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1

Lynch Syndrome in high risk Ashkenazi Jews in Israel

Goldberg, Yael, Kedar, Inbal, Kariiv, Revital, Halpern, Naama, Plesser, Morasha, Hubert, Ayala, Kaduri, Luna, Sagi, Michal, Lerer, Israela, Abeliovich, Dvorah, Hamburger, Tamar, Nissan, Aviram, Goldsh

Journal:

Familial Cancer

Year:

2014

Language:

english

File:

PDF, 347 KB

english, 2014

2

ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia

Glaser, Benjamin, Blech, Ilana, Krakinovsky, Yocheved, Ekstein, Josef, Gillis, David, Mazor-Aronovitch, Kineret, Landau, Heddy, Abeliovich, Dvorah

Journal:

Genetics in Medicine

Year:

2011

Language:

english

File:

PDF, 143 KB

english, 2011

3

Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT

Israela Lerer, Michal Sagi, Esther Malamud, Haya Levi, Annick Raas-Rothschild, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 79 KB

english, 2000

4

Prevalence of myotonic dystrophy in Israeli Jewish communities: Inter-community variation and founder premutations

Reeval Segel, Shira Silverstein, Israela Lerer, Esther Kahana, Rachel Meir, Michal Sagi, Nelly Zilber, Amos D. Korczyn, Yehuda Shapira, Zohar Argov, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 74 KB

english, 2003

5

Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population

Josef Ekstein, Berish Y. Rubin, Sylvia L. Anderson, David A. Weinstein, Gideon Bach, Dvorah Abeliovich, Michael Webb, Neil Risch

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 48 KB

english, 2004

6

A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: A possible role of the Alu-polyA tail in the evolution of the deletion

Tieling Wang, Israela Lerer, Zehava Gueta, Michal Sagi, Luna Kadouri, Tamar Peretz, Dvorah Abeliovich

Journal:

Genes, Chromosomes and Cancer

Year:

2001

Language:

english

File:

PDF, 127 KB

english, 2001

7

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

Struewing, Jeffery P., Abeliovich, Dvorah, Peretz, Tamar, Avishai, Naaman, Kaback, Michael M., Collins, Francis S., Brody, Lawrence C.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 400 KB

1995

8

Genetic screening in patients with Retinoblastoma in Israel

Sagi, Michal, Frenkel, Avishag, Eilat, Avital, Weinberg, Naomi, Frenkel, Shahar, Pe’er, Jacob, Abeliovich, Dvorah, Lerer, Israela

Journal:

Familial Cancer

Year:

2015

Language:

english

File:

PDF, 1.10 MB

english, 2015

9

Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2

Shirly Bar-David, Israela Lerer, Chava Kimchi Sarfaty, Zully Gelman Kohan, Vardiella Meiner, Joel Zlotogora, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

1996

Language:

english

File:

PDF, 527 KB

english, 1996

10

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: Sex specific differences

Mitchell, John, Schinzel, Albert, Langlois, Sylvie, Gillessen-Kaesbach, Gabriele, Schuffenhauer, Simone, Michaelis, Ron, Abeliovich, Dvorah, Lerer, Isabel, Christian, Susan, Guitart, Miriam, McFadden,

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 509 KB

english, 1996

11

t(15;21)(q15;q22.1)pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring

Abeliovich, Dvorah, Dagan, Judith, Lerer, Israela, Silberstein, Shira, Katznelson, Mariassa Bat-Miriam, Frydman, Moshe

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 670 KB

english, 1996

12

TRISOMY 2: CONFINED PLACENTAL MOSAICISM IN A FETUS WITH INTRAUTERINE GROWTH RETARDATION

ILANA ARIEL, ISRAELA LERER, SIMCHA YAGEL, RACHEL COHEN, ZIVA BEN-NERIAH, DVORAH ABELIOVICH

Journal:

Prenatal Diagnosis

Year:

1997

Language:

english

File:

