Ethiopian Genetic Diversity Reveals Linguistic Stratification and Complex Influences on the Ethiopian Gene Pool von Pagani, Luca, Kivisild, Toomas, Tarekegn, Ayele, Ekong, Rosemary, Plaster, Chris, Gallego Romero, Irene, Ayub, Qasim, Mehdi, S. Qasim, Thomas, Mark G., Luiselli, Donata, Bekele, Endashaw, Bradman, Neil, Balding, David J., Tyler-Smith, Chris

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Where West Meets East: The Complex mtDNA Landscape of the Southwest and Central Asian Corridor von Quintana-Murci, Lluís, Chaix, Raphaëlle, Wells, R. Spencer, Behar, Doron M., Sayar, Hamid, Scozzari, Rosaria, Rengo, Chiara, Al-Zahery, Nadia, Semino, Ornella, Santachiara-Benerecetti, A. Silvana, Coppa, Alfredo, Ayub, Qasim, Mohyuddin, Aisha, Tyler-Smith, Chris, Qasim Mehdi, S., Torroni, Antonio, McElreavey, Ken

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Assessing the environmental justice implications of decarbonizing the US electric grid: estimating changes in asthma exacerbation by race and income von Mehdi, Qasim, Vasilakos, Petros

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The Kalash Genetic Isolate: Ancient divergence, drift and selection von Ayub, Qasim, Mezzavilla, Massimo, Pagani, Luca, Haber, Marc, Mohyuddin, Aisha, Khaliq, Shagufta, Mehdi, Syed Qasim, Tyler-Smith, Chris

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A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia von Dhandapany, Perundurai S, Sadayappan, Sakthivel, Xue, Yali, Powell, Gareth T, Rani, Deepa Selvi, Nallari, Prathiba, Rai, Taranjit Singh, Khullar, Madhu, Soares, Pedro, Bahl, Ajay, Tharkan, Jagan Mohan, Vaideeswar, Pradeep, Rathinavel, Andiappan, Narasimhan, Calambur, Ayapati, Dharma Rakshak, Ayub, Qasim, Mehdi, S Qasim, Oppenheimer, Stephen, Richards, Martin B, Price, Alkes L, Patterson, Nick, Reich, David, Singh, Lalji, Tyler-Smith, Chris, Thangaraj, Kumarasamy

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ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous von PRASOV, Lev, MASUD, Tehmina, KELBERMAN, Daniel, SOWDEN, Jane C, DATTANI, Mehul T, GLASER, Tom, KHALIQ, Shagufta, QASIM MEHDI, S, ABID, Aiysha, OLIVER, Edward R, SILVA, Eduardo D, LEWANDA, Amy, BRODSKY, Michael C, BORCHERT, Mark

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A Comprehensive Survey of Human Y-Chromosomal Microsatellites von Kayser, Manfred, Kittler, Ralf, Erler, Axel, Hedman, Minttu, Lee, Andrew C., Mohyuddin, Aisha, Mehdi, S. Qasim, Rosser, Zoë, Stoneking, Mark, Jobling, Mark A., Sajantila, Antti, Tyler-Smith, Chris

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Independent Introduction of Two Lactase-Persistence Alleles into Human Populations Reflects Different History of Adaptation to Milk Culture von Enattah, Nabil Sabri, Jensen, Tine G.K., Nielsen, Mette, Lewinski, Rikke, Kuokkanen, Mikko, Rasinpera, Heli, El-Shanti, Hatem, Seo, Jeong Kee, Alifrangis, Michael, Khalil, Insaf F., Natah, Abdrazak, Ali, Ahmed, Natah, Sirajedin, Comas, David, Mehdi, S. Qasim, Groop, Leif, Vestergaard, Else Marie, Imtiaz, Faiqa, Rashed, Mohamed S., Meyer, Brian, Troelsen, Jesper, Peltonen, Leena

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The Genetic Legacy of the Mongols von Zerjal, Tatiana, Xue, Yali, Bertorelle, Giorgio, Wells, R. Spencer, Bao, Weidong, Zhu, Suling, Qamar, Raheel, Ayub, Qasim, Mohyuddin, Aisha, Fu, Songbin, Li, Pu, Yuldasheva, Nadira, Ruzibakiev, Ruslan, Xu, Jiujin, Shu, Qunfang, Du, Ruofu, Yang, Huanming, Hurles, Matthew E., Robinson, Elizabeth, Gerelsaikhan, Tudevdagva, Dashnyam, Bumbein, Mehdi, S. Qasim, Tyler-Smith, Chris

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Geographically Separate Increases in the Frequency of the Derived ADH1B47His Allele in Eastern and Western Asia von Li, Hui, Mukherjee, Namita, Soundararajan, Usha, Tárnok, Zsanett, Barta, Csaba, Khaliq, Shagufta, Mohyuddin, Aisha, Kajuna, Sylvester L.B., Mehdi, S. Qasim, Kidd, Judith R., Kidd, Kenneth K.

