Joseph Buxbaum (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Joseph Buxbaum" in Spanish language version.

refsWebsite

Global rank Spanish rank

22nih.gov

4^th place

21issn.org

57^th place

3^rd place

21doi.org

2^nd place

6harvard.edu

18^th place

34^th place

2mssm.edu

low place

1mountsinai.org

low place

1archive.org

6^th place

5^th place

1inserm.fr

9,568^th place

low place

1scholar.google.com

1,697^th place

2,180^th place

1mhnews-autism.org

low place

1nam.edu

low place

archive.org (Global: 6^th place; Spanish: 5^th place)

Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret et al. (1 de febrero de 2012). «Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease». Neurobiology of Aging 33 (2): 416-417.e3. ISSN 1558-1497. PMC 4084881. PMID 20381196. doi:10.1016/j.neurobiolaging.2010.03.003.

doi.org (Global: 2^nd place; Spanish: 2^nd place)

dx.doi.org

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G. et al. (11 de octubre de 2005). «Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays». Proceedings of the National Academy of Sciences of the United States of America 102 (41): 14717-14722. Bibcode:2005PNAS..10214717F. ISSN 0027-8424. PMC 1253580. PMID 16203980. doi:10.1073/pnas.0506677102.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (1 de agosto de 2008). «A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders». Autism Research 1 (4): 251-257. ISSN 1939-3806. PMC 2678895. PMID 19360675. doi:10.1002/aur.30.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret et al. (1 de febrero de 2012). «Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease». Neurobiology of Aging 33 (2): 416-417.e3. ISSN 1558-1497. PMC 4084881. PMID 20381196. doi:10.1016/j.neurobiolaging.2010.03.003.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine et al. (10 de mayo de 2012). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature 485 (7397): 242-245. Bibcode:2012Natur.485..242N. ISSN 1476-4687. PMC 3613847. PMID 22495311. doi:10.1038/nature11011.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon et al. (3 de octubre de 2013). «Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder». American Journal of Human Genetics 93 (4): 607-619. ISSN 1537-6605. PMC 3791269. PMID 24094742. doi:10.1016/j.ajhg.2013.09.001.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina et al. (1 de agosto de 2014). «Most genetic risk for autism resides with common variation». Nature Genetics 46 (8): 881-885. ISSN 1546-1718. PMC 4137411. PMID 25038753. doi:10.1038/ng.3039.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li et al. (13 de noviembre de 2014). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature 515 (7526): 209-215. Bibcode:2014Natur.515..209.. ISSN 1476-4687. PMC 4402723. PMID 25363760. doi:10.1038/nature13772.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J. et al. (1 de agosto de 1990). «Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation». Proceedings of the National Academy of Sciences of the United States of America 87 (15): 6003-6006. Bibcode:1990PNAS...87.6003B. ISSN 0027-8424. PMC 54458. PMID 2116015. doi:10.1073/pnas.87.15.6003.
Buxbaum, J. D.; Liu, K. N.; Luo, Y.; Slack, J. L.; Stocking, K. L.; Peschon, J. J.; Johnson, R. S.; Castner, B. J. et al. (23 de octubre de 1998). «Evidence that tumor necrosis factor alpha converting enzyme is involved in regulated alpha-secretase cleavage of the Alzheimer amyloid protein precursor». The Journal of Biological Chemistry 273 (43): 27765-27767. ISSN 0021-9258. PMID 9774383. doi:10.1074/jbc.273.43.27765.