PDF, 272 KB

english, 1997

13

A large deletion mutation in the CFTR gene (3120+1Kbdel8.6Kb): A founder mutation in the Palestinian Arabs

Israela Lerer, Ayala Laufer-Cahana, Jacob R. Rivlin, Arie Augarten, Dvorah Abeliovich

Journal:

Year:

1999

Language:

english

File:

PDF, 80 KB

english, 1999

14

Cystic fibrosis mutations in Israeli Arab patients

Ayala Laufer-Cahana, Israela Lerer, Michal Sagi, Tamar Rachmilewitz-Minei, Chen Zamir, Jacob R. Rivlin, Dvorah Abeliovich

Journal:

Year:

1999

Language:

english

File:

PDF, 45 KB

english, 1999

15

The E148Q mutation in the MEFV gene: Is it a disease-causing mutation or a sequence variant?

Eldad Ben-Chetrit, Israela Lerer, Esther Malamud, Cecile Domingo, Dvorah Abeliovich

Journal:

Year:

2000

Language:

english

File:

PDF, 26 KB

english, 2000

16

Wiedemann-Beckwith syndrome: Further prenatal characterization of the condition

Orit Reish, Israela Lerer, Aliza Amiel, Eli Heyman, Arie Herman, Tzipora Dolfin, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 109 KB

english, 2002

17

Monosomy 21: A possible stepwise evolution of the karyotype

Dvorah Abeliovich, Rivka Carmi, Michael Karplus, Jacob Bar-Ziv, Maimon M. Cohen, R. L. Summitt

Journal:

American Journal of Medical Genetics Part A

Year:

1979

Language:

english

File:

PDF, 458 KB

english, 1979

18

Malformation syndrome associated with small extra chromosome

Rivka Carmi, Dvorah Abeliovich, Jacob Bar-Ziv, Michael Karplus, Maimon M. Cohen, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1980

Language:

english

File:

PDF, 404 KB

english, 1980

19

Familial midgut anomalies—a spectrum of defects due to the same cause?

Dr. Rivka Carmi, Dvorah Abeliovich, Leonardo Siplovich, Ehud Zmora, Jacob Bar-Ziv, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1981

Language:

english

File:

PDF, 211 KB

english, 1981

20

Genetics of cerebrotendinous xanthomatosis (CTX): An autosomal recessive trait with high gene frequency in Sephardim of Moroccan origin

Vladimir M. Berginer, Dr. Dvorah Abeliovich, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1981

Language:

english

File:

PDF, 387 KB

english, 1981

21

3:1 Meiotic disjunction in a mother with a balanced translocation, 46,XX,t(5,14)(p15;q13) resulting in tertiary trisomy and tertiary monosomy offspring

Dr. Dvorah Abeliovich, Pablo Yagupsky, Nava Bashan, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1982

Language:

english

File:

PDF, 439 KB

english, 1982

22

Radial ray aplasia and renal anomalies in father and son: A new syndrome

Shaul Sofer, Jacob Bar-Ziv, Dr. Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

1983

Language:

english

File:

PDF, 413 KB

english, 1983

23

A de novo translocation, 14q21q, with a microchromosome—14p21p

Dvorah Abeliovich, Miriam Katz, Michael Karplus, Rivka Carmi, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1985

Language:

english

File:

PDF, 266 KB

english, 1985

24

The translocation 11q;22q: A novel unbalanced karyotype

Dr. Dvorah Abeliovich, Rivka Carmi

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 82 KB

english, 1990

25

Isochromosome 18p in a mother and her child

Dr. Dvorah Abeliovich, Judith Dagan, Alina Levy, Avraham Steinberg, Joel Zlotogora

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 184 KB

english, 1993

26

Combined enzymatic and linkage analysis for heterozygote detection in Hunter syndrome: Identification of an apparent case of germinal mosaicism

Elena Ben Simon-Schiff, Gideon Bach, Joël Zlotogora, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 435 KB

english, 1993

27

Molecular diagnosis of Prader-Willi syndrome: Parent-of-origin dependent methylation sites and non-isotopic detection of (CA)n dinucleotide repeat polymorphisms

