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The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles. [electronic resource] by
- Kusenda, Mary
- Vacic, Vladimir
- Malhotra, Dheeraj
- Rodgers, Linda
- Pavon, Kevin
- Meth, Jennifer
- Kumar, Ravinesh A
- Christian, Susan L
- Peeters, Hilde
- Cho, Shawn S
- Addington, Anjene
- Rapoport, Judith L
- Sebat, Jonathan
Producer: 20160815
In:
Journal of child neurology vol. 30
Availability: No items available.
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8.
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A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. [electronic resource] by
- Kumar, Ravinesh A
- Sudi, Jyotsna
- Babatz, Timothy D
- Brune, Camille W
- Oswald, Donald
- Yen, Mayon
- Nowak, Norma J
- Cook, Edwin H
- Christian, Susan L
- Dobyns, William B
Producer: 20100506
In:
Journal of medical genetics vol. 47
Availability: No items available.
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9.
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Recurrent 16p11.2 microdeletions in autism. [electronic resource] by
- Kumar, Ravinesh A
- KaraMohamed, Samer
- Sudi, Jyotsna
- Conrad, Donald F
- Brune, Camille
- Badner, Judith A
- Gilliam, T Conrad
- Nowak, Norma J
- Cook, Edwin H
- Dobyns, William B
- Christian, Susan L
Producer: 20080312
In:
Human molecular genetics vol. 17
Availability: No items available.
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10.
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Selected summaries from the XVI World Congress of Psychiatric Genetics, Osaka, Japan, 11-15 October 2008. [electronic resource] by
- Bergen, Sarah
- Chen, Jingchun
- Dagdan, Elif
- Foon, Tee Shiau
- Goes, Fernando S
- Houlihan, Lorna M
- Kloiber, Stefan
- Kumar, Ravinesh A
- Kuzman, Martina Rojnic
- Menke, Andreas
- Pedroso, Inti
- Videtic, Alja
- Villafuerte, Sandra
- DeLisi, Lynn E
Producer: 20100209
In:
Psychiatric genetics vol. 19
Availability: No items available.
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11.
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TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins. [electronic resource] by
- Kumar, Ravinesh A
- Pilz, Daniela T
- Babatz, Timothy D
- Cushion, Thomas D
- Harvey, Kirsten
- Topf, Maya
- Yates, Laura
- Robb, Stephanie
- Uyanik, Gökhan
- Mancini, Gracia M S
- Rees, Mark I
- Harvey, Robert J
- Dobyns, William B
Producer: 20100928
In:
Human molecular genetics vol. 19
Availability: No items available.
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12.
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Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing. [electronic resource] by
- Kumar, Ravinesh A
- McGhee, Kevin A
- Leach, Stephen
- Bonaguro, Russell
- Maclean, Alan
- Aguirre-Hernandez, Rosalia
- Abrahams, Brett S
- Coccaro, Emil F
- Hodgins, Sheilagh
- Turecki, Gustavo
- Condon, Anne
- Muir, Walter J
- Brooks-Wilson, Angela R
- Blackwood, Douglas H
- Simpson, Elizabeth M
Producer: 20081204
In:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 147B
Availability: No items available.
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13.
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Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. [electronic resource] by
- Christian, Susan L
- Brune, Camille W
- Sudi, Jyotsna
- Kumar, Ravinesh A
- Liu, Shaung
- Karamohamed, Samer
- Badner, Judith A
- Matsui, Seiichi
- Conroy, Jeffrey
- McQuaid, Devin
- Gergel, James
- Hatchwell, Eli
- Gilliam, T Conrad
- Gershon, Elliot S
- Nowak, Norma J
- Dobyns, William B
- Cook, Edwin H
Producer: 20080815
In:
Biological psychiatry vol. 63
Availability: No items available.
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14.
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Association and mutation analyses of 16p11.2 autism candidate genes. [electronic resource] by
- Kumar, Ravinesh A
- Marshall, Christian R
- Badner, Judith A
- Babatz, Timothy D
- Mukamel, Zohar
- Aldinger, Kimberly A
- Sudi, Jyotsna
- Brune, Camille W
- Goh, Gerald
- Karamohamed, Samer
- Sutcliffe, James S
- Cook, Edwin H
- Geschwind, Daniel H
- Dobyns, William B
- Scherer, Stephen W
- Christian, Susan L
Producer: 20090428
In:
PloS one vol. 4
Availability: No items available.
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15.
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Microduplications of 16p11.2 are associated with schizophrenia. [electronic resource] by
- McCarthy, Shane E
- Makarov, Vladimir
- Kirov, George
- Addington, Anjene M
- McClellan, Jon
- Yoon, Seungtai
- Perkins, Diana O
- Dickel, Diane E
- Kusenda, Mary
- Krastoshevsky, Olga
- Krause, Verena
- Kumar, Ravinesh A
- Grozeva, Detelina
- Malhotra, Dheeraj
- Walsh, Tom
- Zackai, Elaine H
- Kaplan, Paige
- Ganesh, Jaya
- Krantz, Ian D
- Spinner, Nancy B
- Roccanova, Patricia
- Bhandari, Abhishek
- Pavon, Kevin
- Lakshmi, B
- Leotta, Anthony
- Kendall, Jude
- Lee, Yoon-Ha
- Vacic, Vladimir
- Gary, Sydney
- Iakoucheva, Lilia M
- Crow, Timothy J
- Christian, Susan L
- Lieberman, Jeffrey A
- Stroup, T Scott
- Lehtimäki, Terho
- Puura, Kaija
- Haldeman-Englert, Chad
- Pearl, Justin
- Goodell, Meredith
- Willour, Virginia L
- Derosse, Pamela
- Steele, Jo
- Kassem, Layla
- Wolff, Jessica
- Chitkara, Nisha
- McMahon, Francis J
- Malhotra, Anil K
- Potash, James B
- Schulze, Thomas G
- Nöthen, Markus M
- Cichon, Sven
- Rietschel, Marcella
- Leibenluft, Ellen
- Kustanovich, Vlad
- Lajonchere, Clara M
- Sutcliffe, James S
- Skuse, David
- Gill, Michael
- Gallagher, Louise
- Mendell, Nancy R
- Craddock, Nick
- Owen, Michael J
- O'Donovan, Michael C
- Shaikh, Tamim H
- Susser, Ezra
- Delisi, Lynn E
- Sullivan, Patrick F
- Deutsch, Curtis K
- Rapoport, Judith
- Levy, Deborah L
- King, Mary-Claire
- Sebat, Jonathan
Producer: 20091130
In:
Nature genetics vol. 41
Availability: No items available.
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