Näslund, J.; Haroutunian, V.; Mohs, R.; Davis, K. L.; Davies, P.; Greengard, P.; Buxbaum, J. D. (22 de marzo de 2000). «Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline». JAMA 283 (12): 1571-1577. ISSN 0098-7484. PMID 10735393. doi:10.1001/jama.283.12.1571.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing et al. (1 de septiembre de 2010). «Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities». PLOS Genetics 6 (9): e1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792. doi:10.1371/journal.pgen.1001130.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (10 de abril de 2001). «Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia». Proceedings of the National Academy of Sciences of the United States of America 98 (8): 4746-4751. Bibcode:2001PNAS...98.4746H. ISSN 0027-8424. PMC 31905. PMID 11296301. doi:10.1073/pnas.081071198.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N. et al. (1 de febrero de 2008). «Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene». Molecular Psychiatry 13 (2): 162-172. ISSN 1359-4184. PMC 5567789. PMID 17579610. doi:10.1038/sj.mp.4001991.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A. et al. (1 de enero de 2011). «Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes». Translational Psychiatry 1 (5): e8. ISSN 2158-3188. PMC 3309478. PMID 22832403. doi:10.1038/tp.2011.8.
Weiss, L. A.; Escayg, A.; Kearney, J. A.; Trudeau, M.; MacDonald, B. T.; Mori, M.; Reichert, J.; Buxbaum, J. D. et al. (1 de febrero de 2003). «Sodium channels SCN1A, SCN2A and SCN3A in familial autism». Molecular Psychiatry 8 (2): 186-194. ISSN 1359-4184. PMID 12610651. doi:10.1038/sj.mp.4001241.
Sanders, Stephan J.; He, Xin; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H. et al. (23 de septiembre de 2015). «Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci». Neuron 87 (6): 1215-1233. ISSN 1097-4199. PMC 4624267. PMID 26402605. doi:10.1016/j.neuron.2015.09.016.
Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W.; Autism Sequencing Consortium (20 de diciembre de 2012). «The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders». Neuron 76 (6): 1052-1056. ISSN 1097-4199. PMC 3863639. PMID 23259942. doi:10.1016/j.neuron.2012.12.008.
Bozdagi, Ozlem; Sakurai, Takeshi; Papapetrou, Danae; Wang, Xiaobin; Dickstein, Dara L.; Takahashi, Nagahide; Kajiwara, Yuji; Yang, Mu et al. (1 de enero de 2010). «Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication». Molecular Autism 1 (1): 15. ISSN 2040-2392. PMC 3019144. PMID 21167025. doi:10.1186/2040-2392-1-15.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita et al. (5 de julio de 2005). «Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene». Proceedings of the National Academy of Sciences of the United States of America 102 (27): 9643-9648. Bibcode:2005PNAS..102.9643S. ISSN 0027-8424. PMC 1160518. PMID 15983371. doi:10.1073/pnas.0503739102.
Kajiwara, Yuji; Schiff, Tamar; Voloudakis, Georgios; Gama Sosa, Miguel A.; Elder, Gregory; Bozdagi, Ozlem; Buxbaum, Joseph D. (1 de julio de 2014). «A critical role for human caspase-4 in endotoxin sensitivity». Journal of Immunology 193 (1): 335-343. ISSN 1550-6606. PMC 4066208. PMID 24879791. doi:10.4049/jimmunol.1303424.
Kolevzon, Alexander; Bush, Lauren; Wang, A. Ting; Halpern, Danielle; Frank, Yitzchak; Grodberg, David; Rapaport, Robert; Tavassoli, Teresa et al. (1 de enero de 2014). «A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome». Molecular Autism 5 (1): 54. ISSN 2040-2392. PMC 4326443. PMID 25685306. doi:10.1186/2040-2392-5-54.

