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D

Dan Geiger

Hebrew University of Jerusalem

53H指数
167论文数
1.8W被引数
收录论文 30
发表时间
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Polyadenylation and degradation of human mitochondrial RNA: the prokaryotic past leaves its mark
errMOLECULAR AND CELLULAR BIOLOGY
IF2.7
err2023-03-27
err163
errOAAI
errSlomovic, S; Laufer, D; Geiger, D; Schuster, G
err分享
err收藏
Estimating variance components in population scale family trees估计人口规模家谱中的方差分量
errPLOS GENETICS
IF3.7
err2019-05-09
err10
errOAAI
errShor, Tal; Kalka, Iris; Geiger, Dan; Erlich, Yaniv; Weissbrod, Omer
err分享
err收藏
Genetic linkage analysis of a large family identifies FIGN as a candidate modulator of reduced penetrance in heritable pulmonary arterial hypertension
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2019-03-20
err3
errOAAI
errPuigdevall, Pau; Piccari, Lucilla; Blanco, Isabel; Barbera, Joan Albert; Geiger, Dan; Badenas, Celia; Mila, Montserrat; Castelo, Robert; Madrigal, Irene
err分享
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Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2018-03-15
err18
errOAAI
errShalata, Adel; Mahroom, Mohammad; Milewicz, Dianna M.; Gong Limin; Kassum, Fadi; Badarna, Khader; Tarabeih, Nader; Assy, Nimmer; Fell, Rona; Cohen, Hector; Nashashibi, Munir; Livoff, Alejandro; Azab, Muhammad; Habib, George; Geiger, Dan; Weissbrod, Omer; Nseir, William
err分享
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Loss of CD55 in Eculizumab-Responsive Protein-Losing Enteropathy
errNEW ENGLAND JOURNAL OF MEDICINE
IF78.5
err2017-07-06
err54
errOAAI
errKurolap, Alina; Eshach-Adiv, Orly; Hershkovitz, Tova; Paperna, Tamar; Mory, Adi; Oz-Levi, Danit; Zohar, Yaniv; Mandel, Hanna; Chezar, Judith; Azoulay, David; Peleg, Sarit; Half, Elizabeth E.; Yahalom, Vered; Finkel, Lilach; Weissbrod, Omer; Geiger, Dan; Tabib, Adi; Shaoul, Ron; Magen, Daniella; Bonstein, Lilach; Mevorach, Dror; Baris, Hagit N.
err分享
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IMMUNOGENICITY OF ANTI-TNF DRUGS AND CLINICAL RESPONSE IN PATIENTS WITH SPONDYLOARTHRITIS
errANNALS OF THE RHEUMATIC DISEASES
IF20.6
err2017-06-01
err0
errOAAI
errGeiger, D.; Degboe, Y.; Barnetche, T.; Cantagrel, A.; Ruyssen-Witrand, A.; Constantin, A.
err分享
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Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy
errBRAIN
IF11.7
err2016-12-21
err18
errOAAI
errFalik Zaccai, Tzipora C.; Savitzki, David; Zivony-Elboum, Yifat; Vilboux, Thierry; Fitts, Eric C.; Shoval, Yishay; Kalfon, Limor; Samra, Nadra; Keren, Zohar; Gross, Bella; Chasnyk, Natalia; Straussberg, Rachel; Mullikin, James C.; Teer, Jamie K.; Geiger, Dan; Kornitzer, Daniel; Bitterman-Deutsch, Ora; Samson, Abraham O.; Wakamiya, Maki; Peterson, Johnny W.; Kirtley, Michelle L.; Pinchuk, Iryna, V; Baze, Wallace B.; Gahl, William A.; Kleta, Robert; Anikster, Yair; Chopra, Ashok K.
err分享
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Multikernel linear mixed models for complex phenotype prediction
errGENOME RESEARCH
IF5.5
err2016-06-14
err44
errOAAI
errWeissbrod, Omer; Geiger, Dan; Rosset, Saharon
err分享
err收藏
Accurate liability estimation improves power in ascertained case-control studies
errNATURE METHODS
IF32.1
err2015-02-09
err28
errOAAI
errWeissbrod, Omer; Lippert, Christoph; Geiger, Dan; Heckerman, David
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Induced pluripotent stem cells as a model for telomeric abnormalities in ICF type I syndrome
errHUMAN MOLECULAR GENETICS
IF3.2
err2014-02-18
err30
errOAAI
errSagie, Shira; Ellran, Erika; Katzir, Hagar; Shaked, Rony; Yehezkel, Shiran; Laevsky, Ilana; Ghanayim, Alaa; Geiger, Dan; Tzukerman, Maty; Selig, Sara
err分享
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Titin Mutation in Familial Restrictive Cardiomyopathy
errINTERNATIONAL JOURNAL OF CARDIOLOGY
IF3.2
err2014-01-01
err83
PREAI