Israela Lerer, Vardiella Meiner, Iris Pashut-Layon, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 795 KB

english, 1994

28

Neurofibromatosis type I (NFI) in Israeli families: Linkage analysis as a diagnostic tool

Segal Elyakim, Israela Lerer, Joel Zlotogora, Michal Sagi, Zully Gelman-Kohan, Saul Merin, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 746 KB

english, 1994

29

Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females

Dvorah Abeliovich, Judith Dagan, Chava Kimchi-Sarfaty, Joel Zlotogora

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 377 KB

english, 1995

30

A patient with Prader–Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy

Marion Werner, Ziva Ben-Neriah, Shira silverstein, Israela Lerer, Yudith Dagan, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 147 KB

english, 2004

31

Myotonic dystrophy—no evidence for preferential transmission of the mutated allele: A prenatal analysis

Eran Zunz, Dvorah Abeliovich, Gabrielle J. Halpern, Nurit Magal, Mordechai Shohat

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 108 KB

english, 2004

32

Mutation spectrum in Jewish cystic fibrosis patients in Israel: Implication to carrier screening

Adina Quint, Israela Lerer, Michal Sagi, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 54 KB

english, 2005

33

Paternal isodisomy of chromosome 7 with cystic fibrosis and overgrowth

Fuad Fares, Miriam David, Aaron Lerner, Roni Diukman, Israela Lerer, Dvorah Abeliovich, Joseph Rivlin

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 186 KB

english, 2006

34

A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa

Eyal Banin, Liliana Mizrahi-Meissonnier, Ruhama Neis, Shira Silverstein, István Magyar, Dvorah Abeliovich, Ronald Roepman, Wolfgang Berger, Thomas Rosenberg, Dror Sharon

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 195 KB

english, 2007

35

Complex chromosomal rearrangement in a girl with psychomotor-retardation and a de novo inversion: inv(2)(p15;q24.2)

Einat Granot-Hershkovitz, Annick Raas-Rothschild, Ayala Frumkin, David Granot, Shira Silverstein, Dvorah Abeliovich

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 2.95 MB

english, 2011

36

A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews

Israela Lerer, Michal Sagi, Ziva Ben-Neriah, Tieling Wang, Haya Levi, Dvorah Abeliovich

Journal:

Year:

2001

Language:

english

File:

PDF, 92 KB

english, 2001

37

Polyglutamine repeat length in the AIB1 gene modifies breast cancer susceptibility in BRCA1 carriers

Luna Kadouri, Zsofia Kote-Jarai, Douglas F. Easton, Ayala Hubert, Rifat Hamoudi, Benjamin Glaser, Dvorah Abeliovich, Tamar Peretz, Rosalind A. Eeles

Journal:

International Journal of Cancer

Year:

2004

Language:

english

File:

PDF, 84 KB

english, 2004

38

Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes

Merav Bar, Eitan Friedman, Orit Jakobovitz, Gil Leibowitz, Israela Lerer, Dvorah Abeliovich, David J. Gross

Journal:

Clinical Endocrinology

Year:

1997

Language:

english

File:

PDF, 171 KB

english, 1997

39

Prenatal sex diagnosis: Testosterone and fsh levels in mid-trimester amniotic fluids

Dvorah Abeliovich, Joseph R Leiberman, Iris Teuerstein, Joseph Levy

Journal:

Prenatal Diagnosis

Year:

1984

Language:

english

File:

PDF, 359 KB

english, 1984

40

Prenatal ultrasonic diagnosis of radial-ray aplasia and renal anomalies (acro-renal syndrome)

Israel Meizner, Jacob Bar-Ziv, Yehiel Barki, Dvorah Abeliovich

Journal:

Prenatal Diagnosis

Year:

1986

Language:

english

File:

PDF, 208 KB

english, 1986

41

Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate

Shira Silverstein, Israela Lerer, Michal Sagi, Ayala Frumkin, Ziva Ben-Neriah, Dvorah Abeliovich