harvard.edu (Global: 18^th place; Spanish: 34^th place)

adsabs.harvard.edu

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G. et al. (11 de octubre de 2005). «Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays». Proceedings of the National Academy of Sciences of the United States of America 102 (41): 14717-14722. Bibcode:2005PNAS..10214717F. ISSN 0027-8424. PMC 1253580. PMID 16203980. doi:10.1073/pnas.0506677102.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine et al. (10 de mayo de 2012). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature 485 (7397): 242-245. Bibcode:2012Natur.485..242N. ISSN 1476-4687. PMC 3613847. PMID 22495311. doi:10.1038/nature11011.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li et al. (13 de noviembre de 2014). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature 515 (7526): 209-215. Bibcode:2014Natur.515..209.. ISSN 1476-4687. PMC 4402723. PMID 25363760. doi:10.1038/nature13772.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J. et al. (1 de agosto de 1990). «Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation». Proceedings of the National Academy of Sciences of the United States of America 87 (15): 6003-6006. Bibcode:1990PNAS...87.6003B. ISSN 0027-8424. PMC 54458. PMID 2116015. doi:10.1073/pnas.87.15.6003.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (10 de abril de 2001). «Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia». Proceedings of the National Academy of Sciences of the United States of America 98 (8): 4746-4751. Bibcode:2001PNAS...98.4746H. ISSN 0027-8424. PMC 31905. PMID 11296301. doi:10.1073/pnas.081071198.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita et al. (5 de julio de 2005). «Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene». Proceedings of the National Academy of Sciences of the United States of America 102 (27): 9643-9648. Bibcode:2005PNAS..102.9643S. ISSN 0027-8424. PMC 1160518. PMID 15983371. doi:10.1073/pnas.0503739102.

