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American Journal of Human Geneticsжурнал

Статьи, опубликованные в журнале

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  • 2018 Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
  • Ganna Andrea, Kyle Satterstrom F., Zekavat Seyedeh M., Das Indraniel, Kurki Mitja I., Churchhouse Claire, Alfoldi Jessica, Martin Alicia R., Havulinna Aki S., Byrnes Andrea, Thompson Wesley K., Nielsen Philip R., Karczewski Konrad J., Saarentaus Elmo, Rivas Manuel A., Gupta Namrata, Pietiläinen Olli, Emdin Connor A., Lescai Francesco, Bybjerg-Grauholm Jonas, Flannick Jason, Mercader Josep M., Udler Miriam, Laakso Markku, Salomaa Veikko, Hultman Christina, Ripatti Samuli, Hämäläinen Eija, Moilanen Jukka S., Körkkö Jarmo, Kuismin Outi, Nordentoft Merete, Hougaard David M., Mors Ole, Werge Thomas, Mortensen Preben Bo, MacArthur Daniel, Daly Mark J., Sullivan Patrick F., Locke Adam E., Palotie Aarno, Børglum Anders D., Kathiresan Sekar, Neale Benjamin M.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 102, № 6, с. 1204-1211
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  • 2018 Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
  • Ganna Andrea, Kyle Satterstrom F., Zekavat Seyedeh M., Das Indraniel, Kurki Mitja I., Churchhouse Claire, Alfoldi Jessica, Martin Alicia R., Havulinna Aki S., Byrnes Andrea, Thompson Wesley K., Nielsen Philip R., Karczewski Konrad J., Saarentaus Elmo, Rivas Manuel A., Gupta Namrata, Pietiläinen Olli, Emdin Connor A., Lescai Francesco, Bybjerg-Grauholm Jonas, Flannick Jason, Mercader Josep M., Udler Miriam, Laakso Markku, Salomaa Veikko, Hultman Christina, Ripatti Samuli, Hämäläinen Eija, Moilanen Jukka S., Körkkö Jarmo, Kuismin Outi, Nordentoft Merete, Hougaard David M., Mors Ole, Werge Thomas, Mortensen Preben Bo, MacArthur Daniel, Daly Mark J., Sullivan Patrick F., Locke Adam E., Palotie Aarno, Børglum Anders D., Kathiresan Sekar, Neale Benjamin M.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 102, № 6, с. 1204-1211
• 
  • 2018 Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
  • Ganna Andrea, Kyle Satterstrom F., Zekavat Seyedeh M., Das Indraniel, Kurki Mitja I., Churchhouse Claire, Alfoldi Jessica, Martin Alicia R., Havulinna Aki S., Byrnes Andrea, Thompson Wesley K., Nielsen Philip R., Karczewski Konrad J., Saarentaus Elmo, Rivas Manuel A., Gupta Namrata, Pietiläinen Olli, Emdin Connor A., Lescai Francesco, Bybjerg-Grauholm Jonas, Flannick Jason, Mercader Josep M., Udler Miriam, Laakso Markku, Salomaa Veikko, Hultman Christina, Ripatti Samuli, Hämäläinen Eija, Moilanen Jukka S., Körkkö Jarmo, Kuismin Outi, Nordentoft Merete, Hougaard David M., Mors Ole, Werge Thomas, Mortensen Preben Bo, MacArthur Daniel, Daly Mark J., Sullivan Patrick F., Locke Adam E., Palotie Aarno, Børglum Anders D., Kathiresan Sekar, Neale Benjamin M.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 102, № 6, с. 1204-1211
• 
  • 2018 Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
  • Ganna Andrea, Kyle Satterstrom F., Zekavat Seyedeh M., Das Indraniel, Kurki Mitja I., Churchhouse Claire, Alfoldi Jessica, Martin Alicia R., Havulinna Aki S., Byrnes Andrea, Thompson Wesley K., Nielsen Philip R., Karczewski Konrad J., Saarentaus Elmo, Rivas Manuel A., Gupta Namrata, Pietiläinen Olli, Emdin Connor A., Lescai Francesco, Bybjerg-Grauholm Jonas, Flannick Jason, Mercader Josep M., Udler Miriam, Laakso Markku, Salomaa Veikko, Hultman Christina, Ripatti Samuli, Hämäläinen Eija, Moilanen Jukka S., Körkkö Jarmo, Kuismin Outi, Nordentoft Merete, Hougaard David M., Mors Ole, Werge Thomas, Mortensen Preben Bo, MacArthur Daniel, Daly Mark J., Sullivan Patrick F., Locke Adam E., Palotie Aarno, Børglum Anders D., Kathiresan Sekar, Neale Benjamin M.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 102, № 6, с. 1204-1211