errPeled, Yael; Gramlich, Michael; Yoskovitz, Guy; Feinberg, Micha S.; Afek, Arnon; Polak-Charcon, Sylvie; Pras, Elon; Sela, Ben-Ami; Konen, Eli; Weissbrod, Omer; Geiger, Dan; Gordon, Paul M. K.; Thierfelder, Ludwig; Freimark, Dov; Gerull, Brenda; Arad, Michael
err分享
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Population-Specific Association between a Polymorphic Variant in ST18, Encoding a Pro-Apoptotic Molecule, and Pemphigus Vulgans
errJOURNAL OF INVESTIGATIVE DERMATOLOGY
IF5.7
err2012-07-01
err77
errOAAI
errSarig, Ofer; Bercovici, Sivan; Zoller, Lilach; Goldberg, Ilan; Indelman, Margarita; Nahum, Sagi; Israeli, Shirli; Sagiv, Nadav; de Morentin, Helena Martinez; Katz, Oren; Baun, Sharon; Barzilai, Aviv; Trau, Henri; Murrell, Dedee F.; Bergman, Reuven; Hertl, Michael; Rosenberg, Shai; Noethen, Markus M.; Skorecki, Karl; Schmidt, Enno; Zillikens, Detlef; Darvasi, Ariel; Geiger, Dan; Rosset, Saharon; Ibrahim, Saleh M.; Sprecher, Eli
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A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2012-06-20
err65
PREAI
errZivony-Elboum, Yifat; Westbroek, Wendy; Kfir, Nehama; Savitzki, David; Shoval, Yishay; Bloom, Assnat; Rod, Raya; Khayat, Morad; Gross, Bella; Samri, Walid; Cohen, Hector; Sonkin, Vadim; Freidman, Tatiana; Geiger, Dan; Fattal-Valevski, Aviva; Anikster, Yair; Waters, Aoife M.; Kleta, Robert; Falik-Zaccai, Tzipora C.
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Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3-13.1
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2010-02-10
err5
errOAAI
errGenzer-Nir, Mira; Khayat, Morad; Kogan, Leonid; Cohen, Hector I.; Hershkowitz, Miriam; Geiger, Dan; Falik-Zaccai, Tzipora C.
err分享
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Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2009-08-01
err139
errOAAI
errRenbaum, Paul; Kellerman, Efrat; Jaron, Ranit; Geiger, Dan; Segel, Reeval; Lee, Ming; King, Mary Claire; Levy-Lahad, Ephrat
err分享
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Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesis
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2008-05-01
err71
errOAAI
errNousbeck, Janna; Spiegel, Ronen; Ishida-Yamamoto, Akemi; Indelman, Margarita; Shani-Adir, Ayelet; Adir, Noam; Lipkin, Ehud; Bercovici, Sivan; Geiger, Dan; van Steensel, Maurice A.; Steijlen, Peter M.; Bergman, Reuven; Bindereif, Albrecht; Choder, Mordechai; Shalev, Stavit; Sprecher, Eli
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Panel construction for mapping in admixed populations via expected mutual information
errGENOME RESEARCH
IF5.5
err2008-03-18
err12
errOAAI
errBercovici, Sivan; Geiger, Dan; Shlush, Liran; Skorecki, Karl; Templeton, Alan
err分享
err收藏
Estimation of flows in flow networks
errEUROPEAN JOURNAL OF OPERATIONAL RESEARCH
IF6
err2007-01-01
err7
PREAI
errZohar, Ron; Geiger, Dan
err分享
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A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2006-10-01
err113
errOAAI
errTopaz, Orit; Indelman, Margarita; Chefetz, Ilana; Geiger, Dan; Metzker, Aryeh; Altschuler, Yoram; Choder, Mordechai; Bercovich, Dani; Uitto, Jouni; Bergman, Reuven; Richard, Gabriele; Sprecher, Eli
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Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis:: Two allelic ectodermal dysplasias caused by dominant mutations in KRT14
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2006-10-01
err86
errOAAI
errLugassy, Jennie; Itin, Peter; Ishida-Yamamoto, Akemi; Holland, Kristen; Huson, Susan; Geiger, Dan; Hennies, Hans Christian; Indelman, Margarita; Bercovich, Dani; Uitto, Jouni; Bergman, Reuven; McGrath, John A.; Richard, Gabriele; Sprecher, Eli
err分享
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研究方向

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合作学者
合作期刊
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Markus M. Nöthen
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Jouni Uitto
H 指数: 114 · 论文数: 1.7K
M
Mary‐Claire King
H 指数: 109 · 论文数: 475
W
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