inserm.fr (Global: 9,568^th place; Spanish: low place)

hal.inserm.fr

Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine et al. (10 de mayo de 2012). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature 485 (7397): 242-245. Bibcode:2012Natur.485..242N. ISSN 1476-4687. PMC 3613847. PMID 22495311. doi:10.1038/nature11011.

issn.org (Global: 57^th place; Spanish: 3^rd place)

portal.issn.org

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G. et al. (11 de octubre de 2005). «Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays». Proceedings of the National Academy of Sciences of the United States of America 102 (41): 14717-14722. Bibcode:2005PNAS..10214717F. ISSN 0027-8424. PMC 1253580. PMID 16203980. doi:10.1073/pnas.0506677102.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (1 de agosto de 2008). «A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders». Autism Research 1 (4): 251-257. ISSN 1939-3806. PMC 2678895. PMID 19360675. doi:10.1002/aur.30.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret et al. (1 de febrero de 2012). «Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease». Neurobiology of Aging 33 (2): 416-417.e3. ISSN 1558-1497. PMC 4084881. PMID 20381196. doi:10.1016/j.neurobiolaging.2010.03.003.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine et al. (10 de mayo de 2012). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature 485 (7397): 242-245. Bibcode:2012Natur.485..242N. ISSN 1476-4687. PMC 3613847. PMID 22495311. doi:10.1038/nature11011.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon et al. (3 de octubre de 2013). «Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder». American Journal of Human Genetics 93 (4): 607-619. ISSN 1537-6605. PMC 3791269. PMID 24094742. doi:10.1016/j.ajhg.2013.09.001.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina et al. (1 de agosto de 2014). «Most genetic risk for autism resides with common variation». Nature Genetics 46 (8): 881-885. ISSN 1546-1718. PMC 4137411. PMID 25038753. doi:10.1038/ng.3039.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li et al. (13 de noviembre de 2014). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature 515 (7526): 209-215. Bibcode:2014Natur.515..209.. ISSN 1476-4687. PMC 4402723. PMID 25363760. doi:10.1038/nature13772.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J. et al. (1 de agosto de 1990). «Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation». Proceedings of the National Academy of Sciences of the United States of America 87 (15): 6003-6006. Bibcode:1990PNAS...87.6003B. ISSN 0027-8424. PMC 54458. PMID 2116015. doi:10.1073/pnas.87.15.6003.
Buxbaum, J. D.; Liu, K. N.; Luo, Y.; Slack, J. L.; Stocking, K. L.; Peschon, J. J.; Johnson, R. S.; Castner, B. J. et al. (23 de octubre de 1998). «Evidence that tumor necrosis factor alpha converting enzyme is involved in regulated alpha-secretase cleavage of the Alzheimer amyloid protein precursor». The Journal of Biological Chemistry 273 (43): 27765-27767. ISSN 0021-9258. PMID 9774383. doi:10.1074/jbc.273.43.27765.
Näslund, J.; Haroutunian, V.; Mohs, R.; Davis, K. L.; Davies, P.; Greengard, P.; Buxbaum, J. D. (22 de marzo de 2000). «Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline». JAMA 283 (12): 1571-1577. ISSN 0098-7484. PMID 10735393. doi:10.1001/jama.283.12.1571.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing et al. (1 de septiembre de 2010). «Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities». PLOS Genetics 6 (9): e1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792. doi:10.1371/journal.pgen.1001130.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (10 de abril de 2001). «Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia». Proceedings of the National Academy of Sciences of the United States of America 98 (8): 4746-4751. Bibcode:2001PNAS...98.4746H. ISSN 0027-8424. PMC 31905. PMID 11296301. doi:10.1073/pnas.081071198.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N. et al. (1 de febrero de 2008). «Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene». Molecular Psychiatry 13 (2): 162-172. ISSN 1359-4184. PMC 5567789. PMID 17579610. doi:10.1038/sj.mp.4001991.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A. et al. (1 de enero de 2011). «Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes». Translational Psychiatry 1 (5): e8. ISSN 2158-3188. PMC 3309478. PMID 22832403. doi:10.1038/tp.2011.8.
Weiss, L. A.; Escayg, A.; Kearney, J. A.; Trudeau, M.; MacDonald, B. T.; Mori, M.; Reichert, J.; Buxbaum, J. D. et al. (1 de febrero de 2003). «Sodium channels SCN1A, SCN2A and SCN3A in familial autism». Molecular Psychiatry 8 (2): 186-194. ISSN 1359-4184. PMID 12610651. doi:10.1038/sj.mp.4001241.
Sanders, Stephan J.; He, Xin; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H. et al. (23 de septiembre de 2015). «Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci». Neuron 87 (6): 1215-1233. ISSN 1097-4199. PMC 4624267. PMID 26402605. doi:10.1016/j.neuron.2015.09.016.
Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W.; Autism Sequencing Consortium (20 de diciembre de 2012). «The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders». Neuron 76 (6): 1052-1056. ISSN 1097-4199. PMC 3863639. PMID 23259942. doi:10.1016/j.neuron.2012.12.008.
Bozdagi, Ozlem; Sakurai, Takeshi; Papapetrou, Danae; Wang, Xiaobin; Dickstein, Dara L.; Takahashi, Nagahide; Kajiwara, Yuji; Yang, Mu et al. (1 de enero de 2010). «Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication». Molecular Autism 1 (1): 15. ISSN 2040-2392. PMC 3019144. PMID 21167025. doi:10.1186/2040-2392-1-15.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita et al. (5 de julio de 2005). «Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene». Proceedings of the National Academy of Sciences of the United States of America 102 (27): 9643-9648. Bibcode:2005PNAS..102.9643S. ISSN 0027-8424. PMC 1160518. PMID 15983371. doi:10.1073/pnas.0503739102.
Kajiwara, Yuji; Schiff, Tamar; Voloudakis, Georgios; Gama Sosa, Miguel A.; Elder, Gregory; Bozdagi, Ozlem; Buxbaum, Joseph D. (1 de julio de 2014). «A critical role for human caspase-4 in endotoxin sensitivity». Journal of Immunology 193 (1): 335-343. ISSN 1550-6606. PMC 4066208. PMID 24879791. doi:10.4049/jimmunol.1303424.
Kolevzon, Alexander; Bush, Lauren; Wang, A. Ting; Halpern, Danielle; Frank, Yitzchak; Grodberg, David; Rapaport, Robert; Tavassoli, Teresa et al. (1 de enero de 2014). «A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome». Molecular Autism 5 (1): 54. ISSN 2040-2392. PMC 4326443. PMID 25685306. doi:10.1186/2040-2392-5-54.