• 
  • 2018 Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
  • Ganna Andrea, Kyle Satterstrom F., Zekavat Seyedeh M., Das Indraniel, Kurki Mitja I., Churchhouse Claire, Alfoldi Jessica, Martin Alicia R., Havulinna Aki S., Byrnes Andrea, Thompson Wesley K., Nielsen Philip R., Karczewski Konrad J., Saarentaus Elmo, Rivas Manuel A., Gupta Namrata, Pietiläinen Olli, Emdin Connor A., Lescai Francesco, Bybjerg-Grauholm Jonas, Flannick Jason, Mercader Josep M., Udler Miriam, Laakso Markku, Salomaa Veikko, Hultman Christina, Ripatti Samuli, Hämäläinen Eija, Moilanen Jukka S., Körkkö Jarmo, Kuismin Outi, Nordentoft Merete, Hougaard David M., Mors Ole, Werge Thomas, Mortensen Preben Bo, MacArthur Daniel, Daly Mark J., Sullivan Patrick F., Locke Adam E., Palotie Aarno, Børglum Anders D., Kathiresan Sekar, Neale Benjamin M.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 102, № 6, с. 1204-1211
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  • 2018 Understanding the Hidden Complexity of Latin American Population Isolates
  • Mooney Jazlyn A., Huber Christian D., Service Susan, Sul Jae Hoon, Marsden Clare D., Zhang Zhongyang, Sabatti Chiara, Ruiz-Linares Andrés, Bedoya Gabriel, Freimer Nelson, Lohmueller Kirk E., Fears Scott C., Kremeyer Barbara, Lic Carmen Araya, Lic Xinia Araya, Bejarano Julio, Lic Margarita Ramirez, Castrillón Gabriel, Lopez Maria C., Montoya Gabriel, Montoya Patricia, Teshiba Terri M., Altshuler Lori, Bartzokis George, Escobar Javier, Ospina-Duque Jorge, Risch Neil, Ruiz-Linares Andrés, Cantor Rita M., Lopez-Jaramillo Carlos, Macaya Gabriel, Molina Julio, Reus Victor I., Bearden Carrie E., Sul Jae Hoon, Huang Alden Y., Ramensky Vasily, Hwang Sun-Goo, Park YoungJun, Zhang Zhongyang, Loohuis Loes M.Olde, Spesny Mitzi, Gomez-Makhinson Juliana, Bedoya Gabriel, Coppola Giovanni
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 103, № 5, с. 707-726
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  • 2016 Human Y Chromosome Haplogroup N: A Non-trivial Time-Resolved Phylogeography that Cuts across Language Families
  • Anne-Mai Ilumäe, Maere Reidla, Marina Chukhryaeva, Mari Järve, Helen Post, Monika Karmin, Lauri Saag, Anastasiya Agdzhoyan, Alena Kushniarevich, Sergey Litvinov, Natalya Ekomasova, Kristiina Tambets, Ene Metspalu, Rita Khusainova, Bayazit Yunusbayev, Khusnutdinova Elza K., Osipova Ludmila P., Sardana Fedorova, Olga Utevska, Sergey Koshel, Elena Balanovska, Behar Doron M., Oleg Balanovsky, Toomas Kivisild, Underhill Peter A., Richard Villems, Siiri Rootsi
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 99, № 1, с. 163-173 DOI
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  • 2014 Gene age predicts the strength of purifying selection acting on gene expression variation in humans
  • Popadin Konstantin Y., Gutierrez-Arcelus Maria, Lappalainen Tuuli, Buil Alfonso, Steinberg Julia, Nikolaev Sergey I., Lukowski Samuel W., Bazykin Georgii A., Seplyarskiy Vladimir B., Ioannidis Panagiotis, Zdobnov Evgeny M., Dermitzakis Emmanouil T., Antonarakis Stylianos E.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 95, № 6, с. 660-674 DOI
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  • 2011 Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74
  • Ahmed Zubair M., Yousaf Rizwan, Lee Byung Cheon, Khan Shaheen N., Lee Sue, Lee Kwanghyuk, Husnain Tayyab, Rehman Atteeq Ur, Bonneux Sarah, Ansar Muhammad, Ahmad Wasim, Leal Suzanne M., Gladyshev Vadim N., Belyantseva Inna A., Camp Guy Van, Riazuddin Sheikh, Friedman Thomas B., Riazuddin Saima