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Y chromosome sequence variation and the history of human populations von Underhill, Peter A., Shen, Peidong, Lin, Alice A., Jin, Li, Passarino, Giuseppe, Yang, Wei H., Kauffman, Erin, Bonné-Tamir, Batsheva, Bertranpetit, Jaume, Francalacci, Paolo, Ibrahim, Muntaser, Jenkins, Trefor, Kidd, Judith R., Mehdi, S. Qasim, Seielstad, Mark T., Wells, R. Spencer, Piazza, Alberto, Davis, Ronald W., Feldman, Marcus W., Cavalli-Sforza, L. Luca, Oefner, Peter. J.

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Saving the Salmon: Examining the Cost-Effectiveness of Collaboration in Oregon von Mehdi, Qasim, Nabatchi, Tina

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Evidence of Still-Ongoing Convergence Evolution of the Lactase Persistence T -13910 Alleles in Humans von Enattah, Nabil Sabri, Trudeau, Aimee, Pimenoff, Ville, Maiuri, Luigi, Auricchio, Salvatore, Greco, Luigi, Rossi, Mauro, Lentze, Michael, Seo, J.K., Rahgozar, Soheila, Khalil, Insaf, Alifrangis, Michael, Natah, Sirajedin, Groop, Leif, Shaat, Nael, Kozlov, Andrew, Verschubskaya, Galina, Comas, David, Bulayeva, Kazima, Mehdi, S. Qasim, Terwilliger, Joseph D., Sahi, Timo, Savilahti, Erkki, Perola, Markus, Sajantila, Antti, Järvelä, Irma, Peltonen, Leena

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US Clean Energy Futures—Air Quality Benefits of Zero Carbon Energy Policies von Vasilakos, Petros N., Shen, Huizhong, Mehdi, Qasim, Wilcoxen, Peter, Driscoll, Charles, Fallon, Kathy, Burtraw, Dallas, Domeshek, Maya, Russell, Armistead G.

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Impact of Congenital Cardiac Catheterization Project on Outcomes-Quality Improvement (C3PO-QI) in LMICs von Ali, Fatima, Qasim Mehdi, Mohammad, Akhtar, Saleem, Aslam, Nadeem, Abbas, Rashid, Shah, Izat, Abidi, Jabbir, Arthur, Sajid, Nizar, Zeenat, Goodmann, Andrea, Bergersen, Lisa, Hasan, Babar

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"Like sugar in milk": reconstructing the genetic history of the Parsi population von Chaubey, Gyaneshwer, Ayub, Qasim, Rai, Niraj, Prakash, Satya, Mushrif-Tripathy, Veena, Mezzavilla, Massimo, Pathak, Ajai Kumar, Tamang, Rakesh, Firasat, Sadaf, Reidla, Maere, Karmin, Monika, Rani, Deepa Selvi, Reddy, Alla G, Parik, Jüri, Metspalu, Ene, Rootsi, Siiri, Dalal, Kurush, Khaliq, Shagufta, Mehdi, Syed Qasim, Singh, Lalji, Metspalu, Mait, Kivisild, Toomas, Tyler-Smith, Chris, Villems, Richard, Thangaraj, Kumarasamy

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Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis von Sohocki, Melanie M., Bowne, Sara J., Sullivan, Lori S., Blackshaw, Seth, Cepko, Constance L., Payne, Annette M., Bhattacharya, Shomi S., Khaliq, Shagufta, Qasim Mehdi, S., Birch, David G., Harrison, Wilbur R., Elder, Frederick F.B., Heckenlively, John R., Daiger, Stephen P.

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Sub-Saharan African coding sequence variation and haplotype diversity at the NAT2 gene von Patin, Etienne, Harmant, Christine, Kidd, Ken K., Kidd, Judith, Froment, Alain, Mehdi, S. Qasim, Sica, Lucas, Heyer, Evelyne, Quintana-Murci, Lluís

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Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography von Underhill, P A, Jin, L, Lin, A A, Mehdi, S Q, Jenkins, T, Vollrath, D, Davis, R W, Cavalli-Sforza, L L, Oefner, P J

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Refined Geographic Distribution of the Oriental ALDH2504Lys (nee 487Lys) Variant von Li, Hui, Borinskaya, Svetlana, Yoshimura, Kimio, Kal’ina, Nina, Marusin, Andrey, Stepanov, Vadim A., Qin, Zhendong, Khaliq, Shagufta, Lee, Mi‐Young, Yang, Yajun, Mohyuddin, Aisha, Gurwitz, David, Mehdi, Syed Qasim, Rogaev, Evgeny, Jin, Li, Yankovsky, Nikolay K., Kidd, Judith R., Kidd, Kenneth K.

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