mhnews-autism.org (Global: low place; Spanish: low place)

«ASN 2014 Awards Reception Journal». 4 de diciembre de 2014. Consultado el 9 de febrero de 2016.

mountsinai.org (Global: low place; Spanish: low place)

«Joseph D Buxbaum - The Mount Sinai Hospital». The Mount Sinai Hospital. Consultado el 27 de enero de 2016.

mssm.edu (Global: low place; Spanish: low place)

icahn.mssm.edu

«Directors | Icahn School of Medicine». Icahn School of Medicine at Mount Sinai. Consultado el 25 de enero de 2016.
«Joseph D Buxbaum - Icahn School of Medicine at Mount Sinai». Icahn School of Medicine at Mount Sinai.

nam.edu (Global: low place; Spanish: low place)

«NAM Elects 80 New Members». 19 de octubre de 2015.

nih.gov (Global: 4^th place; Spanish: 4^th place)

ncbi.nlm.nih.gov

Faham, Malek; Zheng, Jianbiao; Moorhead, Martin; Fakhrai-Rad, Hossein; Namsaraev, Eugeni; Wong, Kee; Wang, Zhiyong; Chow, Shu G. et al. (11 de octubre de 2005). «Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays». Proceedings of the National Academy of Sciences of the United States of America 102 (41): 14717-14722. Bibcode:2005PNAS..10214717F. ISSN 0027-8424. PMC 1253580. PMID 16203980. doi:10.1073/pnas.0506677102.
Sakurai, Takeshi; Reichert, Jennifer; Hoffman, Ellen J.; Cai, Guiqing; Jones, Hywel B.; Faham, Malek; Buxbaum, Joseph D. (1 de agosto de 2008). «A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders». Autism Research 1 (4): 251-257. ISSN 1939-3806. PMC 2678895. PMID 19360675. doi:10.1002/aur.30.
Cai, Guiqing; Atzmon, Gil; Naj, Adam C.; Beecham, Gary W.; Barzilai, Nir; Haines, Jonathan L.; Sano, Mary; Pericak-Vance, Margaret et al. (1 de febrero de 2012). «Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease». Neurobiology of Aging 33 (2): 416-417.e3. ISSN 1558-1497. PMC 4084881. PMID 20381196. doi:10.1016/j.neurobiolaging.2010.03.003.
Neale, Benjamin M.; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E.; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine et al. (10 de mayo de 2012). «Patterns and rates of exonic de novo mutations in autism spectrum disorders». Nature 485 (7397): 242-245. Bibcode:2012Natur.485..242N. ISSN 1476-4687. PMC 3613847. PMID 22495311. doi:10.1038/nature11011.
Poultney, Christopher S.; Goldberg, Arthur P.; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon et al. (3 de octubre de 2013). «Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder». American Journal of Human Genetics 93 (4): 607-619. ISSN 1537-6605. PMC 3791269. PMID 24094742. doi:10.1016/j.ajhg.2013.09.001.
Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J.; Bodea, Corneliu A.; Goldberg, Arthur P.; Lee, Ann B.; Mahajan, Milind; Manaa, Dina et al. (1 de agosto de 2014). «Most genetic risk for autism resides with common variation». Nature Genetics 46 (8): 881-885. ISSN 1546-1718. PMC 4137411. PMID 25038753. doi:10.1038/ng.3039.
De Rubeis, Silvia; He, Xin; Goldberg, Arthur P.; Poultney, Christopher S.; Samocha, Kaitlin; Cicek, A. Erucment; Kou, Yan; Liu, Li et al. (13 de noviembre de 2014). «Synaptic, transcriptional and chromatin genes disrupted in autism». Nature 515 (7526): 209-215. Bibcode:2014Natur.515..209.. ISSN 1476-4687. PMC 4402723. PMID 25363760. doi:10.1038/nature13772.
Buxbaum, J. D.; Gandy, S. E.; Cicchetti, P.; Ehrlich, M. E.; Czernik, A. J.; Fracasso, R. P.; Ramabhadran, T. V.; Unterbeck, A. J. et al. (1 de agosto de 1990). «Processing of Alzheimer beta/A4 amyloid precursor protein: modulation by agents that regulate protein phosphorylation». Proceedings of the National Academy of Sciences of the United States of America 87 (15): 6003-6006. Bibcode:1990PNAS...87.6003B. ISSN 0027-8424. PMC 54458. PMID 2116015. doi:10.1073/pnas.87.15.6003.
Buxbaum, J. D.; Liu, K. N.; Luo, Y.; Slack, J. L.; Stocking, K. L.; Peschon, J. J.; Johnson, R. S.; Castner, B. J. et al. (23 de octubre de 1998). «Evidence that tumor necrosis factor alpha converting enzyme is involved in regulated alpha-secretase cleavage of the Alzheimer amyloid protein precursor». The Journal of Biological Chemistry 273 (43): 27765-27767. ISSN 0021-9258. PMID 9774383. doi:10.1074/jbc.273.43.27765.