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 88, № 1, с. 19-29
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  • 2009 Distribution of the alcohol dehydrogenase ADH1B*47His allele in Eurasia
  • Borinskaya S., Kal'ina N., Marusin A., Faskhutdinova G., Morozova I., Kutuev I., Koshechkin V., Khusnutdinova E., Stepanov V., Puzyrev V., Yankovsky N., Rogaev E.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 84, № 1, с. 89-92
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  • 2008 Positive selection in alternatively spliced exons of human genes
  • Ramensky Vasily E., Nurtdinov Ramil N., Neverov Alexei D., Mironov Andrei A., Gelfand Mikhail S.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 83, № 1, с. 94-98
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  • 2007 Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state
  • Plotnikova OV, Kondrashov FA, Vlasov PK, Grigorenko AP, Ginter EK, Rogaev EI
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 81, № 1, с. 32-43
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  • 2007 Evidence for still ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
  • Enattah N.S., Trudeau A., Pimenoff V., Maiuri L., Auricchio S., Creco L., Rossi M., Lentze M., Seo J.K., Rahgozar S., Khalil I., Alifrangis M., Natah S., Groop L., Shaat N., Kozlov A., Verschubskaya G., Comas D., Bulaeva K., Mehdi S.Q., Terwilliger J.D., Sahi T., Savilahti E., Perola M., Sajantila A., Järvelä I., Peltonen L.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 81, с. 615-625
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  • 2005 Quantitative founder effect analysis of French-Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension. Am.J.Hum.Genet
  • Hamet P., Merlo E., Seda O., Broeckel U., Tremblay J., Kaldunski M., Gaudet D., Bouchard G., Deslauriers B., Gagnon F., Antoniol G., Pausova Z., Labuda M., Jompe M., Gossard F., Kirova R., Tonellato P., Orlov S.N., Pintos J., Platko J., Hudson T.J., Rioux J.D., Kotchen T.A., Cowley AW
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 76, с. 815-832
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  • 2003 Multiple Origins of Ashkenazi Levites: Y Chromosome Evidence for Both Near Eastern and European Ancestries
  • Behar D.M., Thomas M.G., Skorecki K., Hammer M.F., Bulygina E., Rosengarten D., Jones A.L., Held K., Moses V., Goldstein D., Bradman N., Weale M.E.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 73, с. 768-779 DOI
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  • 2002 Population data on DIS80 in different ethnic groups of Russia and Belarus
  • Verbenko D.A., Kekeeva T.V., Khusnutdinova E.K., Pogoda T.V., Spitsyn V.A., Mikulich A.I., Bebyakova N.A., Bets L.V., Ivanov V.P., Abolmasov N.N., Tarskaya L.A., Sorensen M.V., Limborskaya S.A.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 71, № 4, с. 354-354
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  • 2001 Lactase haplotype diversity in the Old World
  • Hollox E., Poulter M., Zvarik M., Ferak V., Krause A., Jenkins T., Saha N., Kozlov A., Swallow D.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 68, с. 160-172
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  • 2000 Perturbation of the developing chick embryo using antisense to fibrillin-1
  • Plaza S., Zhou G., Belleh S., Vinogradov S.V., Kabanov A.V., Godfrey M.
  • в журнале American Journal of Human Genetics, издательство University of Chicago Press (United States), том 67, № 4, с. 172-172