau, C. Christopher; Chung, Wendy K.; Markello, Thomas C.; Dobyns, William B.; Adams, David R.; Gahl, William A.; Wangler, Michael F.; [...]

    De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

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    Elsevier BV, 2019

    Published in: The American Journal of Human Genetics

  4. Kanca, Oguz; Andrews, Jonathan C.; Lee, Pei-Tseng; Patel, Chirag; Braddock, Stephen R.; Slavotinek, Anne M.; Cohen, Julie S.; Gubbels, Cynthia S.; Aldinger, Kimberly A.; Williams, Judy; Indaram, Maanasa; Fatemi, Ali; Yu, Timothy W.; Agrawal, Pankaj B.; Vezina, Gilbert; Simons, Cas; Crawford, Joanna; Lau, C. Christopher; Chung, Wendy K.; Markello, Thomas C.; Dobyns, William B.; Adams, David R.; Gahl, William A.; Wangler, Michael F.; [...]

    De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

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    Elsevier BV, 2019

    Published in: The American Journal of Human Genetics