Journal:

Prenatal Diagnosis

Year:

2002

Language:

english

File:

PDF, 62 KB

english, 2002

42

Homozygosity ofMSH2c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I

Helen Toledano, Yael Goldberg, Inbal Kedar-Barnes, Hagit Baris, Rinnat M. Porat, Chen Shochat, Dani Bercovich, Eli Pikarsky, Israela Lerer, Isaac Yaniv, Dvorah Abeliovich, Tamar Peretz

Journal:

Familial Cancer

Year:

2009

Language:

english

File:

PDF, 644 KB

english, 2009

43

Absence of founderBRCA1andBRCA2mutations in coetaneous malignant melanoma patients of Ashkenazi origin

Luna Kadouri, Mark Temper, Tal Grenader, Dvorah Abeliovich, Tamar Hamburger, Tamar Peretz, Michal Lotem

Journal:

Familial Cancer

Year:

2009

Language:

english

File:

PDF, 155 KB

english, 2009

44

An Ashkenazi founder mutation in theMSH6gene leading to HNPCC

Yael Goldberg, Rinnat M. Porat, Inbal Kedar, Chen Shochat, Daliah Galinsky, Tamar Hamburger, Ayala Hubert, Hana Strul, Revital Kariiv, Liat Ben-Avi, Moran Savion, Eli Pikarsky, Dvorah Abeliovich, Dani

Journal:

Familial Cancer

Year:

2010

Language:

english

File:

PDF, 2.45 MB

english, 2010

45

X inactivation phenotype in carriers of Pelizaeus-Merzbacher disease: skewed in carriers of a duplication and random in carriers of point mutations

Woodward, Karen, Kirtland, Karen, Dlouhy, Stephen, Raskind, Wendy, Bird, Thomas, Malcolm, Sue, Abeliovich, Dvorah

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 201 KB

english, 2000

46

Reversed BCRABL rearrangement detected by FISH in Philadelphia negative chronic myelocytic leukemia

Dvorah Abeliovich, Orly Yehuda, Svetlana Krichevsky, Arnon Nagler, Susana Ben-Neriah, Marion Werner, Olga Ludkovsky, Dina Ben-Yehuda

Journal:

Cancer Genetics and Cytogenetics

Year:

1995

Language:

english

File:

PDF, 269 KB

english, 1995

47

Predominant 45,X,-Y karyotype in donor cells after allogeneic BMT: Cytogenetic and molecular analysis

Dvorah Abeliovich, Orly Yehuda, Arnon Nagler, Israela Lerer, Susana Ben-Neriah, Avraham Amar, Reuven Or

Journal:

Cancer Genetics and Cytogenetics

Year:

1996

Language:

english

File:

PDF, 902 KB

english, 1996

48

dup(10q) lacking α-satellite DNA in bone marrow cells of a patient with acute myeloid leukemia

Dvorah Abeliovich, Orly Yehuda, Susana Ben-Neriah, Yosef Kapelushnik, Dina Ben-Yehuda

Journal:

Cancer Genetics and Cytogenetics

Year:

1996

Language:

english

File:

PDF, 467 KB

english, 1996

49

The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3

Vered Molho-Pessach, Israela Lerer, Dvorah Abeliovich, Ziad Agha, Abdulasalam Abu Libdeh, Valentina Broshtilova, Orly Elpeleg, Abraham Zlotogorski

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 692 KB

english, 2008

50

Fluorescence in situ hybridization analysis of the cryptic t(12;21) (p13;q22) in childhood B-lineage acute lymphoblastic leukemia

Orly Yehuda-Gafni, Gabriel Cividalli, Ayala Abrahmov, Michael Weintrob, Susana Ben Neriah, Rachel Cohen, Dvorah Abeliovich

Journal:

Cancer Genetics and Cytogenetics

Year:

2002

Language:

english

File:

PDF, 69 KB

english, 2002

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