Näslund, J.; Haroutunian, V.; Mohs, R.; Davis, K. L.; Davies, P.; Greengard, P.; Buxbaum, J. D. (22 de marzo de 2000). «Correlation between elevated levels of amyloid beta-peptide in the brain and cognitive decline». JAMA 283 (12): 1571-1577. ISSN 0098-7484. PMID 10735393. doi:10.1001/jama.283.12.1571.
Naj, Adam C.; Beecham, Gary W.; Martin, Eden R.; Gallins, Paul J.; Powell, Eric H.; Konidari, Ioanna; Whitehead, Patrice L.; Cai, Guiqing et al. (1 de septiembre de 2010). «Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities». PLOS Genetics 6 (9): e1001130. ISSN 1553-7404. PMC 2944795. PMID 20885792. doi:10.1371/journal.pgen.1001130.
Hakak, Y.; Walker, J. R.; Li, C.; Wong, W. H.; Davis, K. L.; Buxbaum, J. D.; Haroutunian, V.; Fienberg, A. A. (10 de abril de 2001). «Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia». Proceedings of the National Academy of Sciences of the United States of America 98 (8): 4746-4751. Bibcode:2001PNAS...98.4746H. ISSN 0027-8424. PMC 31905. PMID 11296301. doi:10.1073/pnas.081071198.
Buxbaum, J. D.; Georgieva, L.; Young, J. J.; Plescia, C.; Kajiwara, Y.; Jiang, Y.; Moskvina, V.; Norton, N. et al. (1 de febrero de 2008). «Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene». Molecular Psychiatry 13 (2): 162-172. ISSN 1359-4184. PMC 5567789. PMID 17579610. doi:10.1038/sj.mp.4001991.
Takahashi, N.; Sakurai, T.; Bozdagi-Gunal, O.; Dorr, N. P.; Moy, J.; Krug, L.; Gama-Sosa, M.; Elder, G. A. et al. (1 de enero de 2011). «Increased expression of receptor phosphotyrosine phosphatase-β/ζ is associated with molecular, cellular, behavioral and cognitive schizophrenia phenotypes». Translational Psychiatry 1 (5): e8. ISSN 2158-3188. PMC 3309478. PMID 22832403. doi:10.1038/tp.2011.8.
Weiss, L. A.; Escayg, A.; Kearney, J. A.; Trudeau, M.; MacDonald, B. T.; Mori, M.; Reichert, J.; Buxbaum, J. D. et al. (1 de febrero de 2003). «Sodium channels SCN1A, SCN2A and SCN3A in familial autism». Molecular Psychiatry 8 (2): 186-194. ISSN 1359-4184. PMID 12610651. doi:10.1038/sj.mp.4001241.
Sanders, Stephan J.; He, Xin; Willsey, A. Jeremy; Ercan-Sencicek, A. Gulhan; Samocha, Kaitlin E.; Cicek, A. Ercument; Murtha, Michael T.; Bal, Vanessa H. et al. (23 de septiembre de 2015). «Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci». Neuron 87 (6): 1215-1233. ISSN 1097-4199. PMC 4624267. PMID 26402605. doi:10.1016/j.neuron.2015.09.016.
Buxbaum, Joseph D.; Daly, Mark J.; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W.; Autism Sequencing Consortium (20 de diciembre de 2012). «The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders». Neuron 76 (6): 1052-1056. ISSN 1097-4199. PMC 3863639. PMID 23259942. doi:10.1016/j.neuron.2012.12.008.
Bozdagi, Ozlem; Sakurai, Takeshi; Papapetrou, Danae; Wang, Xiaobin; Dickstein, Dara L.; Takahashi, Nagahide; Kajiwara, Yuji; Yang, Mu et al. (1 de enero de 2010). «Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication». Molecular Autism 1 (1): 15. ISSN 2040-2392. PMC 3019144. PMID 21167025. doi:10.1186/2040-2392-1-15.
Shu, Weiguo; Cho, Julie Y.; Jiang, Yuhui; Zhang, Minhua; Weisz, Donald; Elder, Gregory A.; Schmeidler, James; De Gasperi, Rita et al. (5 de julio de 2005). «Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene». Proceedings of the National Academy of Sciences of the United States of America 102 (27): 9643-9648. Bibcode:2005PNAS..102.9643S. ISSN 0027-8424. PMC 1160518. PMID 15983371. doi:10.1073/pnas.0503739102.
Kajiwara, Yuji; Schiff, Tamar; Voloudakis, Georgios; Gama Sosa, Miguel A.; Elder, Gregory; Bozdagi, Ozlem; Buxbaum, Joseph D. (1 de julio de 2014). «A critical role for human caspase-4 in endotoxin sensitivity». Journal of Immunology 193 (1): 335-343. ISSN 1550-6606. PMC 4066208. PMID 24879791. doi:10.4049/jimmunol.1303424.
Kolevzon, Alexander; Bush, Lauren; Wang, A. Ting; Halpern, Danielle; Frank, Yitzchak; Grodberg, David; Rapaport, Robert; Tavassoli, Teresa et al. (1 de enero de 2014). «A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome». Molecular Autism 5 (1): 54. ISSN 2040-2392. PMC 4326443. PMID 25685306. doi:10.1186/2040-2392-5-54.
«My Bibliography - My NCBI Collection». www.ncbi.nlm.nih.gov. Consultado el 10 de febrero de 2016.

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«Joseph D Buxbaum - Google Scholar Citations». scholar.google.com. Consultado el 12 de febrero de 2016.

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