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A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss. [electronic resource] by
- Hildebrand, Michael S
- Gandolfo, Luke
- Shearer, A Eliot
- Webster, Jennifer A
- Jensen, Maren
- Kimberling, William J
- Stephan, Dietrich
- Huygen, Patrick L M
- Smith, Richard J H
- Bahlo, Melanie
Producer: 20110120
In:
The Laryngoscope vol. 120
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Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss. [electronic resource] by
- Shearer, A Eliot
- Hildebrand, Michael S
- Webster, Jennifer A
- Kahrizi, Kimia
- Meyer, Nicole C
- Jalalvand, Khadijeh
- Arzhanginy, Sanaz
- Kimberling, William J
- Stephan, Dietrich
- Bahlo, Melanie
- Smith, Richard J H
- Najmabadi, Hossein
Producer: 20090427
In:
The Laryngoscope vol. 119
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Utilization of HER2 genetic testing in a multi-institutional observational study. [electronic resource] by
- Goddard, Katrina A B
- Bowles, Erin J Aiello
- Feigelson, Heather Spencer
- Habel, Laurel A
- Alford, Sharon Hensley
- McCarty, Catherine A
- Nekhlyudov, Larissa
- Onitilo, Adedayo A
- Rahm, Alanna K
- Webster, Jennifer A
Producer: 20131203
In:
The American journal of managed care vol. 18
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6.
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A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. [electronic resource] by
- Shearer, A Eliot
- Hildebrand, Michael S
- Bromhead, Catherine J
- Kahrizi, Kimia
- Webster, Jennifer A
- Azadeh, Batool
- Kimberling, William J
- Anousheh, Ali
- Nazeri, Arash
- Stephan, Dietrich
- Najmabadi, Hossein
- Smith, Richard J H
- Bahlo, Melanie
Producer: 20090416
In:
American journal of medical genetics. Part A vol. 149A
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Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies. [electronic resource] by
- Goddard, Katrina A B
- Whitlock, Evelyn P
- Berg, Jonathan S
- Williams, Marc S
- Webber, Elizabeth M
- Webster, Jennifer A
- Lin, Jennifer S
- Schrader, Kasmintan A
- Campos-Outcalt, Doug
- Offit, Kenneth
- Feigelson, Heather Spencer
- Hollombe, Celine
Producer: 20140310
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 15
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Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population. [electronic resource] by
- Hildebrand, Michael S
- Kahrizi, Kimia
- Bromhead, Catherine J
- Shearer, A Eliot
- Webster, Jennifer A
- Khodaei, Hossein
- Abtahi, Rezvan
- Bazazzadegan, Niloofar
- Babanejad, Mojgan
- Nikzat, Nooshin
- Kimberling, William J
- Stephan, Dietrich
- Huygen, Patrick L M
- Bahlo, Melanie
- Smith, Richard J H
- Najmabadi, Hossein
Producer: 20110223
In:
The Annals of otology, rhinology, and laryngology vol. 119
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9.
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Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. [electronic resource] by
- Grillet, Nicolas
- Schwander, Martin
- Hildebrand, Michael S
- Sczaniecka, Anna
- Kolatkar, Anand
- Velasco, Janice
- Webster, Jennifer A
- Kahrizi, Kimia
- Najmabadi, Hossein
- Kimberling, William J
- Stephan, Dietrich
- Bahlo, Melanie
- Wiltshire, Tim
- Tarantino, Lisa M
- Kuhn, Peter
- Smith, Richard J H
- Müller, Ulrich
Producer: 20090930
In:
American journal of human genetics vol. 85
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10.
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A survey of genetic human cortical gene expression. [electronic resource] by
- Myers, Amanda J
- Gibbs, J Raphael
- Webster, Jennifer A
- Rohrer, Kristen
- Zhao, Alice
- Marlowe, Lauren
- Kaleem, Mona
- Leung, Doris
- Bryden, Leslie
- Nath, Priti
- Zismann, Victoria L
- Joshipura, Keta
- Huentelman, Matthew J
- Hu-Lince, Diane
- Coon, Keith D
- Craig, David W
- Pearson, John V
- Holmans, Peter
- Heward, Christopher B
- Reiman, Eric M
- Stephan, Dietrich
- Hardy, John
Producer: 20071211
In:
Nature genetics vol. 39
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11.
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A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. [electronic resource] by
- Coon, Keith D
- Myers, Amanda J
- Craig, David W
- Webster, Jennifer A
- Pearson, John V
- Lince, Diane Hu
- Zismann, Victoria L
- Beach, Thomas G
- Leung, Doris
- Bryden, Leslie
- Halperin, Rebecca F
- Marlowe, Lauren
- Kaleem, Mona
- Walker, Douglas G
- Ravid, Rivka
- Heward, Christopher B
- Rogers, Joseph
- Papassotiropoulos, Andreas
- Reiman, Eric M
- Hardy, John
- Stephan, Dietrich A
Producer: 20070510
In:
The Journal of clinical psychiatry vol. 68
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12.
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Sorl1 as an Alzheimer's disease predisposition gene? [electronic resource] by
- Webster, Jennifer A
- Myers, Amanda J
- Pearson, John V
- Craig, David W
- Hu-Lince, Diane
- Coon, Keith D
- Zismann, Victoria L
- Beach, Thomas
- Leung, Doris
- Bryden, Leslie
- Halperin, Rebecca F
- Marlowe, Lauren
- Kaleem, Mona
- Huentelman, Matthew J
- Joshipura, Keta
- Walker, Douglas
- Heward, Christopher B
- Ravid, Rivka
- Rogers, Joseph
- Papassotiropoulos, Andreas
- Hardy, John
- Reiman, Eric M
- Stephan, Dietrich A
Producer: 20080425
In:
Neuro-degenerative diseases vol. 5
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13.
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Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies. [electronic resource] by
- Pearson, John V
- Huentelman, Matthew J
- Halperin, Rebecca F
- Tembe, Waibhav D
- Melquist, Stacey
- Homer, Nils
- Brun, Marcel
- Szelinger, Szabolcs
- Coon, Keith D
- Zismann, Victoria L
- Webster, Jennifer A
- Beach, Thomas
- Sando, Sigrid B
- Aasly, Jan O
- Heun, Reinhard
- Jessen, Frank
- Kolsch, Heike
- Tsolaki, Magdalini
- Daniilidou, Makrina
- Reiman, Eric M
- Papassotiropoulos, Andreas
- Hutton, Michael L
- Stephan, Dietrich A
- Craig, David W
Producer: 20070212
In:
American journal of human genetics vol. 80
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14.
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Genetic control of human brain transcript expression in Alzheimer disease. [electronic resource] by
- Webster, Jennifer A
- Gibbs, J Raphael
- Clarke, Jennifer
- Ray, Monika
- Zhang, Weixiong
- Holmans, Peter
- Rohrer, Kristen
- Zhao, Alice
- Marlowe, Lauren
- Kaleem, Mona
- McCorquodale, Donald S
- Cuello, Cindy
- Leung, Doris
- Bryden, Leslie
- Nath, Priti
- Zismann, Victoria L
- Joshipura, Keta
- Huentelman, Matthew J
- Hu-Lince, Diane
- Coon, Keith D
- Craig, David W
- Pearson, John V
- Heward, Christopher B
- Reiman, Eric M
- Stephan, Dietrich
- Hardy, John
- Myers, Amanda J
Producer: 20090424
In:
American journal of human genetics vol. 84
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15.
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Evidence for an association between KIBRA and late-onset Alzheimer's disease. [electronic resource] by
- Corneveaux, Jason J
- Liang, Winnie S
- Reiman, Eric M
- Webster, Jennifer A
- Myers, Amanda J
- Zismann, Victoria L
- Joshipura, Keta D
- Pearson, John V
- Hu-Lince, Diane
- Craig, David W
- Coon, Keith D
- Dunckley, Travis
- Bandy, Daniel
- Lee, Wendy
- Chen, Kewei
- Beach, Thomas G
- Mastroeni, Diego
- Grover, Andrew
- Ravid, Rivka
- Sando, Sigrid B
- Aasly, Jan O
- Heun, Reinhard
- Jessen, Frank
- Kölsch, Heike
- Rogers, Joseph
- Hutton, Michael L
- Melquist, Stacey
- Petersen, Ron C
- Alexander, Gene E
- Caselli, Richard J
- Papassotiropoulos, Andreas
- Stephan, Dietrich A
- Huentelman, Matthew J
Producer: 20100713
In:
Neurobiology of aging vol. 31
Availability: No items available.
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16.
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GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. [electronic resource] by
- Reiman, Eric M
- Webster, Jennifer A
- Myers, Amanda J
- Hardy, John
- Dunckley, Travis
- Zismann, Victoria L
- Joshipura, Keta D
- Pearson, John V
- Hu-Lince, Diane
- Huentelman, Matthew J
- Craig, David W
- Coon, Keith D
- Liang, Winnie S
- Herbert, RiLee H
- Beach, Thomas
- Rohrer, Kristen C
- Zhao, Alice S
- Leung, Doris
- Bryden, Leslie
- Marlowe, Lauren
- Kaleem, Mona
- Mastroeni, Diego
- Grover, Andrew
- Heward, Christopher B
- Ravid, Rivka
- Rogers, Joseph
- Hutton, Michael L
- Melquist, Stacey
- Petersen, Ron C
- Alexander, Gene E
- Caselli, Richard J
- Kukull, Walter
- Papassotiropoulos, Andreas
- Stephan, Dietrich A
Producer: 20070731
In:
Neuron vol. 54
Availability: No items available.
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17.
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Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. [electronic resource] by
- Borck, Guntram
- Ur Rehman, Atteeq
- Lee, Kwanghyuk
- Pogoda, Hans-Martin
- Kakar, Naseebullah
- von Ameln, Simon
- Grillet, Nicolas
- Hildebrand, Michael S
- Ahmed, Zubair M
- Nürnberg, Gudrun
- Ansar, Muhammad
- Basit, Sulman
- Javed, Qamar
- Morell, Robert J
- Nasreen, Nabilah
- Shearer, A Eliot
- Ahmad, Adeel
- Kahrizi, Kimia
- Shaikh, Rehan S
- Ali, Rana A
- Khan, Shaheen N
- Goebel, Ingrid
- Meyer, Nicole C
- Kimberling, William J
- Webster, Jennifer A
- Stephan, Dietrich A
- Schiller, Martin R
- Bahlo, Melanie
- Najmabadi, Hossein
- Gillespie, Peter G
- Nürnberg, Peter
- Wollnik, Bernd
- Riazuddin, Saima
- Smith, Richard J H
- Ahmad, Wasim
- Müller, Ulrich
- Hammerschmidt, Matthias
- Friedman, Thomas B
- Riazuddin, Sheikh
- Leal, Suzanne M
- Ahmad, Jamil
- Kubisch, Christian
Producer: 20110329
In:
American journal of human genetics vol. 88
Availability: No items available.
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